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<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J397100FP001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J397100FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J397100FP001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J397100FP003</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J397100FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J397100FP003">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J397100FP005</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>P005</fpage>
<lpage>P006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J397100FP005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J397100FP005">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of phenyl radicals with anthracene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bass</surname>
<given-names>K. C.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1</fpage>
<lpage>2</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of group V organometalloidal compounds. Part VI. Ring opening of β-propiolactone and of epoxides with dialkylamino(dimethyl)-arsines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000002</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Koketsu</surname>
<given-names>Jugo</given-names></name>
<name><surname>Ishii</surname>
<given-names>Yoshio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2</fpage>
<lpage>5</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000002">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000002">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of chlorocyclopentadienes with prop-2-ynyl bromide and bromoallene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000005</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alexander</surname>
<given-names>Richard</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>5</fpage>
<lpage>9</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000005">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidative dimerisations of natural rethrolones and related compounds with manganese dioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000009</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Ellis</surname>
<given-names>J. A.</given-names></name>
<name><surname>Gould</surname>
<given-names>R.</given-names></name>
<name><surname>Pattenden</surname>
<given-names>Gerald</given-names></name>
<name><surname>Elliott</surname>
<given-names>M.</given-names></name>
<name><surname>Janes</surname>
<given-names>N. F.</given-names></name>
<name><surname>Jeffs</surname>
<given-names>K. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>9</fpage>
<lpage>13</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000009">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000009">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>High resolution mass spectrometry. Part VIII. The fragmentation of ring A in some 3-oxo-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000013</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Midgley</surname>
<given-names>J. M.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>13</fpage>
<lpage>18</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000013">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000013">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>High resolution mass spectrometry. Part IX. 2-Spiro-2′-(1′,3′-dithian) derivatives of 3-oxo-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000019</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Midgley</surname>
<given-names>J. M.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
<name><surname>Smith</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>19</fpage>
<lpage>23</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000019">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000019">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Applications of high-potential quinones. Part IV. The mechanism of oxidation of 6-hydroxytetralins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000023</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Findlay</surname>
<given-names>J. W. A.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>23</fpage>
<lpage>29</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000023">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000023">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dalpanol, a new 6′-hydroxyrotenoid from a &lt;i&gt;Dalbergia&lt;/i&gt; species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000029</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adinarayana</surname>
<given-names>D.</given-names></name>
<name><surname>Radhakrishniah</surname>
<given-names>M.</given-names></name>
<name><surname>Rao</surname>
<given-names>J. Rajasekhara</given-names></name>
<name><surname>Campbell</surname>
<given-names>R.</given-names></name>
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>29</fpage>
<lpage>32</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000029">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000029">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dehydrogenation with mercuric acetate in the lupane series. Part IV. Acidic products of the reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adhikary</surname>
<given-names>S. P.</given-names></name>
<name><surname>Lawrie</surname>
<given-names>W.</given-names></name>
<name><surname>McLean</surname>
<given-names>J.</given-names></name>
<name><surname>Malik</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>32</fpage>
<lpage>36</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naturally occurring compounds related to phenalenone. Part I. The synthesis of lachnanthocarpone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laundon</surname>
<given-names>B.</given-names></name>
<name><surname>Morrison</surname>
<given-names>G. A.</given-names></name>
<name><surname>Brooks</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>36</fpage>
<lpage>40</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A convenient preparation of indenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lacy</surname>
<given-names>P. H.</given-names></name>
<name><surname>Smith</surname>
<given-names>D. C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>41</fpage>
<lpage>43</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Factors which affect the stability of aluminium hydride solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Sawdaye</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>44</fpage>
<lpage>46</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part XXXII. A simplified synthesis of bradykinin by use of the picolyl ester method</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000046</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schafer</surname>
<given-names>D. J.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
<name><surname>Elliott</surname>
<given-names>D. F.</given-names></name>
<name><surname>Wade</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>46</fpage>
<lpage>49</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000046">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000046">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part XXXIII. Synthesis of Val&lt;sup&gt;5&lt;/sup&gt;-angiotensin-II by the picolyl ester method</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000050</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garner</surname>
<given-names>R.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>50</fpage>
<lpage>53</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000050">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000050">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of 4a-alkoxy-1,2,3,4,4a,9b-hexahydro- and -1,2,3,4-tetra-hydro-benzofuro[3,2-&lt;i&gt;c&lt;/i&gt;]pyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cattanach</surname>
<given-names>C. J.</given-names></name>
<name><surname>Rees</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>53</fpage>
<lpage>60</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroheterocyclic compounds. Part XVIII. Reactions of heptafluoro-quinoline and -isoquinoline and pentafluoropyridine with hydrogen halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000061</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Hole</surname>
<given-names>M.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
<name><surname>Thorpe</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>61</fpage>
<lpage>67</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000061">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000061">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organometallic reactions. Part XIX. Some reactions of aldehydes with aminotin compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Kennedy</surname>
<given-names>John D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>68</fpage>
<lpage>73</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of 1-amino-8-hydroxynaphthalene-3,6-disulphonic acid and its &lt;i&gt;N&lt;/i&gt;-acyl and &lt;i&gt;N&lt;/i&gt;-&lt;i&gt;s&lt;/i&gt;-triazinyl derivatives with cyanuric chloride and 6-substituted 2,4-dichloro-&lt;i&gt;s&lt;/i&gt;-triazines. Formation of &lt;i&gt;O&lt;/i&gt;-&lt;i&gt;s&lt;/i&gt;-triazinyl derivatives and &lt;i&gt;peri&lt;/i&gt;-O-&lt;b&gt;→&lt;/b&gt; N-&lt;i&gt;s&lt;/i&gt;-triazinyl rearrangements</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Budziarek</surname>
<given-names>Richard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>74</fpage>
<lpage>80</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of pyrazoline formation from the reactions of substituted hydrazines and Mannich bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000080</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Houlihan</surname>
<given-names>(Miss) S. A.</given-names></name>
<name><surname>Fenton</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>80</fpage>
<lpage>86</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000080">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000080">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isoxazolin-5-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000086</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sarlo</surname>
<given-names>Francesco De</given-names></name>
<name><surname>Dini</surname>
<given-names>Giuliano</given-names></name>
<name><surname>Lacrimini</surname>
<given-names>Pasquale</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>86</fpage>
<lpage>89</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000086">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000086">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Valence-bond isomer chemistry. Part II. Diels–Alder reactions of hexafluorobicyclo[2,2,0]hexa-2,5-diene : pyrrole as a diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlow</surname>
<given-names>M. G.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Hubbard</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>90</fpage>
<lpage>95</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Curvularin. Part VII. Some acylations of 3,5-dihydroxytoluene and its dimethyl ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000095</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Munro</surname>
<given-names>H. D.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
<name><surname>Templeton</surname>
<given-names>Richard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>95</fpage>
<lpage>98</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000095">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000095">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Derivatives of 2-amino-2-deoxy-D-gulose: synthetic and conformational studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horner</surname>
<given-names>M. W.</given-names></name>
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Richardson</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>99</fpage>
<lpage>102</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thiazolinium salts and their reactions with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000103</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>A. D.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>103</fpage>
<lpage>110</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000103">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000103">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biosynthesis of terpenes and steroids. Part III. Squalene cyclisation in the biosynthesis of triterpenoids; the biosynthesis of fern-9-ene in &lt;i&gt;Polypodium vulgare&lt;/i&gt; Linn</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000110</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Mellows</surname>
<given-names>G.</given-names></name>
<name><surname>Widdowson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>110</fpage>
<lpage>116</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000110">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000110">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Internuclear cyclisation. Part XXVI. Photolysis of 2-iodo-&lt;i&gt;N&lt;/i&gt;-methylbenzanilide in benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000116</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Jones</surname>
<given-names>G. H.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>116</fpage>
<lpage>122</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000116">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000116">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Schotten–Baumann benzoylation of 2,4,4-trimethyl-1-pyrroline-1-oxide: a re-investigation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gutteridge</surname>
<given-names>N. J. A.</given-names></name>
<name><surname>Dales</surname>
<given-names>J. R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>122</fpage>
<lpage>125</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 6,8-disubstituted purines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000126</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Giner-Sorolla</surname>
<given-names>A.</given-names></name>
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>126</fpage>
<lpage>128</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000126">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000126">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vilsmeier reaction on 6-methylpurine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Giner-Sorolla</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>128</fpage>
<lpage>132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenothiazynes: preparation of 2- and 3-tertiary aminophenothiazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000132</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>132</fpage>
<lpage>137</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000132">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000132">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of &lt;i&gt;ortho&lt;/i&gt;-benzoquinones. Part IV. Addition of primary aromatic amines to 1,2-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000138</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Smith</surname>
<given-names>P. I.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>138</fpage>
<lpage>140</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000138">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000138">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A stilbene amino-acid derivative as a thyroxine analogue</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000141</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>G.</given-names></name>
<name><surname>Wright</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>141</fpage>
<lpage>142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000141">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000141">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituted stilbenes as potential chemotherapeutic agents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000143</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>W.</given-names></name>
<name><surname>Holland</surname>
<given-names>D.</given-names></name>
<name><surname>Jones</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>143</fpage>
<lpage>145</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000143">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000143">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3,4-Dihydro-4-oxo-2&lt;i&gt;H&lt;/i&gt;-1,3-benzoxazine-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000146</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fitton</surname>
<given-names>A. O.</given-names></name>
<name><surname>Ward</surname>
<given-names>M. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>146</fpage>
<lpage>149</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000146">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000146">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of the solanidane ring system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000149</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beisler</surname>
<given-names>J. A.</given-names></name>
<name><surname>Sato</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>149</fpage>
<lpage>152</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000149">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000149">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naturally occurring quinones. Part XVIII. New spinochromes from &lt;i&gt;Diadema antillarum, Spatangus purpureus&lt;/i&gt;, and &lt;i&gt;Temnopleurus toreumaticus&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000153</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mathieson</surname>
<given-names>J. W.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>153</fpage>
<lpage>160</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000153">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000153">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of organic peroxides. Part XVI. Amino-peroxides from autoxidation of imines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000160</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hawkins</surname>
<given-names>E. G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>160</fpage>
<lpage>166</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000160">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000160">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogeno-aromatic compounds. Part XVI. The preparation and reactions of polyhalogenophenyl- and polyhalogenopyridyl-hydrazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000167</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>I.</given-names></name>
<name><surname>Roberts</surname>
<given-names>S. M.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>167</fpage>
<lpage>174</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000167">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000167">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic uses of polyphosphoric acid. Part III. A ready synthesis of aromatic aldazines and ketazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000175</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mobbs</surname>
<given-names>D. B.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>175</fpage>
<lpage>178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000175">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000175">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of indole-2-carbaldehydes, 2-(2-aminoethyl)- and 2-(2-aminopropyl)-indoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000178</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhat</surname>
<given-names>G. A.</given-names></name>
<name><surname>Siddappa</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>178</fpage>
<lpage>181</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000178">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000178">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Condensed thiophen ring systems. Part V. Synthesis, reactions, and stability of 2-methyl- and 2-methylthio-3-benzo[&lt;i&gt;b&lt;/i&gt;]thienyl-lithium and related compounds.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dickinson</surname>
<given-names>R. P.</given-names></name>
<name><surname>Iddon</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>182</fpage>
<lpage>185</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of copper(I) acetylides with halogeno-acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000186</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Curtis</surname>
<given-names>R. F.</given-names></name>
<name><surname>Taylor</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>186</fpage>
<lpage>188</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000186">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000186">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on lactams. Part XIII. A position isomer of a penam (4-thia-1-aza-bicyclo[3,2,0]heptane)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000188</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bose</surname>
<given-names>Ajay K.</given-names></name>
<name><surname>Spiegelman</surname>
<given-names>G.</given-names></name>
<name><surname>Manhas</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>188</fpage>
<lpage>190</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000188">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000188">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A total synthesis of (±)-&lt;i&gt;O&lt;/i&gt;-methyl-14-methylpodocarpic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000190</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ghatak</surname>
<given-names>Usha Ranjan</given-names></name>
<name><surname>Chatterjee</surname>
<given-names>Nithar Ranjan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>190</fpage>
<lpage>196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000190">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000190">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of cyano-acetylenes. Part VIII. Claisen, amino-Claisen, and thio-Claisen rearrangements in the reactions of cyano-acetylenes with allyl alcohol, prop-2-ynol, allyl amines, and prop-2-enethiol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000196</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sasaki</surname>
<given-names>Tadashi</given-names></name>
<name><surname>Kojima</surname>
<given-names>Atsuyuki</given-names></name>
<name><surname>Ohta</surname>
<given-names>Masafumi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>196</fpage>
<lpage>200</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000196">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000196">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The stereochemistry of organometallic compounds. Part IX. Sodium borohydride reduction of oxymercury compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000200</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>G. A.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
<name><surname>Chambers</surname>
<given-names>V. M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>200</fpage>
<lpage>204</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000200">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000200">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lythraceous alkaloids. Part III. Synthesis of the product of dehydrogenation of dideoxy-&lt;i&gt;NO&lt;/i&gt;-dimethyl-lythranidine; the structure of lythranidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000205</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fujita</surname>
<given-names>E.</given-names></name>
<name><surname>Fuji</surname>
<given-names>K.</given-names></name>
<name><surname>Tanaka</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>205</fpage>
<lpage>207</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000205">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000205">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Condensation of aromatic aldehydes with ethoxycarbonylacetohydrazide and cyanoacetohydrazide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000207</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Callaghan</surname>
<given-names>C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>207</fpage>
<lpage>210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000207">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000207">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organophosphorus intermediates. Part III. The base-catalysed addition of methyl phenylphosphinate, dimethyl phosphonate, and diphenylphosphine oxide to tetraphenylcyclopentadienone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000210</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gallagher</surname>
<given-names>M. J.</given-names></name>
<name><surname>Jenkins</surname>
<given-names>I. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>210</fpage>
<lpage>218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000210">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000210">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>4-Hydroxy-6-methylchromen-2-thione, and a sulphur analogue of dicoumarol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000218</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Frankham</surname>
<given-names>D. B.</given-names></name>
<name><surname>Hatam</surname>
<given-names>Natiq</given-names></name>
<name><surname>Hill</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>218</fpage>
<lpage>222</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000218">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000218">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazo-ketones with potential tumour-inhibitory properties derived from L-aspartic and L-glutamic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000223</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Liwschitz</surname>
<given-names>Y.</given-names></name>
<name><surname>Nemes</surname>
<given-names>E.</given-names></name>
<name><surname>Neiman</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>223</fpage>
<lpage>225</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000223">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000223">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation of pyrazoles from 1,3,4-oxadiazolium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Dando</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>225</fpage>
<lpage>229</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Potentially carcinogenic cyclopenta[&lt;i&gt;a&lt;/i&gt;]phenanthrenes. Part V. Synthesis of 15,16-dihydro-7-methylcyclopenta[&lt;i&gt;a&lt;/i&gt;]phenanthren-17-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coombs</surname>
<given-names>M. M.</given-names></name>
<name><surname>Jaitly</surname>
<given-names>(Mrs.) S. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>230</fpage>
<lpage>234</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ‘trimer’ and ‘pentamer’ from the polymerisation of thiophen by polyphosphoric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000234</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Curtis</surname>
<given-names>R. F.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. M.</given-names></name>
<name><surname>Thomas</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>234</fpage>
<lpage>238</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000234">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000234">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part XV. Hexahydro- and octahydro-quinazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000238</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Kobayashi</surname>
<given-names>Toshihiko</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>238</fpage>
<lpage>245</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000238">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000238">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conversion of gibberellin A&lt;sub&gt;13&lt;/sub&gt; into some δ-lactones related to gibberellin A&lt;sub&gt;15&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000245</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>B. E.</given-names></name>
<name><surname>Stewart</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>245</fpage>
<lpage>250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Dimroth rearrangement. Part XIII. The small effect of &lt;i&gt;p&lt;/i&gt;-substitution on rearrangement rates for 1,2-dihydro-2-imino-1-methyl-5-phenylpyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000250</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>England</surname>
<given-names>B. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>250</fpage>
<lpage>256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000250">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000250">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of the reactions of anhydrosulphites of α-hydroxycarboxylic acids. Part VI. Anhydrosulphite synthesis and characterisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000257</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackbourn</surname>
<given-names>G. P.</given-names></name>
<name><surname>Tighe</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>257</fpage>
<lpage>259</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000257">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000257">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azasteroids. Part VII. Synthesis of 7-hydroxy-2-methoxy-7,8,9,10-tetrahydrobenzo[&lt;i&gt;i&lt;/i&gt;]phenanthridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000259</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kessar</surname>
<given-names>S. V.</given-names></name>
<name><surname>Sobti</surname>
<given-names>A. K.</given-names></name>
<name><surname>Joshi</surname>
<given-names>G. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>259</fpage>
<lpage>261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000259">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000259">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azasteroids. Part VIII. Synthesis and stereochemistry of (±)-13-aza-18-norequilenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kessar</surname>
<given-names>S. V.</given-names></name>
<name><surname>Singh</surname>
<given-names>Manmehar</given-names></name>
<name><surname>Ahuja</surname>
<given-names>V. K.</given-names></name>
<name><surname>Lumb</surname>
<given-names>Ashok Kumar</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>262</fpage>
<lpage>265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azasteroids. Part IX. Synthesis of (±)-13-aza-15-thia-18-norequilenin and a study of Bischler–Napieralski cyclisation of &lt;i&gt;N&lt;/i&gt;-acyl-2-(1-naphthyl)ethylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000266</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kessar</surname>
<given-names>S. V.</given-names></name>
<name><surname>Jit</surname>
<given-names>Pawan</given-names></name>
<name><surname>Mundra</surname>
<given-names>K. P.</given-names></name>
<name><surname>Lumb</surname>
<given-names>Ashok Kumar</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>266</fpage>
<lpage>269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000266">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000266">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diels–Alder reaction of unsymmetrical dienes with unsymmetrical &lt;i&gt;p&lt;/i&gt;-benzoquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Clements</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>269</fpage>
<lpage>275</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diels–Alder reaction of unsymmetrical dienes with methyl acrylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Clements</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>275</fpage>
<lpage>279</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of some halogeno-acetones including 1-bromo-1-chloro-1-fluoroacetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000279</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrett</surname>
<given-names>G. C.</given-names></name>
<name><surname>Hall</surname>
<given-names>D. Muriel</given-names></name>
<name><surname>Hargreaves</surname>
<given-names>M. K.</given-names></name>
<name><surname>Modarai</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>279</fpage>
<lpage>282</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000279">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000279">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrochemical reactions of fluoro-compounds. Part II. The preparation of substituted fluoro-aromatic derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Doyle</surname>
<given-names>A. M.</given-names></name>
<name><surname>Pedler</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>282</fpage>
<lpage>288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free-radical reactions of halogenated bridged polycyclic compounds. Part XI. Application of the Cristol–Firth reaction to some carboxylic acids containing a chloronorbornene ring system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000288</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Mason</surname>
<given-names>Patricia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>288</fpage>
<lpage>295</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000288">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000288">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free-radical reactions of halogenated bridged polycyclic compounds. Part XII. The formation of 1,2,3,5,5,6,6-heptachloronorborn-2-ene in the attempted chlorocarbonylation of 1,2,3,4,7,7-hexachloronorborn-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000295</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Mason</surname>
<given-names>Patricia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>295</fpage>
<lpage>296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000295">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000295">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acid-catalysed cleavage of the cyclopropane ring in some ketones of the carane series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000297</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fringuelli</surname>
<given-names>Francesco</given-names></name>
<name><surname>Taticchi</surname>
<given-names>Aldo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>297</fpage>
<lpage>299</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000297">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000297">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of organophosphorochloridates. Part I. Synthesis of &lt;i&gt;N&lt;/i&gt;-substituted phosphoramidic chlorides and acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000300</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Dewhurst</surname>
<given-names>B. B.</given-names></name>
<name><surname>Wakeford</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>300</fpage>
<lpage>303</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000300">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000300">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A novel bismethylene transfer to 2′-hydroxylated isoflavones by dimethylsulphoxonium methylide: study of the reaction and its products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000304</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Davies</surname>
<given-names>J. S.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>304</fpage>
<lpage>312</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000304">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000304">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conversion of labdadienols into pimara- and rosa-dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000312</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McCreadie</surname>
<given-names>T.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>312</fpage>
<lpage>316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000312">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000312">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A synthesis of rosenonolactone and deoxyrosenonolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McCreadie</surname>
<given-names>T.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
<name><surname>Allison</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>317</fpage>
<lpage>322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steric effects of methoxy-groups in some biphenyls derived from thebaine. Part I. Unbridged biphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>D. Muriel</given-names></name>
<name><surname>Manser</surname>
<given-names>W. W. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>323</fpage>
<lpage>328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and some reactions of 3-substituted 10b&lt;i&gt;H&lt;/i&gt;-oxazolo[3,2-&lt;i&gt;c&lt;/i&gt;][1,3]benzoxazine-2(3&lt;i&gt;H&lt;/i&gt;),5-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Block</surname>
<given-names>H.</given-names></name>
<name><surname>Faulkner</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>329</fpage>
<lpage>331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The biosynthesis of annuloline, a unique oxazole alkaloid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Horan</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>331</fpage>
<lpage>334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of phosphine sulphides with aryl-lithiums</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corfield</surname>
<given-names>J. R.</given-names></name>
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>334</fpage>
<lpage>336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Selective esterification, substitutions (&lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;1), and transformations of flavan-3,3′,4,4′,7-pentaols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000336</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Preez</surname>
<given-names>I. C. du</given-names></name>
<name><surname>Ferreira</surname>
<given-names>D.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>336</fpage>
<lpage>342</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000336">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000336">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of phosphorus compounds. Part XXIII. Preparation and reactions of several α-substituted vinylphosphonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000343</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schweizer</surname>
<given-names>Edward E.</given-names></name>
<name><surname>Wehman</surname>
<given-names>Anthony T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>343</fpage>
<lpage>346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000343">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000343">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Highly fluorinated heterocycles. Part IV. The fluorination of tetrachlorothiophen, thiophen, and tetrahydrothiophen over cobaltic and manganic trifluorides and over potassium tetrafluorocobaltate(III)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burdon</surname>
<given-names>J.</given-names></name>
<name><surname>Parsons</surname>
<given-names>I. W.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>346</fpage>
<lpage>352</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Highly fluorinated heterocycles. Part V. The preparation and some reactions of tetrafluorothiophen and some polyfluorothiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000352</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burdon</surname>
<given-names>J.</given-names></name>
<name><surname>Campbell</surname>
<given-names>J. G.</given-names></name>
<name><surname>Parsons</surname>
<given-names>I. W.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>352</fpage>
<lpage>355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000352">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000352">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Highly fluorinated heterocycles. Part VI. Fluorination and rearrangement of 1,4-dithian</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burdon</surname>
<given-names>J.</given-names></name>
<name><surname>Parsons</surname>
<given-names>I. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>355</fpage>
<lpage>359</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in the indole series. Part VI. Tetrahydropyrimido[3,4-&lt;i&gt;a&lt;/i&gt;]indoles and isotryptamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000359</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cattanach</surname>
<given-names>C. J.</given-names></name>
<name><surname>Cohen</surname>
<given-names>A.</given-names></name>
<name><surname>Heath-Brown</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>359</fpage>
<lpage>366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000359">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000359">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbene chemistry. Part II. Migration in fluoroalkylcarbenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000366</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atherton</surname>
<given-names>J. H.</given-names></name>
<name><surname>Fields</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>366</fpage>
<lpage>371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000366">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000366">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XIV. Novel tri- and tetra-cyclic compounds derived from a pteridine derivative by nucleophilic addition reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Yates</surname>
<given-names>F. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>371</fpage>
<lpage>374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XV. Synthesis and covalent hydration of pteridine-4-carboxylic acid, -4-carboxamide, and -4-carbonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Pendergast</surname>
<given-names>W.</given-names></name>
<name><surname>Yates</surname>
<given-names>F. S.</given-names></name>
<name><surname>Cunliffe</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>375</fpage>
<lpage>378</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of steroid A-ring lactones with Grignard reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000378</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Overnell</surname>
<given-names>J.</given-names></name>
<name><surname>Whitehurst</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>378</fpage>
<lpage>384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000378">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000378">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Allene cycloadditions. Part I. Reaction of tetrafluoroethylene with allenic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Warburton</surname>
<given-names>M. R.</given-names></name>
<name><surname>Wright</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>385</fpage>
<lpage>391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Allene cycloadditions. Part II. Reaction of a dialkylallene with unsymmetrical fluoro-olefins: evidence for a two-step [2 + 2] cycloaddition</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000391</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Wright</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>391</fpage>
<lpage>397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000391">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000391">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Further observations on the addition of tetrahalogeno-1,2-benzoquinone to cyclopentadienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000398</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Anderson</surname>
<given-names>D. T.</given-names></name>
<name><surname>Martin</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>398</fpage>
<lpage>400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000398">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000398">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis of some cyclopentadioxinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000400</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>400</fpage>
<lpage>404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000400">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000400">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carotenoids and related compounds. Part XXVIII. Synthesis of zeaxanthin, β-cryptoxanthin, and zeinoxanthin (α-cryptoxanthin)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Loeber</surname>
<given-names>D. E.</given-names></name>
<name><surname>Russell</surname>
<given-names>S. W.</given-names></name>
<name><surname>Toube</surname>
<given-names>T. P.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
<name><surname>Diment</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>404</fpage>
<lpage>408</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The action of amines on 1,3,4-oxadiazolium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000409</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Summers</surname>
<given-names>A. J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>409</fpage>
<lpage>414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000409">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000409">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;D&lt;/i&gt;-homo-steroids. Part III. The preparation of D-homoandrostane derivatives: a study of the reactions of steroidal C(17)-spiro-oxirans and their derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000414</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirk</surname>
<given-names>D. N.</given-names></name>
<name><surname>Wilson</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>414</fpage>
<lpage>424</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000414">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000414">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Simple pyrimidines. Part XII. Synthesis and methylation of some 2-amino-5-phenylpyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000425</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>England</surname>
<given-names>B. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>425</fpage>
<lpage>431</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000425">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000425">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thiophen derivatives. Part XX. Further studies on the Elbs reaction of aroylbenzo[&lt;i&gt;b&lt;/i&gt;]thiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marie</surname>
<given-names>Cl.</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>431</fpage>
<lpage>434</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic rearrangements. Part V. Transformations of 3,5-diacetyl-4-chloromethyl-1,4-dihydro-2,6-dimethylpyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000434</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allgrove</surname>
<given-names>R. C.</given-names></name>
<name><surname>Cort</surname>
<given-names>L. A.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>434</fpage>
<lpage>439</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000434">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000434">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermodynamically controlled enol acetylation of Δ&lt;sup&gt;4&lt;/sup&gt;-3-oxo-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000439</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Toft</surname>
<given-names>P.</given-names></name>
<name><surname>Liston</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>439</fpage>
<lpage>446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000439">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000439">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structures of the sulphones formed in the oxidation of the products of thiol addition to chloronorbornadienes and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Rowley</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>446</fpage>
<lpage>451</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinoxalines and related compounds. Part VIII. The reactions of quinoxaline-2(1&lt;i&gt;H&lt;/i&gt;)-ones and -2,3(1&lt;i&gt;H&lt;/i&gt;,4&lt;i&gt;H&lt;/i&gt;)-diones with hydrazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Rafiq</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>452</fpage>
<lpage>454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Action of base on non-enolisable carbonyl compounds. Part I. Cleavage of benzophenones and some related ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000455</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. G.</given-names></name>
<name><surname>Derenberg</surname>
<given-names>M.</given-names></name>
<name><surname>Hodge</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>455</fpage>
<lpage>460</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000455">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000455">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biosynthesis of phenols. Part XXII. Synthesis of 3-isopentyl-2,6-dimethoxyphenyl-(3,6-dimethoxy-2,4-dimethylphenyl)methane, a degradation product of arugosin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000460</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Catlin</surname>
<given-names>E. R.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>460</fpage>
<lpage>463</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000460">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000460">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thieno[2,3-&lt;i&gt;b&lt;/i&gt;][1]benzothiophen and thieno[3,2-&lt;i&gt;b&lt;/i&gt;][1]benzothiophen. Part II. Substitution reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Hughes</surname>
<given-names>C. G.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>463</fpage>
<lpage>468</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New synthesis of hexacene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000468</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Satchell</surname>
<given-names>M. P.</given-names></name>
<name><surname>Stacey</surname>
<given-names>B. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>468</fpage>
<lpage>469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000468">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000468">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 1,5-disubstituted naphthalenes with phthalic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Satchell</surname>
<given-names>M. P.</given-names></name>
<name><surname>Stacey</surname>
<given-names>B. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>469</fpage>
<lpage>474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrroles and related compounds. Part XV. Differential protection of pyrrole rings during porphyrin synthesis. Syntheses of mesoporphyrin-XI</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000474</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crook</surname>
<given-names>P. J.</given-names></name>
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>474</fpage>
<lpage>487</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000474">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000474">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrroles and related compounds. Part XVI. Synthesis of protoporphyrin-IX by the &lt;i&gt;a&lt;/i&gt;- and &lt;i&gt;b&lt;/i&gt;-oxobilane routes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000487</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carr</surname>
<given-names>R. P.</given-names></name>
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Sach</surname>
<given-names>G. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>487</fpage>
<lpage>502</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000487">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000487">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrroles and related compounds. Part XVII. Porphyrin synthesis through &lt;i&gt;b&lt;/i&gt;-bilenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000502</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Smith</surname>
<given-names>K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>502</fpage>
<lpage>509</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000502">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000502">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of hydroxyhydrolapachol and lapachol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pettit</surname>
<given-names>George R.</given-names></name>
<name><surname>Houghton</surname>
<given-names>Leonard E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>509</fpage>
<lpage>511</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of tris(dimethylamino)stibine with organic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000511</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Koketsu</surname>
<given-names>Jugo</given-names></name>
<name><surname>Ishii</surname>
<given-names>Yoshio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>511</fpage>
<lpage>513</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000511">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000511">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part X. Characterisation of the monamycins, members of a new family of cyclodepsipeptide antibiotics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>K.</given-names></name>
<name><surname>Davies</surname>
<given-names>J. S.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Morton</surname>
<given-names>R. B.</given-names></name>
<name><surname>Phillips</surname>
<given-names>D. A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>514</fpage>
<lpage>522</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part XI. (3&lt;i&gt;R&lt;/i&gt;,5&lt;i&gt;S&lt;/i&gt;)-5-chloropiperazic acid and (3&lt;i&gt;S&lt;/i&gt;,5&lt;i&gt;S&lt;/i&gt;)-5-hydroxypiperazic acid, products of hydrolysis of monamycin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000522</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Ogihara</surname>
<given-names>Y.</given-names></name>
<name><surname>Thomas</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>522</fpage>
<lpage>526</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000522">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000522">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part XII. The molecular structures of the monamycins, cyclodepsipeptide antibiotics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000526</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Morton</surname>
<given-names>R. B.</given-names></name>
<name><surname>Ogihara</surname>
<given-names>Y.</given-names></name>
<name><surname>Phillips</surname>
<given-names>D. A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>526</fpage>
<lpage>532</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000526">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000526">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions involving fluoride ion. Part III. Preparation, rearrangement, and hydrolysis of perfluoroisopropylpyridazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000532</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Cheburkov</surname>
<given-names>Yu. A.</given-names></name>
<name><surname>MacBride</surname>
<given-names>J. A. H.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>532</fpage>
<lpage>535</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000532">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000532">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation of nickel tetradehydrocorrin derivatives and the reduction of nickel 1,19-dimethyltetrahydrocorrin salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dicker</surname>
<given-names>I. D.</given-names></name>
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Pinnock</surname>
<given-names>H.</given-names></name>
<name><surname>Richardson</surname>
<given-names>K.</given-names></name>
<name><surname>Broek</surname>
<given-names>P. van den</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>536</fpage>
<lpage>547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Applications of high-potential quinones. Part V. Ring B oxidation in the podocarpic acid series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000547</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Findlay</surname>
<given-names>J. W. A.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>547</fpage>
<lpage>553</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000547">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000547">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated carbohydrates. Part XIV. The isomerisation of hex-2-enopyranosylpurine nucleoside derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000553</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferrier</surname>
<given-names>R. J.</given-names></name>
<name><surname>Ponpipom</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>553</fpage>
<lpage>559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000553">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000553">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated carbohydrates. Part XV. The synthesis of (3′-deoxyhex-2′-enopyranosyl)purine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000560</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferrier</surname>
<given-names>R. J.</given-names></name>
<name><surname>Ponpipom</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>560</fpage>
<lpage>562</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroarenes. Part XV. Diazo-oxides and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000562</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birchall</surname>
<given-names>J. M.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Nikokavouras</surname>
<given-names>J.</given-names></name>
<name><surname>Wilks</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>562</fpage>
<lpage>566</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000562">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000562">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryne chemistry. Part XXVIII. Some further cycloaddition reactions of tetrahalogenobenzynes generated from tetrahalogenoanthranilic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000567</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
<name><surname>Mason</surname>
<given-names>K. G.</given-names></name>
<name><surname>Sketchley</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>567</fpage>
<lpage>572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000567">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000567">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroids. Part XII. Westphalen-type rearrangements of 5α-hydroxy-4α-methyl- and 5α-hydroxy-4β-methyl-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000572</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. G. Ll.</given-names></name>
<name><surname>Marples</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>572</fpage>
<lpage>576</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroids. Part XIII. Boron trifluoride-catalysed rearrangement of 3β-acetoxy-5,6α-epoxy-19-methyl-5α-cholestane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000576</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Guest</surname>
<given-names>I. G.</given-names></name>
<name><surname>Marples</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>576</fpage>
<lpage>579</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000576">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000576">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Propyl homologue of tetrahydrocannabinol: its isolation from Cannabis, properties, and synthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000579</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gill</surname>
<given-names>E. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>579</fpage>
<lpage>582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An improvement of the Chugaev reaction with tertiary alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000582</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rutherford</surname>
<given-names>K. G.</given-names></name>
<name><surname>Ottenbrite</surname>
<given-names>R. M.</given-names></name>
<name><surname>Tang</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>582</fpage>
<lpage>583</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000582">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000582">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oximate anion as a powerful neighbouring group towards saturated carbon</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000584</article-id><contrib-group><contrib contrib-type="author">
<name><surname>MacConaill</surname>
<given-names>R. J.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>584</fpage>
<lpage>590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000584">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000584">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXI. A novel conversion of galanthamine into nivalidine under non-acidic conditions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Yamaki</surname>
<given-names>K.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Satoh</surname>
<given-names>F.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Hayasaka</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>590</fpage>
<lpage>592</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organophosphorus intermediates. Part IV. Formation of phenylphosphinidene in the decomposition of phenylphosphinic anhydride: mechanism for the thermal decomposition of monosubstituted phosphinic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gallagher</surname>
<given-names>M. J.</given-names></name>
<name><surname>Jenkins</surname>
<given-names>I. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>593</fpage>
<lpage>598</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Action of oxazol-5(4&lt;i&gt;H&lt;/i&gt;)-ones and of 4,5-dihydro-5-oxo-oxazolium perchlorates on enamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000598</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knowles</surname>
<given-names>A. M.</given-names></name>
<name><surname>Lawson</surname>
<given-names>Alexander</given-names></name>
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Newberry</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>598</fpage>
<lpage>603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000598">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000598">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polycyclic fluoroaromatic compounds. Part V. Some reactions of 1,2,3,4-tetrafluoronaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000604</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coe</surname>
<given-names>P. L.</given-names></name>
<name><surname>Pearl</surname>
<given-names>G. M.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>604</fpage>
<lpage>608</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000604">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000604">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;o&lt;/i&gt;-Quinonoid compounds. Part IV. 1,3-Diphenylinden-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000608</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holland</surname>
<given-names>J. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>608</fpage>
<lpage>612</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000608">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000608">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses of 6-deoxy-3-&lt;i&gt;O&lt;/i&gt;-methyl-D-gulose and 6-deoxy-3-&lt;i&gt;O&lt;/i&gt;-methyl-L-mannose(L-acofriose)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000613</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Robinson</surname>
<given-names>N.</given-names></name>
<name><surname>Webber</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>613</fpage>
<lpage>618</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000613">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000613">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rubratoxins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000619</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moss</surname>
<given-names>M. O.</given-names></name>
<name><surname>Robinson</surname>
<given-names>F. V.</given-names></name>
<name><surname>Wood</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>619</fpage>
<lpage>624</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000619">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000619">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent interactions in slow-inverting aziridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000624</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. J.</given-names></name>
<name><surname>Horwell</surname>
<given-names>D. C.</given-names></name>
<name><surname>Atkinson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>624</fpage>
<lpage>628</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000624">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000624">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biogenesis of xanthones in &lt;i&gt;Gentiana lutea&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gupta</surname>
<given-names>Padma</given-names></name>
<name><surname>Lewis</surname>
<given-names>John R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>629</fpage>
<lpage>631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Two new gibberellins, A&lt;sub&gt;24&lt;/sub&gt; and A&lt;sub&gt;25&lt;/sub&gt;, from &lt;i&gt;Gibberella fujikuroi&lt;/i&gt;; their isolation, structure, and correlation with gibberellins A&lt;sub&gt;13&lt;/sub&gt; and A&lt;sub&gt;15&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>D. M.</given-names></name>
<name><surname>MacMillan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>631</fpage>
<lpage>636</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction by dissolving metals. Part XVI. Reactions of some aromatic amines with metal–ammonia solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000637</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hutchinson</surname>
<given-names>E. G.</given-names></name>
<name><surname>Rao</surname>
<given-names>G. Subba</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>637</fpage>
<lpage>642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000637">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000637">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogenoaromatic compounds. Part XVII. Synthesis of arylpentachlorophenyl ketone imines and 2,4-diaryl-5,6,7,8-tetrachloroquinazolines by the reaction of pentachlorophenyl-lithium with nitriles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berry</surname>
<given-names>D. J.</given-names></name>
<name><surname>Wakefield</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>642</fpage>
<lpage>645</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroid conjugates. Part III. Syntheses of 19-oxygenated dehydro-&lt;i&gt;epi&lt;/i&gt;-androsterone sulphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000646</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rajagopalan</surname>
<given-names>M. S.</given-names></name>
<name><surname>Smith</surname>
<given-names>D. S. H.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>646</fpage>
<lpage>650</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000646">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000646">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear benzoylation of phenol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000650</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Smith</surname>
<given-names>G. H.</given-names></name>
<name><surname>Thorburn</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>650</fpage>
<lpage>652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000650">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000650">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkaloids of &lt;i&gt;Erythrina iysistemon&lt;/i&gt;. 11-Methoxyerythraline, a new alkaloid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Letcher</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>652</fpage>
<lpage>654</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proximity effects in diaryl derivatives. Part VI. Base-catalysed rearrangement of 2-(hydroxyamino)aryl aryl sulphones to 2-hydroxy-2′-(arylsulphonyl)azoxybenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000654</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grundon</surname>
<given-names>M. F.</given-names></name>
<name><surname>Maitland</surname>
<given-names>D. J.</given-names></name>
<name><surname>Matier</surname>
<given-names>W. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>654</fpage>
<lpage>661</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000654">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000654">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stobbe condensation with dimethyl glutarate. Syntheses of some polycyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000661</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatterjee</surname>
<given-names>Amareshwar</given-names></name>
<name><surname>Banerjee</surname>
<given-names>Somenath</given-names></name>
<name><surname>Sarker</surname>
<given-names>Asok K.</given-names></name>
<name><surname>Hazra</surname>
<given-names>Braja G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>661</fpage>
<lpage>667</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000661">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000661">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Allenes. Part XXI. The preparation of 1,1-dialkyl-3-iodoallenes and 1,1-dihalogenoallenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greaves</surname>
<given-names>P. M.</given-names></name>
<name><surname>Kalli</surname>
<given-names>M.</given-names></name>
<name><surname>Landor</surname>
<given-names>Phyllis D.</given-names></name>
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>667</fpage>
<lpage>670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of bicyclo[3,3,1]nona-3,7-diene-2,6-diones and bicyclo[3,3,1]-nona-3,6-diene-2,8-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000670</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knott</surname>
<given-names>P. A.</given-names></name>
<name><surname>Mellor</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>670</fpage>
<lpage>674</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000670">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000670">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XVI. Imidazo- and di-imidazo-pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000675</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Ramsden</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>675</fpage>
<lpage>678</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000675">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000675">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XVII. Some 2,3-dihydroimidazo-[1,2-&lt;i&gt;a&lt;/i&gt;]- and [1,2-&lt;i&gt;c&lt;/i&gt;]-pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000679</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Ramsden</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>679</fpage>
<lpage>683</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000679">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000679">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrochemical reactions. Part IX. Reduction of 2-acetylnaphthalene. Stereochemistry of the isomeric 2,3-di-(2-naphthyl)butane-2,3-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000683</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
<name><surname>Grimshaw</surname>
<given-names>J. T.</given-names></name>
<name><surname>Rea</surname>
<given-names>E. J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>683</fpage>
<lpage>685</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000683">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000683">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extractives from sporophores of some &lt;i&gt;Fomes&lt;/i&gt; species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000685</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Munro</surname>
<given-names>H. D.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>685</fpage>
<lpage>688</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000685">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000685">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sesquiterpenoids. Part XXXVII. Absolute configuration and conformation of zederone, a sesquiterpenoid of &lt;i&gt;Curcuma zedoaria&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000688</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hikino</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Tori</surname>
<given-names>Kazuo</given-names></name>
<name><surname>Horibe</surname>
<given-names>Isao</given-names></name>
<name><surname>Kuriyama</surname>
<given-names>Kaoru</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>688</fpage>
<lpage>691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000688">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000688">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition reactions of heterocyclic compounds. Part XLIII. Rotational isomerism of 5-oxidovinylphenanthridiniums: an investigation by variable temperature nuclear magnetic resonance spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000691</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Selby</surname>
<given-names>I. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>691</fpage>
<lpage>701</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000691">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000691">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spin traps. A cautionary note</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000701</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forrester</surname>
<given-names>A. R.</given-names></name>
<name><surname>Hepburn</surname>
<given-names>S. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>701</fpage>
<lpage>703</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000701">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000701">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and spectra of aminotetrazoles benzylated in the nucleus or in the side-chain</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000703</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Tobin</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>703</fpage>
<lpage>706</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000703">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000703">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of polyazaheterocyclic compounds. Part IV. Dimroth rearrangements of 4-substituted 5-amino-1-phenyl-1,2,3-triazoles and a synthesis of &lt;i&gt;v&lt;/i&gt;-triazolo[4,5-&lt;i&gt;d&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000706</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sutherland</surname>
<given-names>D. R.</given-names></name>
<name><surname>Tennant</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>706</fpage>
<lpage>713</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000706">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000706">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photoreduction of acetone by toluene and ethylbenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000714</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Singh</surname>
<given-names>Prithipal</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>714</fpage>
<lpage>716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000714">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000714">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1-Phenylnaphthalenes. Part VIII. Reactions of hydrazine and its derivatives with some five-membered ring anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>El-Newaihy</surname>
<given-names>M. F.</given-names></name>
<name><surname>Salem</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>716</fpage>
<lpage>721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000716">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical transformations. Part XXVIII. Aryl azides as potential photosensitive protecting groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Sammes</surname>
<given-names>P. G.</given-names></name>
<name><surname>Weingarten</surname>
<given-names>G. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>721</fpage>
<lpage>728</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000721">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical transformations. Part XXIX. Steric compression effects in the synthesis and reactions of 4-amino-5-methylphenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000729</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Sammes</surname>
<given-names>P. G.</given-names></name>
<name><surname>Weingarten</surname>
<given-names>G. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>729</fpage>
<lpage>736</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000729">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000729">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of 2-acyl- and 2-alkoxycarbonyl-octahydroindolo[2,3-&lt;i&gt;a&lt;/i&gt;]quinolizines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>M. S.</given-names></name>
<name><surname>Gaskell</surname>
<given-names>A. J.</given-names></name>
<name><surname>Joule</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>736</fpage>
<lpage>743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dienyl complexes of transition metals. Part V. Preparation and reactions of tricarbonyl(cycloheptatriene)manganese tetrafluoroborate and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000743</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haque</surname>
<given-names>F.</given-names></name>
<name><surname>Miller</surname>
<given-names>J.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Tripathi</surname>
<given-names>J. B. Pd.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>743</fpage>
<lpage>747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000743">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000743">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 1H-benzo[&lt;i&gt;de&lt;/i&gt;]cinnolines (1&lt;i&gt;H&lt;/i&gt;-1,2-diazaphenalenes)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lacy</surname>
<given-names>P. H.</given-names></name>
<name><surname>Smith</surname>
<given-names>D. C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>747</fpage>
<lpage>748</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and properties of bradykinin analogues: 1-deamino-, 9-decarboxy-, and 1-deamino-9-decarboxy-bradykinin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000748</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>W. H.</given-names></name>
<name><surname>Law</surname>
<given-names>H. D.</given-names></name>
<name><surname>Studer</surname>
<given-names>R. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>748</fpage>
<lpage>753</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000748">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000748">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of methyl vinyl ketone with 1-pyrrolidin-1-ylisobutene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000753</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>J. W.</given-names></name>
<name><surname>Myers</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>753</fpage>
<lpage>755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000753">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000753">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sesquiterpenes. Part IV. Synthesis of some tricyclo[5,4,0,0&lt;sup&gt;3,5&lt;/sup&gt;]undecanones and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fringuelli</surname>
<given-names>Francesco</given-names></name>
<name><surname>Taticchi</surname>
<given-names>Aldo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>756</fpage>
<lpage>758</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal rearrangement of &lt;i&gt;v&lt;/i&gt;-triazolo[1,5-&lt;i&gt;a&lt;/i&gt;]pyridine-3-acraldehydes into 3-methyl-5-(2-pyridyl)pyrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000759</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>L. S.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>759</fpage>
<lpage>762</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000759">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000759">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and proton magnetic resonance spectra of substituted biphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Hudson</surname>
<given-names>A. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>762</fpage>
<lpage>764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gamboge. Part V. Synthesis of 2′-isopropyl-5′-methylbiphenyl-2,4,6-triol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000765</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rigby</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>765</fpage>
<lpage>768</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000765">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000765">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fluorination of perchloro-2,5-dihydrofuran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000769</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feast</surname>
<given-names>W. J.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
<name><surname>Reeves</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>769</fpage>
<lpage>772</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000769">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000769">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 5-acetamido-2-acetylpiperidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000772</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>G. H.</given-names></name>
<name><surname>Rickard</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>772</fpage>
<lpage>776</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000772">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000772">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isothiazoles. Part XIII. Isothiazole sulphides and sulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000776</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caton</surname>
<given-names>M. P. L.</given-names></name>
<name><surname>Martin</surname>
<given-names>G. C. J.</given-names></name>
<name><surname>Pain</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>776</fpage>
<lpage>780</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000776">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000776">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridopyrimidines. Part VII. Reductive ring cleavage of pyrido[3,4-&lt;i&gt;d&lt;/i&gt;]pyrimidin-4(3&lt;i&gt;H&lt;/i&gt;)-ones with lithium aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000780</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gelling</surname>
<given-names>I. R.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>780</fpage>
<lpage>784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000780">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000780">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photo-oxidation of aryldihydropyrans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000784</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>784</fpage>
<lpage>788</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000784">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000784">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridine-catalysed condensation of citral with phloroglucinols, a novel reaction leading to tetracyclic bis-ethers and chromenes. Two-step synthesis of (±)-deoxybruceol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000788</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Ponsford</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>788</fpage>
<lpage>795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000788">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000788">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of cannabinoids by pyridine-catalysed citral–olivetol condensation: synthesis and structure of cannabicyclol, cannabichromen, (hashish extractives), citrylidene-cannabis, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000796</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Ponsford</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>796</fpage>
<lpage>804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000796">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000796">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridine-catalysed chromenylation of mono-chelated &lt;i&gt;meta&lt;/i&gt;-dihydric phenols with mono-, sesqui- and di-terpene aldehydes: synthesis of rubranine and flemingins A-, B- and C-methyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bandaranayake</surname>
<given-names>W. M.</given-names></name>
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>804</fpage>
<lpage>810</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3-Hydroxy-3-methyl-1,1-dimethoxybutane, a new reagent for dimethylchromenylation: synthesis of lonchocarpin, jacareubin, evodionol methyl ether, and other chromens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000811</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bandaranayake</surname>
<given-names>W. M.</given-names></name>
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>811</fpage>
<lpage>816</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000811">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000811">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Purines, pyrimidines, and imidazoles. Part XXXV. Potentiometric and spectroscopic studies of some imidazoles related to intermediates in the biosynthesis &lt;i&gt;de novo&lt;/i&gt; of purine nucleotides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000817</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Litchfield</surname>
<given-names>G. J.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>817</fpage>
<lpage>820</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000817">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000817">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of 2,3-epoxy-3-(2-nitrophenyl)propiophenone(2-nitrochalcone epoxide) with hydrogen chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000820</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sword</surname>
<given-names>Ian P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>820</fpage>
<lpage>823</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000820">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000820">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some oxidation reactions of monochloramine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000823</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jaffari</surname>
<given-names>G. A.</given-names></name>
<name><surname>Nunn</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>823</fpage>
<lpage>826</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000823">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000823">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereoselectivity in the addition of hydrogen chloride to cyclohex-1-enecarbonitrile: possible role of chlorine lone pair–nitrile &lt;i&gt;π&lt;/i&gt;-orbital pseudoallylic &lt;i&gt;A&lt;/i&gt;&lt;sup&gt;1, 3&lt;/sup&gt; interaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000827</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Balasubrahamanyam</surname>
<given-names>S. N.</given-names></name>
<name><surname>Balasubramanian</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>827</fpage>
<lpage>830</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000827">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000827">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical reactions of 16-oxo-oleanenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000830</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sugiyama</surname>
<given-names>Noboru</given-names></name>
<name><surname>Yamada</surname>
<given-names>Kazutoshi</given-names></name>
<name><surname>Aoyama</surname>
<given-names>Hiromu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>830</fpage>
<lpage>832</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000830">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000830">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Optical rotatory dispersion and circular dichroism. Part LXX. The circular dichroism of some less common amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fowden</surname>
<given-names>L.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
<name><surname>Thomas</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>833</fpage>
<lpage>840</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanisms of hydrogenation. Part VIII. Bis(pyridine)dimethylformamidedichlororhodium borohydride as a catalyst for homogeneous hydrogenation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000840</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abley</surname>
<given-names>P.</given-names></name>
<name><surname>Jardine</surname>
<given-names>I.</given-names></name>
<name><surname>McQuillin</surname>
<given-names>F. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>840</fpage>
<lpage>844</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000840">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000840">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanisms of hydrogenation. Part IX. Induced asymmetry in homogeneous hydrogenation at a rhodium complex by the use of optically active amide ligands</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000844</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abley</surname>
<given-names>P.</given-names></name>
<name><surname>McQuillin</surname>
<given-names>F. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>844</fpage>
<lpage>847</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000844">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000844">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and nuclear magnetic resonance spectra of substituted aminobornanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000847</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahmad</surname>
<given-names>(Mrs.) T.</given-names></name>
<name><surname>Anwar</surname>
<given-names>M. N.</given-names></name>
<name><surname>Martin-Smith</surname>
<given-names>M.</given-names></name>
<name><surname>Parfitt</surname>
<given-names>R. T.</given-names></name>
<name><surname>Smail</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>847</fpage>
<lpage>854</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000847">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000847">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Condensations of diketones with aromatic compounds. Part IV. Hexane-2,5-dione and pyrogallol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
<name><surname>Webster</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>855</fpage>
<lpage>858</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some conjugated 3-oxoergostane derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pelc</surname>
<given-names>B.</given-names></name>
<name><surname>Kodicek</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>859</fpage>
<lpage>860</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic quaternary ammonium salts. Part VII. The deoxygenation of pyrido[1,2-&lt;i&gt;a&lt;/i&gt;]pyrazinium 2-oxide salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000861</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adamson</surname>
<given-names>J.</given-names></name>
<name><surname>Glover</surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>861</fpage>
<lpage>866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000861">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000861">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and some properties of 1-(2-amino-oxyethyl)cytosines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000867</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Coe</surname>
<given-names>P. F.</given-names></name>
<name><surname>Green</surname>
<given-names>D. P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>867</fpage>
<lpage>869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000867">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000867">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of methyl 3-methyltridecanoate and 3,6-dimethyltridecanoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000870</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimwood</surname>
<given-names>P. D.</given-names></name>
<name><surname>Minnikin</surname>
<given-names>D. E.</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
<name><surname>Walker</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>870</fpage>
<lpage>871</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000870">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000870">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Derivatives of 2,4-dihydroxybenzophenone. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000871</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Head</surname>
<given-names>Frank S. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>871</fpage>
<lpage>874</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000871">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000871">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,3-Dipolar character of six-membered aromatic rings. Part I. 1-Methyl-3-oxidopyridinium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000874</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Takeuchi</surname>
<given-names>Yoshito</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>874</fpage>
<lpage>877</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000874">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000874">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,3-Dipolar character of six-membered aromatic rings. Part II. A novel route to tropones and tropolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000878</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Takeuchi</surname>
<given-names>Yoshito</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>878</fpage>
<lpage>880</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000878">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000878">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unusual behaviour of 2-methyladamantane during bromination</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000880</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alford</surname>
<given-names>J. R.</given-names></name>
<name><surname>Grant</surname>
<given-names>D.</given-names></name>
<name><surname>McKervey</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>880</fpage>
<lpage>883</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000880">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000880">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;trans&lt;/i&gt;-Cycloalkenes. Part I. (1&lt;i&gt;RS&lt;/i&gt;,2&lt;i&gt;RS&lt;/i&gt;)-&lt;i&gt;trans&lt;/i&gt;-Cyclo-oct-2-en-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000883</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
<name><surname>Wright</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>883</fpage>
<lpage>886</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000883">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000883">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;trans&lt;/i&gt;-Cycloalkenes. Part II. Application of the dioxolan olefin synthesis to the stereospecific formation of &lt;i&gt;trans&lt;/i&gt;-cyclo-octene derivatives. (1&lt;i&gt;SR&lt;/i&gt;,2&lt;i&gt;RS&lt;/i&gt;)-&lt;i&gt;trans&lt;/i&gt;-Cyclo-oct-2-en-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000886</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
<name><surname>Wright</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>886</fpage>
<lpage>891</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000886">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000886">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;trans&lt;/i&gt;-Cycloalkenes. Part III. Stereochemistry and mechanism of some reactions of diastereoisomeric 3-substituted &lt;i&gt;trans&lt;/i&gt;-cyclo-octenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000891</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
<name><surname>Wright</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>891</fpage>
<lpage>896</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000891">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000891">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free-radical reactions of halogenated bridged polycyclic compounds. Part XIII. The addition of hydrogen bromide to hexachloromethylenenorbornene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000896</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alexander</surname>
<given-names>Richard</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>896</fpage>
<lpage>898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000896">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000896">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation of optically active 3-aryl-1,4-dioxaspiro[4,5]decanes and their 2-oxo-derivatives; a study of the cotton effects associated with these compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000898</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Neilson</surname>
<given-names>Douglas G.</given-names></name>
<name><surname>Zakir</surname>
<given-names>U.</given-names></name>
<name><surname>Scrimgeour</surname>
<given-names>Charles M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>898</fpage>
<lpage>904</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000898">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000898">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The constitution of the aromatic diterpene cleistanthol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000904</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McGarry</surname>
<given-names>E. J.</given-names></name>
<name><surname>Pegel</surname>
<given-names>K. H.</given-names></name>
<name><surname>Phillips</surname>
<given-names>L.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>904</fpage>
<lpage>909</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000904">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000904">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinoline alkaloids. Part XI. A study of the Claisen rearrangement of the 3,3-dimethylallyl ether of 4-hydroxy-1-methyl-2-quinolone. Synthesis of ifflaiamine and the identification of a new alkaloid from &lt;i&gt;Flindersia ifflaiana&lt;/i&gt; F. Muell</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000910</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chamberlain</surname>
<given-names>T. R.</given-names></name>
<name><surname>Grundon</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>910</fpage>
<lpage>914</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000910">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000910">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pharmacologically active benzo[&lt;i&gt;b&lt;/i&gt;]thiophen derivatives. Part IX. Some 4- and 5-monosubstituted and 4,5-disubstituted amines and thiouronium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000915</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Clarke</surname>
<given-names>K.</given-names></name>
<name><surname>Gore</surname>
<given-names>B. A.</given-names></name>
<name><surname>Sharma</surname>
<given-names>K. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>915</fpage>
<lpage>919</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000915">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000915">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New ring systems derived from 4,5-diaminobenzo[&lt;i&gt;b&lt;/i&gt;]thiophen and its 3-methyl derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000919</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Clarke</surname>
<given-names>K.</given-names></name>
<name><surname>Sharma</surname>
<given-names>K. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>919</fpage>
<lpage>922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000919">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000919">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and biological evaluation of a conformationally flexible oestrogen analogue</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000922</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>922</fpage>
<lpage>925</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000922">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000922">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical isomerisation derivatives of decafluorocyclohexene and their reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Camaggi</surname>
<given-names>G.</given-names></name>
<name><surname>Gozzo</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>925</fpage>
<lpage>936</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diels–Alder reactions of polyfluorocyclohexa-1,3-dienes. Part III. Addition of alkynes, ethylene, and allene to 2&lt;i&gt;H&lt;/i&gt;,3&lt;i&gt;H&lt;/i&gt;-hexafluorocyclohexa-1,3-diene and reaction of some Diels–Alder adducts of octafluorocyclohexa-1,3-diene with lithium aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000937</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feast</surname>
<given-names>W. J.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
<name><surname>Weston</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>937</fpage>
<lpage>944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000937">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000937">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxymetalation. Part I. The peroxymercuration of monosubstituted ethylenes; a synthesis of secondary alkyl peroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000945</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>D. H.</given-names></name>
<name><surname>Bloodworth</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>945</fpage>
<lpage>949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000945">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000945">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical reduction of colupulone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000950</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Byrne</surname>
<given-names>E.</given-names></name>
<name><surname>Shaw</surname>
<given-names>S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>950</fpage>
<lpage>952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000950">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000950">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The oxidation of 5-arylsulphonamido-3,3-dimethyloxindoles and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000952</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>I.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Mensah</surname>
<given-names>I. A.</given-names></name>
<name><surname>Thoseby</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>952</fpage>
<lpage>955</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000952">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000952">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lichens and fungi. Part VII. Extractives from the lichen &lt;i&gt;Sticta mougeotiana&lt;/i&gt; var. dissecta del</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000955</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>R. E.</given-names></name>
<name><surname>Cumming</surname>
<given-names>Susan D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>955</fpage>
<lpage>960</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000955">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000955">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The gentamicin antibiotics. Part I. Structure and absolute stereochemistry of methyl garosaminide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000960</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>David J.</given-names></name>
<name><surname>Yudis</surname>
<given-names>Milton D.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
<name><surname>Prior</surname>
<given-names>(Miss) A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>960</fpage>
<lpage>963</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000960">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000960">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6a-Thiathiophthens and related compounds. Part II. Substitution reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000963</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beer</surname>
<given-names>R. J. S.</given-names></name>
<name><surname>Cartwright</surname>
<given-names>D.</given-names></name>
<name><surname>Gait</surname>
<given-names>R. J.</given-names></name>
<name><surname>Harris</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>963</fpage>
<lpage>966</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000963">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000963">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of isoquinolines from benzylaminoacetonitriles. Part I. Compounds prepared from veratrylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000967</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harcourt</surname>
<given-names>D. N.</given-names></name>
<name><surname>Waigh</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>967</fpage>
<lpage>970</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000967">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000967">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of cyclohexa-2,4-dienones with cyclopentadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000970</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bratby</surname>
<given-names>Dilys M.</given-names></name>
<name><surname>Fray</surname>
<given-names>G. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>970</fpage>
<lpage>974</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000970">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000970">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A new method for the preparation of Δ&lt;sup&gt;2&lt;/sup&gt;-isoxazolin-5-ones from the oximes of ketones having an α-hydrogen atom</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000974</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>Jonathan S.</given-names></name>
<name><surname>Beam</surname>
<given-names>Charles F.</given-names></name>
<name><surname>Hauser</surname>
<given-names>Charles R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>974</fpage>
<lpage>975</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000974">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000974">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The autoxidation of 2-(2-hydroxyphenyl)-3-methylindole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000976</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robinson</surname>
<given-names>B.</given-names></name>
<name><surname>Zubair</surname>
<given-names>M. Uppal</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>976</fpage>
<lpage>977</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000976">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000976">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive intermediates. Part XII. Attempts to form a benzyne–platinum complex</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000977</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Graveling</surname>
<given-names>F. J.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>977</fpage>
<lpage>980</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000977">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000977">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive intermediates. Part XIII. Benzocyclopropenones as intermediates in the oxidation of 3-aminobenzotriazin-4-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000981</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adamson</surname>
<given-names>J.</given-names></name>
<name><surname>Forster</surname>
<given-names>D. L.</given-names></name>
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>981</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000981">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000981">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive intermediates. Part XIV. Photochemistry of phthalimidoaziridines and related systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000988</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
<name><surname>Stanton</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>988</fpage>
<lpage>993</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000988">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000988">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidation, thermolysis, and photolysis of diarylsulphamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000993</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forster</surname>
<given-names>D. L.</given-names></name>
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>993</fpage>
<lpage>999</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000993">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000993">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of corydalactam</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710000999</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Ihara</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>999</fpage>
<lpage>1000</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710000999">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710000999">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Constituents of the higher fungi. Part X. The chromenols and chromanols of bovinone and a synthesis of hydroxy(methylthio)-quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001000</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaumont</surname>
<given-names>P. C.</given-names></name>
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1000</fpage>
<lpage>1004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001000">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001000">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An examination of the euphorbiaceae of Hong Kong. Part VIII. Lup-20(29)-ene-3α,23-diol, a new triterpene from &lt;i&gt;Glochidion macrophyllum&lt;/i&gt; benth</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hui (Miss) </surname>
<given-names>W. H.</given-names></name>
<name><surname>Lee</surname>
<given-names>W. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1004</fpage>
<lpage>1006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivity of mannich bases. Part XIV. Synthesis of phenylbenzoquinoline and styrylbenzoquinoline derivatives and their photoreactivity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andreani</surname>
<given-names>F.</given-names></name>
<name><surname>Andrisano</surname>
<given-names>R.</given-names></name>
<name><surname>Salvadori</surname>
<given-names>G.</given-names></name>
<name><surname>Tramontini</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1007</fpage>
<lpage>1013</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The resolution of 1-bromo-1-chloro-1-fluoroacetone and the preparation of (+)- and (–)-bromochlorofluoromethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001013</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hargreaves</surname>
<given-names>M. K.</given-names></name>
<name><surname>Modarai</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1013</fpage>
<lpage>1015</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001013">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001013">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triazoles. Part XII. Structure of 1,2,4-triazolinethiones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001016</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackman</surname>
<given-names>A. J.</given-names></name>
<name><surname>Polya</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1016</fpage>
<lpage>1018</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001016">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001016">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of a neoatisiranone, the enantiomer of a ketone obtained by the acid-catalysed rearrangement of isophyllocladene epoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gunn</surname>
<given-names>P. A.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Roy</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1018</fpage>
<lpage>1020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXII. Phenolic oxidative coupling of reticuline by use of various reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001021</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Kozuka</surname>
<given-names>A.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1021</fpage>
<lpage>1024</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001021">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001021">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXIII. A total synthesis of (–)(–)-&lt;i&gt;OO&lt;/i&gt;-dimethylcurine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001024</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Iida</surname>
<given-names>H.</given-names></name>
<name><surname>Sakurai</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1024</fpage>
<lpage>1029</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001024">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001024">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXIV. The formation of β-hydroxyreticuline by enzymic phenolic oxidation with homogenised &lt;i&gt;Papaver rhoeas&lt;/i&gt; and hydrogen peroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Takano</surname>
<given-names>S.</given-names></name>
<name><surname>Kobari</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1030</fpage>
<lpage>1031</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXV. Pschorr reactions of 1-(2-aminobenzyl)- and 1-(2-aminophenethyl)-1,2,3,4-tetrahydroisoquinolines (total synthesis of thalicsimidine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Takahashi</surname>
<given-names>K.</given-names></name>
<name><surname>Sugahara</surname>
<given-names>T.</given-names></name>
<name><surname>Koizumi</surname>
<given-names>M.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1032</fpage>
<lpage>1043</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXVI. Alternative total syntheses of galanthamine and &lt;i&gt;N&lt;/i&gt;-benzylgalanthamine iodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001043</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Seino</surname>
<given-names>C.</given-names></name>
<name><surname>Yamaki</surname>
<given-names>K.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Satoh</surname>
<given-names>F.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Hayasaka</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1043</fpage>
<lpage>1047</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001043">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001043">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzyne reaction. Part X. The benzyne reaction of &lt;i&gt;ortho&lt;/i&gt;-substituted halogenobenzenes with cyclohexanone in secondary cyclic amines or in organic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Noguchi</surname>
<given-names>S.</given-names></name>
<name><surname>Agata</surname>
<given-names>I.</given-names></name>
<name><surname>Aono</surname>
<given-names>T.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Hayasaka</surname>
<given-names>T.</given-names></name>
<name><surname>Kusama</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1047</fpage>
<lpage>1050</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzyne reaction. Part XI. Novel syntheses of 2-(3-substituted phenyl)cycloalkanones by the benzyne reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001051</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Hayasaka</surname>
<given-names>T.</given-names></name>
<name><surname>Kusama</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1051</fpage>
<lpage>1052</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001051">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001051">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCLXXXIX. An alternative synthesis of de-ethyldasycarpidone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Suzuki</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1053</fpage>
<lpage>1054</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some reactions of quinazoline-2,4(1&lt;i&gt;H&lt;/i&gt;,3&lt;i&gt;H&lt;/i&gt;)-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001055</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abdel-Megeid</surname>
<given-names>Farouk M. E.</given-names></name>
<name><surname>Elkaschef</surname>
<given-names>Mohamed A.-F.</given-names></name>
<name><surname>Mokhtar</surname>
<given-names>Kamal-Eldin M.</given-names></name>
<name><surname>Zaki</surname>
<given-names>Kamal-Eldin M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1055</fpage>
<lpage>1058</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001055">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001055">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of phosphines with acetylenes. Part XII. The mechanisms of 1,2-aryl migrations common to αβ-unsaturated phosphonium salts and “Wittig-type” phosphonium betaines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001059</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Richards</surname>
<given-names>Eileen M.</given-names></name>
<name><surname>Tebby</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1059</fpage>
<lpage>1063</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001059">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001059">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of phosphines with acetylenes. Part XIII. Ring expansion of dibenzophosph(III)ole derivatives to give dihydrodibenzophosphorin oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001064</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Richards</surname>
<given-names>Eileen M.</given-names></name>
<name><surname>Tebby</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1064</fpage>
<lpage>1066</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001064">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001064">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An examination of the rubiaceae of Hong Kong. Part VIII. The structure of spinosic acid A, a new triterpenoid sapogenin from &lt;i&gt;Randia spinosa&lt;/i&gt;(Thunb.) Poir.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001067</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Hui (Miss) </surname>
<given-names>W. H.</given-names></name>
<name><surname>Ho</surname>
<given-names>C. T.</given-names></name>
<name><surname>Yee</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1067</fpage>
<lpage>1069</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001067">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001067">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Components of the root of &lt;i&gt;Lindera strychnifolia&lt;/i&gt; Vill. Part XVIII. Neosericenyl acetate and dehydrolindestrenolide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001070</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tada</surname>
<given-names>H.</given-names></name>
<name><surname>Minato</surname>
<given-names>H.</given-names></name>
<name><surname>Takeda</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1070</fpage>
<lpage>1073</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001070">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001070">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of terpenes. Part XII. Oxidation of (+)-car-3-ene with t-butyl chromate and photolysis of the major oxidation product, (–)-car-3-en-5-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001073</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyle</surname>
<given-names>P. H.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Grayson</surname>
<given-names>D. H.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1073</fpage>
<lpage>1082</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001073">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001073">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sequential polypeptides. Part I. Use of mono-esters of catechol in the synthesis of sequential polypeptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001082</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cowell</surname>
<given-names>R. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1082</fpage>
<lpage>1090</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001082">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001082">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical modification of trehalose. Part V. The synthesis of mono- and di-epoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Munroe</surname>
<given-names>P. A.</given-names></name>
<name><surname>Richardson</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1090</fpage>
<lpage>1094</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homolytic reactions of perfluoroaromatic compounds. Part IV. Formation of pentafluorophenyl radicals from pentafluoroaniline, and their reactions with aromatic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001094</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oldham</surname>
<given-names>P. H.</given-names></name>
<name><surname>Williams</surname>
<given-names>Gareth H.</given-names></name>
<name><surname>Wilson</surname>
<given-names>Barbara A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1094</fpage>
<lpage>1098</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001094">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001094">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Friedel–Crafts reactions of n-alkenoic acids and ω-chloroalkanoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001098</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Whitfield</surname>
<given-names>G. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1098</fpage>
<lpage>1109</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001098">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001098">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carcinogenic nitrogen compounds. Part LXIX. Synthesis of polycyclic thiazoles from 4,5-dihydro-2-methylbenzothiazol-7(6&lt;i&gt;H&lt;/i&gt;)-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001109</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Croisy</surname>
<given-names>A.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
<name><surname>Martani</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1109</fpage>
<lpage>1111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001109">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001109">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lignans and related phenols. Part XI. Circular dichroism of apo-compounds of the arylnaphthalene class</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001111</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Harris</surname>
<given-names>J. A.</given-names></name>
<name><surname>Hulbert</surname>
<given-names>P. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1111</fpage>
<lpage>1114</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001111">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001111">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some reactions of arsenic ylides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001114</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
<name><surname>Walker</surname>
<given-names>Margaret A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1114</fpage>
<lpage>1117</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001114">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001114">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dimerisation of propene catalysed by transition-metal compounds and complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001117</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1117</fpage>
<lpage>1124</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001117">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001117">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Linear dimerisation of 1-olefins catalysed by complexes of nickel β-diketonates and aluminium alkyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001124</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. R.</given-names></name>
<name><surname>Symes</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1124</fpage>
<lpage>1130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001124">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001124">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological hydroxylation of steroids. Part II. Structural information and infrared spectrometry: carbonyl, perturbed methylene, and hydroxy-vibrations of steroidal ketones and alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001130</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boul</surname>
<given-names>A. D.</given-names></name>
<name><surname>Blunt</surname>
<given-names>J. W.</given-names></name>
<name><surname>Browne</surname>
<given-names>J. W.</given-names></name>
<name><surname>Kumar</surname>
<given-names>V.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Pinhey</surname>
<given-names>J. T.</given-names></name>
<name><surname>Thomas</surname>
<given-names>(Miss) V. E. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1130</fpage>
<lpage>1136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001130">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001130">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological hydroxylation of steroids. Part III. A convenient, microbiological route to 15-oxygenated 5α-androstanes.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blunt</surname>
<given-names>J. W.</given-names></name>
<name><surname>Clark</surname>
<given-names>I. M.</given-names></name>
<name><surname>Evans</surname>
<given-names>J. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Pinhey</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1136</fpage>
<lpage>1138</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermolysis of &lt;i&gt;N&lt;/i&gt;-&lt;i&gt;O&lt;/i&gt;-nitrophenyl- and &lt;i&gt;N&lt;/i&gt;-2,4-dinitrophenyl-α-amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001139</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goudie</surname>
<given-names>R. S.</given-names></name>
<name><surname>Preston</surname>
<given-names>P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1139</fpage>
<lpage>1142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001139">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001139">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biosynthesis of terpenes and steroids. Part IV. Specific hydride shifts in the biosynthesis of lanosterol and β-amyrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Mellows</surname>
<given-names>G.</given-names></name>
<name><surname>Widdowson</surname>
<given-names>D. A.</given-names></name>
<name><surname>Wright</surname>
<given-names>J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1142</fpage>
<lpage>1148</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transformation of the steroidal sapogenin side chain. Part II. A new method for the preparation of 16-alkylated-pregn-16-en-20-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001149</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Kulkarni</surname>
<given-names>Y. D.</given-names></name>
<name><surname>Sammes</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1149</fpage>
<lpage>1156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001149">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001149">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Natural acetylenes. Part XXXII. A synthesis of crepenynic acid (octadec-9-en-12-ynoic acid)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradshaw</surname>
<given-names>R. W.</given-names></name>
<name><surname>Day</surname>
<given-names>A. C.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Page</surname>
<given-names>C. B.</given-names></name>
<name><surname>Thaller</surname>
<given-names>V.</given-names></name>
<name><surname>Hodge</surname>
<given-names>R. A. Vere</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1156</fpage>
<lpage>1158</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel analgesics and molecular rearrangements in the morphine–thebaine group. Part XIX. Further Diels–Alder adducts of thebaine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001158</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>J. W.</given-names></name>
<name><surname>Readhead</surname>
<given-names>M. J.</given-names></name>
<name><surname>Selby</surname>
<given-names>I. A.</given-names></name>
<name><surname>Smith</surname>
<given-names>A. C. B.</given-names></name>
<name><surname>Young</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1158</fpage>
<lpage>1161</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001158">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001158">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel analgesics and molecular rearrangements in the morphine–thebaine group. Part XX. Reaction of 7β-cyano-6,14-&lt;i&gt;endo&lt;/i&gt;-etheno-7α-methyl-6,7,8,14-tetrahydrothebaine with phenylmagnesium bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001161</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>J. W.</given-names></name>
<name><surname>Readhead</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1161</fpage>
<lpage>1163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001161">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001161">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and mass spectra of 3-hydroxy-2,3,4,5-tetrahydro-1,5-benzoxazepine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coulson</surname>
<given-names>C. J.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R. H.</given-names></name>
<name><surname>Memel</surname>
<given-names>J.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1164</fpage>
<lpage>1167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of 3-hydroxy-2-naphthanilide with chloro-&lt;i&gt;s&lt;/i&gt;-triazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001167</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Budziarek</surname>
<given-names>Richard</given-names></name>
<name><surname>Hampson</surname>
<given-names>Philip</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1167</fpage>
<lpage>1170</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001167">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001167">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The formation of derivatives of bicyclo[3,2,1]octane in reactions between carbanions and quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001171</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Hindley</surname>
<given-names>Keith B.</given-names></name>
<name><surname>Houghton</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1171</fpage>
<lpage>1174</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The acid-catalysed addition of phenols and acetic acid to alkenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001174</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dalgleish</surname>
<given-names>D. T.</given-names></name>
<name><surname>Nonhebel</surname>
<given-names>D. C.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1174</fpage>
<lpage>1176</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001174">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001174">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluorocycloalkenes. Part IX. Reactions of 1&lt;i&gt;H&lt;/i&gt;,2&lt;i&gt;H&lt;/i&gt;-octafluorocyclohexene, -hexafluorocyclopentene and -tetrafluorocyclobutene with methanol under ionic conditions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001177</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clayton</surname>
<given-names>A. B.</given-names></name>
<name><surname>Collins</surname>
<given-names>D.</given-names></name>
<name><surname>Stephens</surname>
<given-names>R.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1177</fpage>
<lpage>1182</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001177">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001177">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluorocycloalkenes. Part X. Replacement reactions of octafluorocyclohexa-1,3- and -1,4-diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001183</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clayton</surname>
<given-names>A. B.</given-names></name>
<name><surname>Feast</surname>
<given-names>W. J.</given-names></name>
<name><surname>Sayers</surname>
<given-names>D. R.</given-names></name>
<name><surname>Stephens</surname>
<given-names>R.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1183</fpage>
<lpage>1189</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001183">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001183">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sporidesmins. Part XI. The reaction of triphenylphosphine with epipolythiodioxopiperazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001189</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Safe</surname>
<given-names>S.</given-names></name>
<name><surname>Taylor</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1189</fpage>
<lpage>1192</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001189">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001189">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic rearrangements. Part XIII. The conversion of a nitro-2,1-benzisoxazole into an acylbenzofurazan, and some unsuccessful rearrangements and oxygen transfer reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001193</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Fletcher</surname>
<given-names>I. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1193</fpage>
<lpage>1196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001193">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001193">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses with isoxazoles; the production of an isoxazolo[2,3-&lt;i&gt;a&lt;/i&gt;]pyridinium salt, and the photochemical conversion of isoxazole-3-carboxylates into oxazole-2-carboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001196</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Good</surname>
<given-names>R. H.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1196</fpage>
<lpage>1198</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001196">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001196">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydroxy-steroids. Part XVI. The preparation of 2,3-acetoxy-ketones and 2,3-diols from lupan-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001199</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boul</surname>
<given-names>A. D.</given-names></name>
<name><surname>Fairweather</surname>
<given-names>(Mrs.) P. M.</given-names></name>
<name><surname>Hall</surname>
<given-names>(Mrs.) J. M.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1199</fpage>
<lpage>1202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001199">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001199">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some &lt;i&gt;o&lt;/i&gt;-substituted &lt;i&gt;NN&lt;/i&gt;-dimethyl-2-halogeno-2-phenylethylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Clarke</surname>
<given-names>K.</given-names></name>
<name><surname>Harvey</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1202</fpage>
<lpage>1206</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>On the dealkylation of aromatic ethers with nitrous acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001206</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Gordon</surname>
<given-names>P. G.</given-names></name>
<name><surname>Hewitt</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1206</fpage>
<lpage>1210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001206">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001206">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation of a nitropyrido[3,4-&lt;i&gt;c&lt;/i&gt;]furoxan: 7-nitro[1,2,5]oxadiazolo-[3,4-&lt;i&gt;c&lt;/i&gt;]pyridine 3-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001211</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Heaton</surname>
<given-names>M. W.</given-names></name>
<name><surname>Murphy</surname>
<given-names>Miss J. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1211</fpage>
<lpage>1213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photo-acetalisation of α-aryloxyacetones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dirania</surname>
<given-names>M. K. M.</given-names></name>
<name><surname>Hill</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1213</fpage>
<lpage>1215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition of free radicals to unsaturated systems. Part XIX. The direction of radical addition ot 1,1,1-trifluorobut-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001216</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1216</fpage>
<lpage>1223</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001216">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001216">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogenoaromatic compounds. Part XVIII. Grignard reactions on pentachloropyridine 1-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001223</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Binns</surname>
<given-names>Falmai</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1223</fpage>
<lpage>1226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001223">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001223">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogenoaromatic compounds. Part XIX. Metal–halogen exchange reactions of n-butyl-lithium with tetrabromo-4-pyridyl and tetrachloro-2-pyridyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berry</surname>
<given-names>D. J.</given-names></name>
<name><surname>Wakefield</surname>
<given-names>B. J.</given-names></name>
<name><surname>Cook</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1227</fpage>
<lpage>1231</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive dyes. Part II. Synthesis and evaluation of dyes containing monochloropyrimidinium and monomethylthiopyrimidinium systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001231</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1231</fpage>
<lpage>1234</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001231">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001231">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance study of hindered rotation in &lt;i&gt;N&lt;/i&gt;-acyl derivatives of 5- and 6-membered &lt;i&gt;N&lt;/i&gt;-heterocycles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001234</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garner</surname>
<given-names>G. V.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1234</fpage>
<lpage>1236</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001234">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001234">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal rearrangement of 1-substituted 1&lt;i&gt;H&lt;/i&gt;-azepines to 6-amino-fulvenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001237</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mahendran</surname>
<given-names>M.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1237</fpage>
<lpage>1241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001237">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001237">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photoreduction of aromatic carbonyl compounds by tetra-n-butyltin and tri-n-butyltin hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimage</surname>
<given-names>D. R. G.</given-names></name>
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Lambeth</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1241</fpage>
<lpage>1244</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in the dithiocarbamate series. Part III. Mechanistic studies on the reaction of &lt;i&gt;N&lt;/i&gt;-benzylpiperidines and &lt;i&gt;N&lt;/i&gt;-benzylpyrrolidines with carbon disulphide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001245</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fitton</surname>
<given-names>A. O.</given-names></name>
<name><surname>Qutob</surname>
<given-names>M.</given-names></name>
<name><surname>Barber</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1245</fpage>
<lpage>1247</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mycological chemistry. Part XXVI. Total synthesis of (±)-&lt;i&gt;O&lt;/i&gt;-methylsterigmatocystin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001247</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rance</surname>
<given-names>Michael J.</given-names></name>
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1247</fpage>
<lpage>1252</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001247">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001247">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation of some linear polycyclic diquinones &lt;i&gt;via&lt;/i&gt; a novel dimerization</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001253</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>I.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Titman</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1253</fpage>
<lpage>1256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001253">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001253">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenanthro[9,10-&lt;i&gt;d&lt;/i&gt;]imidazole derivatives. The structure of Zincke's ‘phenanthraquinone imide anhydride’</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001256</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>J. W.</given-names></name>
<name><surname>Grinham</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1256</fpage>
<lpage>1259</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001256">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001256">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fusicoccin. Part I. The nature of the substituent groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001259</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrow</surname>
<given-names>K. D.</given-names></name>
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Chain</surname>
<given-names>Sir Ernst</given-names></name>
<name><surname>Conlay</surname>
<given-names>C.</given-names></name>
<name><surname>Smale</surname>
<given-names>T. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>R.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1259</fpage>
<lpage>1264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001259">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001259">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fusicoccin. Part II. The constitution of fusicoccin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrow</surname>
<given-names>K. D.</given-names></name>
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Chain</surname>
<given-names>Sir Ernst</given-names></name>
<name><surname>Ohnsorge</surname>
<given-names>U. F. W.</given-names></name>
<name><surname>Thomas</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1265</fpage>
<lpage>1274</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structures of 6β-bromoacetyl- and 6β-chloroacetyl-3,5α-cyclo-5α-cholestane (i-cholesteryl bromoacetate and chloroacetate)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>H. R.</given-names></name>
<name><surname>Hodgkin</surname>
<given-names>Dorothy Crowfoot</given-names></name>
<name><surname>Maslen</surname>
<given-names>E. N.</given-names></name>
<name><surname>Motherwell</surname>
<given-names>W. D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1275</fpage>
<lpage>1281</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluorocyclopentadienes. Part VII. Reaction of phenyl azide with 2,3,4,5,5,6-hexafluorotricyclo[5,2,1,0&lt;sup&gt;2, 6&lt;/sup&gt;]deca-3,8-diene and &lt;i&gt;endo&lt;/i&gt;-perfluorotricyclo[5,2,1,0&lt;sup&gt;2, 6&lt;/sup&gt;]deca-3,8-diene, and long-range &lt;sup&gt;19&lt;/sup&gt;F–&lt;sup&gt;19&lt;/sup&gt;F couplings in the product from the latter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Bridge</surname>
<given-names>M.</given-names></name>
<name><surname>Fields</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1282</fpage>
<lpage>1284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thieno[3,2-&lt;i&gt;c&lt;/i&gt;]pyridazine: synthesis and derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001285</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Poole</surname>
<given-names>A. J.</given-names></name>
<name><surname>Rose</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1285</fpage>
<lpage>1291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001285">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001285">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part X. Ring-contraction routes to some 8-methyl-&lt;i&gt;trans&lt;/i&gt;-perhydroindanones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001292</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawson</surname>
<given-names>T. M.</given-names></name>
<name><surname>Littlewood</surname>
<given-names>P. S.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
<name><surname>Medcalfe</surname>
<given-names>T.</given-names></name>
<name><surname>Moon</surname>
<given-names>M. W.</given-names></name>
<name><surname>Tomkins</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1292</fpage>
<lpage>1300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001292">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001292">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part XI. Improved routes to (&lt;i&gt;S&lt;/i&gt;)-3-hydroxymethyl-4-methylcyclohex-3-en-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001301</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dixon</surname>
<given-names>J.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
<name><surname>Siddiqui</surname>
<given-names>I. A.</given-names></name>
<name><surname>Tideswell</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1301</fpage>
<lpage>1305</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001301">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001301">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of unsaturated α-amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drinkwater</surname>
<given-names>D. J.</given-names></name>
<name><surname>Smith</surname>
<given-names>P. W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1305</fpage>
<lpage>1307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thieno[2,3-&lt;i&gt;b&lt;/i&gt;][1]benzothiophen and thieno[3,2-&lt;i&gt;b&lt;/i&gt;][1]benzothiophen. Part III. Substitution reactions of derivatives with substituents in the thiophen ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001308</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Hughes</surname>
<given-names>C. G.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1308</fpage>
<lpage>1313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mechanism of a steroidal aromatization reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001313</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hanson</surname>
<given-names>J. R.</given-names></name>
<name><surname>Organ</surname>
<given-names>T. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1313</fpage>
<lpage>1314</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isothiazoles. Part XIV. 5-Alkoxy- and 5-hydroxyisothiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stocks</surname>
<given-names>I. D. H.</given-names></name>
<name><surname>Waite</surname>
<given-names>J. A.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1314</fpage>
<lpage>1317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phytochemical examination of the lichen, &lt;i&gt;Lecanora rupicola&lt;/i&gt;(L.) Zahlbr</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001318</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Devlin</surname>
<given-names>J. P.</given-names></name>
<name><surname>Falshaw</surname>
<given-names>C. P.</given-names></name>
<name><surname>Ollis</surname>
<given-names>W. D.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1318</fpage>
<lpage>1323</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001318">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001318">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of sordidone and thiophanic acid, two chlorine-containing lichen metabolites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001324</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arshad</surname>
<given-names>M.</given-names></name>
<name><surname>Devlin</surname>
<given-names>J. P.</given-names></name>
<name><surname>Ollis</surname>
<given-names>W. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1324</fpage>
<lpage>1326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001324">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001324">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The behaviour of quaternary salts under reduced pressure. Part I. Improvement in yield during Hofmann elimination</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Archer</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1327</fpage>
<lpage>1329</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The behaviour of quaternary salts under reduced pressure. Part II. Decomposition of the &lt;i&gt;N&lt;/i&gt;-methylammonium hydroxides of benzyl-, dibenzyl-, and diphenylmethyl-amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Archer</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1329</fpage>
<lpage>1331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extractives from Guttiferae. Part XIX. The isolation and structure of two benzophenones, six xanthones and two biflavonoids from the heartwood of &lt;i&gt;Allanblackia floribunda&lt;/i&gt; Oliver</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001332</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Locksley</surname>
<given-names>H. D.</given-names></name>
<name><surname>Murray</surname>
<given-names>I. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1332</fpage>
<lpage>1340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroarenes. Part XVI. A convenient synthesis of pentafluorobenzonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001341</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birchall</surname>
<given-names>J. M.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Jones</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1341</fpage>
<lpage>1342</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001341">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001341">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroarenes. Part XVII. Some reactions of pentafluorobenzonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001343</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birchall</surname>
<given-names>J. M.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Jones</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1343</fpage>
<lpage>1348</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001343">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001343">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of polynuclear heterocycles. Part III. Imidazo[4,5-&lt;i&gt;f&lt;/i&gt;]benzofuroxans and -furazans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001348</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Perera</surname>
<given-names>R. C.</given-names></name>
<name><surname>Smalley</surname>
<given-names>R. K.</given-names></name>
<name><surname>Rogerson</surname>
<given-names>L. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1348</fpage>
<lpage>1354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001348">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001348">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dihydrobenzimidazole chemistry. Part V. The reaction of quaternised dihydrobenzimidazoles with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001354</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grantham</surname>
<given-names>R. K.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1354</fpage>
<lpage>1356</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001354">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001354">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of formation of benzimidazoles by oxidation of &lt;i&gt;o&lt;/i&gt;-acylamino-&lt;i&gt;NN&lt;/i&gt;-dialkylanilines with peroxy-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001356</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1356</fpage>
<lpage>1357</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001356">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001356">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part XI. Reaction of αβ-unsaturated acids and acid chlorides with imines. Synthesis of 2-oxotetrahydropyridines and 2-oxo-octahydroquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001358</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1358</fpage>
<lpage>1362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001358">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001358">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A synthesis of 2-&lt;i&gt;O&lt;/i&gt;-methyl-D-lyxose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001363</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Mofti</surname>
<given-names>A. M.</given-names></name>
<name><surname>Al-Radhi</surname>
<given-names>A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1363</fpage>
<lpage>1364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001363">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001363">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on ferrocene derivatives. Part X. Reaction of acetylferrocene with methylmagnesium iodide and of ferrocenyl alcohols with Grignard reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001365</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Stanley</surname>
<given-names>P.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>R. G.</given-names></name>
<name><surname>Thomson</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1365</fpage>
<lpage>1369</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001365">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001365">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ozonation of tertiary aromatic amines. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001369</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kerr</surname>
<given-names>G. H.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1369</fpage>
<lpage>1374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001369">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001369">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituted oxindoles. Part IV. 3-Alkylation of 1-methylindol-2(3&lt;i&gt;H&lt;/i&gt;)-one (1-methyloxindole)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Daisley</surname>
<given-names>R. W.</given-names></name>
<name><surname>Walker</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1375</fpage>
<lpage>1379</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of terminal &lt;i&gt;N&lt;/i&gt;-thiobenzoyl peptides by use of 4-substituted 2-phenylthiazol-5(4&lt;i&gt;H&lt;/i&gt;)-ones as acylating agents for amino-acids and peptides. Optically-active 4-substituted 2-phenylthiazol-5(4&lt;i&gt;H&lt;/i&gt;)-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrett</surname>
<given-names>G. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1380</fpage>
<lpage>1384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic nitro-compounds. Studies of the amination of 9-nitrophenanthrene and of the mononitrobiphenylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>J. W.</given-names></name>
<name><surname>Grinham</surname>
<given-names>A. R.</given-names></name>
<name><surname>Whitaker</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1384</fpage>
<lpage>1386</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dioxolan-4-ones and their structures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001386</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cort</surname>
<given-names>L. A.</given-names></name>
<name><surname>Stewart</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1386</fpage>
<lpage>1389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001386">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001386">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of santonene. Part VI. The chemistry of pyrosantonin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001389</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Rane</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1389</fpage>
<lpage>1392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001389">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001389">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of quinones with aromatic ethers. Part I. Polyalkoxydibenzo[&lt;i&gt;fg,op&lt;/i&gt;]naphthacene-1,8-quinones from chloranil and 3,3′,4,4′-tetra-alkoxybiphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001393</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
<name><surname>Webster</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1393</fpage>
<lpage>1397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001393">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001393">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of quinones with aromatic ethers. Part II. Polyalkoxytriphenylenes and -dibenzo[&lt;i&gt;fg,op&lt;/i&gt;]naphthacene-1,10-quinones from chloranil and &lt;i&gt;o&lt;/i&gt;-dialkoxybenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
<name><surname>Webster</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1397</fpage>
<lpage>1401</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of &lt;i&gt;o&lt;/i&gt;-benzoquinones with cyclopentadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Gosden</surname>
<given-names>A. F.</given-names></name>
<name><surname>Leslie</surname>
<given-names>V. J.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1401</fpage>
<lpage>1414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Diels–Alder reactions of &lt;i&gt;o&lt;/i&gt;-benzoquinones with acyclic dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001414</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Bignold</surname>
<given-names>A. J.</given-names></name>
<name><surname>Gosden</surname>
<given-names>A. F.</given-names></name>
<name><surname>Leslie</surname>
<given-names>V. J.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1414</fpage>
<lpage>1422</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001414">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001414">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of tetrachloro- and tetrabromo-&lt;i&gt;o&lt;/i&gt;-benzoquinone with acyclic dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001423</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Leslie</surname>
<given-names>V. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1423</fpage>
<lpage>1429</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001423">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001423">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of some &lt;i&gt;ortho&lt;/i&gt;-naphthoquinones with 2,3-dimethylbutadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001429</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1429</fpage>
<lpage>1437</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001429">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001429">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The circular dichroism of the &lt;i&gt;n&lt;/i&gt;&lt;b&gt;→&lt;/b&gt;π* band of cyclic thionocarbonates. Part I. The relationship between the magnitude and sign of the cotton effect, and the chirality of the five-membered thionocarbonate ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001438</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haines</surname>
<given-names>A. H.</given-names></name>
<name><surname>Jenkins</surname>
<given-names>C. S. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1438</fpage>
<lpage>1442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001438">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001438">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cytotoxic compounds. Part XII. Some 3-arylthiopropane-1,2-diols and 2-arylthiopropane-1,3-diols. Rearrangement of the 1,3-dimethanesulphonates to the 1,2-isomers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001442</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khan</surname>
<given-names>M. S.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1442</fpage>
<lpage>1447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001442">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001442">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cytotoxic compounds. Part XIII. Some 1-arylthiopropan-2-ols and 2-arylthiopropanols. Rearrangement of the primary methanesulphonates into the secondary isomers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001448</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khan</surname>
<given-names>M. S.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1448</fpage>
<lpage>1452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001448">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001448">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxymetallation. Part II. The t-butyl peroxymercuration and methoxymercuration of αβ-unsaturated ketones and esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001453</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bloodworth</surname>
<given-names>A. J.</given-names></name>
<name><surname>Bunce</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1453</fpage>
<lpage>1458</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001453">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001453">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>D-Glucose 1-phosphate formation by cyanogen-induced phosphorylation of D-glucose. Synthesis, mechanism, and application to other reducing sugars</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001459</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Degani</surname>
<given-names>Ch.</given-names></name>
<name><surname>Halmann</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1459</fpage>
<lpage>1465</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001459">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001459">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Circular dichroism of some optically active steroidal iodides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001466</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Coxon</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1466</fpage>
<lpage>1468</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001466">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001466">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroids. Part XIV. Transformations of 8α,9α- and 9α,11α-epoxylanostanes and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001468</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Guest</surname>
<given-names>I. G.</given-names></name>
<name><surname>Marples</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1468</fpage>
<lpage>1472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001468">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001468">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Keten. Part X. The reaction of dimethylketen with pyridine &lt;i&gt;N&lt;/i&gt;-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001472</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pratt</surname>
<given-names>R. N.</given-names></name>
<name><surname>Stokes</surname>
<given-names>D. P.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. A.</given-names></name>
<name><surname>Procter</surname>
<given-names>S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1472</fpage>
<lpage>1474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001472">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001472">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of organic peroxides. Part XVII. Hydroperoxides from cyclohexanone cyclohexylhydrazone and hydrazocyclohexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001474</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hawkins</surname>
<given-names>E. G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1474</fpage>
<lpage>1477</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001474">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001474">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Expansion of the ring of cyclododecanone by two and four carbon atoms</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001477</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Singh</surname>
<given-names>Prithipal</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1477</fpage>
<lpage>1481</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001477">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001477">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzopyrones. Part III. Synthesis and mass spectra of some oxopyranobenzoxazolecarboxylic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001482</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>G.</given-names></name>
<name><surname>Ellis</surname>
<given-names>G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1482</fpage>
<lpage>1484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001482">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001482">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thiacycloheptadeca-3,8,10,15-tetrayne and thiacycloheptadeca-2,8,10,16-tetrayne-4,15-diol. Attempted synthesis of thia[17]annulene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001485</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
<name><surname>Pellatt</surname>
<given-names>M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1485</fpage>
<lpage>1488</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001485">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001485">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The shikimate pathway. Part I. Introduction; preparation of stereospecifically labelled 2-deuterio-derivatives of 3-dehydroquinic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001489</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haslam</surname>
<given-names>E.</given-names></name>
<name><surname>Turner</surname>
<given-names>M. J.</given-names></name>
<name><surname>Sargent</surname>
<given-names>D.</given-names></name>
<name><surname>Thompson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1489</fpage>
<lpage>1495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001489">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001489">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The shikimate pathway. Part II. Conformational analysis of (–)-quinic acid and its derivatives by proton magnetic resonance spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001496</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haslam</surname>
<given-names>E.</given-names></name>
<name><surname>Turner</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1496</fpage>
<lpage>1500</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001496">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001496">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Purines, pyrimidines, and imidazoles. Part XXXVI. Carboxylation of some 5-aminoimidazoles and related compounds, including nucleosides and nucleotides, with potassium hydrogen carbonate in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001501</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cusack</surname>
<given-names>N. J.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
<name><surname>Litchfield</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1501</fpage>
<lpage>1507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001501">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001501">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conversion of aryl-&lt;i&gt;N&lt;/i&gt;-sulphohydroxylamines (&lt;i&gt;N&lt;/i&gt;-aryl-&lt;i&gt;N&lt;/i&gt;-hydroxysulphamic acids) to &lt;i&gt;o&lt;/i&gt;-aminoaryl hydrogen sulphates by acetone, and related reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001508</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Manson</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1508</fpage>
<lpage>1511</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001508">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001508">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of 5,10-epoxy-, 5,10-epithio-, 5,10-episeleno-, and 5,10-epitelluro-5,10-dihydroarsanthren</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001511</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kennard</surname>
<given-names>Olga</given-names></name>
<name><surname>Wampler</surname>
<given-names>D. L.</given-names></name>
<name><surname>Coppola</surname>
<given-names>J. C.</given-names></name>
<name><surname>Motherwell</surname>
<given-names>W. D. S.</given-names></name>
<name><surname>Mann</surname>
<given-names>F. G.</given-names></name>
<name><surname>Watson</surname>
<given-names>D. G.</given-names></name>
<name><surname>MacGillavry</surname>
<given-names>C. H.</given-names></name>
<name><surname>Stam</surname>
<given-names>C. H.</given-names></name>
<name><surname>Benci</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1511</fpage>
<lpage>1515</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001511">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001511">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The acetolysis and benzolysis of some carbohydrate oxirans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001515</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Conn</surname>
<given-names>J.</given-names></name>
<name><surname>Edgar</surname>
<given-names>A. R.</given-names></name>
<name><surname>Fletcher</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1515</fpage>
<lpage>1521</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3,6-Dioxocyclohexa-1,4-diene-1,2,4,5-tetracarboxylic acid dianhydride, a strong electron acceptor</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001521</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hammond</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1521</fpage>
<lpage>1523</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001521">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001521">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Compounds related to biologically active steroids. 1,2,3,4,9,10-Hexahydro-6,7-dimethoxyphenanthrene-2-spirocyclohexan-2′-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Askam</surname>
<given-names>V.</given-names></name>
<name><surname>Jones</surname>
<given-names>(Miss) D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1524</fpage>
<lpage>1526</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and reactions of thiazolidino[3,2-&lt;i&gt;a&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001527</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>G. R.</given-names></name>
<name><surname>Dyson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1527</fpage>
<lpage>1529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001527">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001527">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular reactions. Part IX. Stereochemistry and mechanism of the rearrangement of acetylenic esters of sulphinic and sulphenic acids to allenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001530</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>Geraldine</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1530</fpage>
<lpage>1535</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001530">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001530">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridazines. Part II. Reaction of polychloropyridazines with trimethylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fenton</surname>
<given-names>R. S.</given-names></name>
<name><surname>Landquist</surname>
<given-names>J. K.</given-names></name>
<name><surname>Meek</surname>
<given-names>Miss S. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1536</fpage>
<lpage>1539</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New metabolites of &lt;i&gt;Gibberella fujikuroi&lt;/i&gt;. Part XVII. The partial synthesis of gibberellin A&lt;sub&gt;15&lt;/sub&gt; norketone from 7-hydroxykaurenolide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001539</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>B. E.</given-names></name>
<name><surname>Gatfield</surname>
<given-names>I. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1539</fpage>
<lpage>1541</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001539">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001539">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fulvenes and thermochromic ethylenes. Part LIX. The reaction of diphenylcyclopropenone with cyanoacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001541</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Agranat</surname>
<given-names>Israel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1541</fpage>
<lpage>1542</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001541">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001541">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic polyfluoro-compounds. Part XLVII. The reactions of pentafluorophenyl-lithium with halogeno-olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001542</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Callander</surname>
<given-names>D. D.</given-names></name>
<name><surname>Coe</surname>
<given-names>P. L.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
<name><surname>Terrell</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1542</fpage>
<lpage>1547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001542">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001542">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diels–Alder reactions of polyfluorocyclohexa-1,3-dienes. Part IV. Addition of alkynes to 1&lt;i&gt;H&lt;/i&gt;,2&lt;i&gt;H&lt;/i&gt;-hexafluorocyclohexa-1,3-diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001547</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feast</surname>
<given-names>W. J.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
<name><surname>Weston</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1547</fpage>
<lpage>1549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001547">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001547">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in ferrocene derivatives. Part XI. Synthesis of some ferrocenyldihalogenocyclopropanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001550</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>R. G.</given-names></name>
<name><surname>Thomson</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1550</fpage>
<lpage>1554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in ferrocene derivatives. Part XII. Synthesis of ferrocenyl-1,2- and 1,3-dienes from some dibromo(ferrocenyl)cyclopropanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>R. G.</given-names></name>
<name><surname>Thomson</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1554</fpage>
<lpage>1557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in ferrocene derivatives. Part XIII. Synthesis and rearrangement of ferrocenylbicyclopropyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001558</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>R. G.</given-names></name>
<name><surname>Thomson</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1558</fpage>
<lpage>1563</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001558">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001558">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in ferrocene derivatives. Part XIV. Solvolytic reactions of some ferrocenydihalogenocyclopropanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001563</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>R. G.</given-names></name>
<name><surname>Thomson</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1563</fpage>
<lpage>1567</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001563">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001563">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A simple preparation of 1α,2α-epoxy-3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001568</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pelc</surname>
<given-names>B.</given-names></name>
<name><surname>Kodicek</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1568</fpage>
<lpage>1568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001568">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001568">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triterpenoids. Part VII. Photoisomerisation of 11-oxo-12-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001569</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Finucane</surname>
<given-names>B. W.</given-names></name>
<name><surname>Thomson</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1569</fpage>
<lpage>1570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001569">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001569">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterogeneous reactions of copper(II) chloride with toluene, &lt;i&gt;p&lt;/i&gt;-xylene, and mesitylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001571</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cummings</surname>
<given-names>C. A.</given-names></name>
<name><surname>Milner</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1571</fpage>
<lpage>1572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001571">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001571">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Optical rotatory dispersion and circular dichroism. Part LXXI. Low temperature circular dichroism of some tertiary carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001572</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mose</surname>
<given-names>W. P.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1572</fpage>
<lpage>1577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The deamination of pyranose amines. Part I. Equatorial amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001578</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kin</surname>
<given-names>N. M. K. Ng Ying</given-names></name>
<name><surname>Williams</surname>
<given-names>J. M.</given-names></name>
<name><surname>Horsington</surname>
<given-names>Mrs. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1578</fpage>
<lpage>1583</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001578">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001578">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance evidence regarding the stereochemistry of some cyanoindanylidene compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001583</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bahl</surname>
<given-names>A. K.</given-names></name>
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1583</fpage>
<lpage>1585</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001583">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001583">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transition metal complexes of some compounds related to intermediates in the biosynthesis &lt;i&gt;de novo&lt;/i&gt; of purine nucleotides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001585</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mulligan</surname>
<given-names>L. A.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
<name><surname>Staples</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1585</fpage>
<lpage>1587</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001585">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001585">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of 6-trimethylammoniopurinides and their isomerisation to 3- and 9-methyl analogues of 6-dimethylaminopurines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001587</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiburis</surname>
<given-names>J.</given-names></name>
<name><surname>Lister</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1587</fpage>
<lpage>1589</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001587">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001587">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of picryl and toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl azides with alkylindolizines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Brown</surname>
<given-names>B. R.</given-names></name>
<name><surname>Churn</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1590</fpage>
<lpage>1591</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of cycloheptatriene with acyl halides in the presence of Lewis acids. A convenient synthesis of 1-acylcycloheptatrienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001592</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blair</surname>
<given-names>J. A.</given-names></name>
<name><surname>Tate</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1592</fpage>
<lpage>1596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001592">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001592">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thyroxine analogues: synthesis and nuclear magnetic resonance spectral studies of diphenylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001596</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mukherjee</surname>
<given-names>R.</given-names></name>
<name><surname>Block jun. </surname>
<given-names>Paul</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1596</fpage>
<lpage>1600</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001596">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001596">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polycyclic fluoroaromatic compounds. Part V. Nucleophilic replacement in decafluorophenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001601</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burdon</surname>
<given-names>J.</given-names></name>
<name><surname>Kane</surname>
<given-names>B. L.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1601</fpage>
<lpage>1604</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001601">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001601">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The biosynthesis of santiaguine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001604</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Creedon</surname>
<given-names>P. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1604</fpage>
<lpage>1606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001604">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001604">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 2,3-dihydro-4-methylphenalen-1-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001607</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>C.</given-names></name>
<name><surname>Waite</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1607</fpage>
<lpage>1609</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001607">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001607">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Purines, pyrimidines, and imidazoles. Part XXXVII. Some new syntheses of pyrazolo[3,4-&lt;i&gt;d&lt;/i&gt;]pyrimidines, including allopurinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001610</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hildick</surname>
<given-names>B. G.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1610</fpage>
<lpage>1613</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001610">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001610">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of &lt;i&gt;trans&lt;/i&gt;-1,2-dichloroethylene with phosphorus trichloride–oxygen: the direct formation of a phosphate derivative from an olefin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001613</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyce</surname>
<given-names>C. B. C.</given-names></name>
<name><surname>Webb</surname>
<given-names>Shirley B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1613</fpage>
<lpage>1615</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001613">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001613">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 1,4-dihydropyrimido[2,1-&lt;i&gt;c&lt;/i&gt;][1,2,4]triazin-6-ones involving a new ring expansion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001615</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dunwell</surname>
<given-names>D. W.</given-names></name>
<name><surname>Evans</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1615</fpage>
<lpage>1618</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001615">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001615">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Coumarins and related compounds. Part XIII. Synthesis of 2-oxonaphtho[1,2-&lt;i&gt;b&lt;/i&gt;]pyran-6-propionic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001618</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gupta</surname>
<given-names>Arun K. Das</given-names></name>
<name><surname>Chatterje</surname>
<given-names>Rabindra M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1618</fpage>
<lpage>1619</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001618">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001618">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of phosphines with acetylenes. Part XIV. Isomeric 1 : 2 adducts from triarylphosphines and dimethyl acetylenedicarboxylate. A cyclopentenylidenephosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001620</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waite</surname>
<given-names>N. E.</given-names></name>
<name><surname>Tebby</surname>
<given-names>John C.</given-names></name>
<name><surname>Ward</surname>
<given-names>R. S.</given-names></name>
<name><surname>Shaw</surname>
<given-names>M. A.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1620</fpage>
<lpage>1622</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001620">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001620">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metabolites of &lt;i&gt;Lasiodiplodia theobromae&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001623</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aldridge</surname>
<given-names>D. C.</given-names></name>
<name><surname>Galt</surname>
<given-names>(Mrs.) S.</given-names></name>
<name><surname>Giles</surname>
<given-names>(the late) D.</given-names></name>
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1623</fpage>
<lpage>1627</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001623">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001623">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nuclear alkylation of pyrazines by ketones and aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001627</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bramwell</surname>
<given-names>A. F.</given-names></name>
<name><surname>Payne</surname>
<given-names>L. S.</given-names></name>
<name><surname>Riezebos</surname>
<given-names>G.</given-names></name>
<name><surname>Ward</surname>
<given-names>P.</given-names></name>
<name><surname>Wells</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1627</fpage>
<lpage>1632</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001627">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001627">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A convenient synthesis of 3-furoic acid and 3-acetylfuran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001632</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ohlsen</surname>
<given-names>S. R.</given-names></name>
<name><surname>Turner</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1632</fpage>
<lpage>1633</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001632">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001632">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part XVIII. Syntheses of derivatives of 3,5-diacetamido-3,5-dideoxy-L-arabinose and 3,5-diacetamido-3,5-dideoxy-L-lyxose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001634</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Mofti</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1634</fpage>
<lpage>1638</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001634">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001634">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of &lt;i&gt;ortho&lt;/i&gt;-benzoquinones. Part V. Cycloaddition reactions of indane-5,6-quinone, 5,6,7,8-tetrahydro-2,3-naphthoquinone, and of 4,5-dimethyl-1,2-benzoquinone with cyclopenadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Smith</surname>
<given-names>P.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1638</fpage>
<lpage>1640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydroformylation of (+)(&lt;i&gt;S&lt;/i&gt;)-3-methylpent-1-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001640</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pino</surname>
<given-names>P.</given-names></name>
<name><surname>Pucci</surname>
<given-names>S.</given-names></name>
<name><surname>Piacenti</surname>
<given-names>F.</given-names></name>
<name><surname>Dell'Amico</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1640</fpage>
<lpage>1643</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis of the alkaloids (±)-fumaritine and fumariline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001644</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kishimoto</surname>
<given-names>Teiji</given-names></name>
<name><surname>Uyeo</surname>
<given-names>Shojiro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1644</fpage>
<lpage>1647</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001644">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001644">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deamination of amino alicyclic carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001647</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Ellam</surname>
<given-names>R. M.</given-names></name>
<name><surname>Mitra</surname>
<given-names>T. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1647</fpage>
<lpage>1651</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001647">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001647">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lythraceous alkaloids. Part IV. Structure and absolute configuration of lythranine, lythranidine, and lythramine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001651</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fujita</surname>
<given-names>E.</given-names></name>
<name><surname>Fuji</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1651</fpage>
<lpage>1653</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001651">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001651">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation of 2,2,6,6-tetramethylpiperidine and 2,2,5,5-tetramethylpyrrolidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001653</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berg</surname>
<given-names>S. S.</given-names></name>
<name><surname>Cowling</surname>
<given-names>D. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1653</fpage>
<lpage>1658</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of pyrazoles from the &lt;i&gt;C&lt;/i&gt;(α)&lt;i&gt;NN&lt;/i&gt;-trianion of hydrazones having an α-hydrogen atom</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001658</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beam</surname>
<given-names>Charles F.</given-names></name>
<name><surname>Foote</surname>
<given-names>Robert S.</given-names></name>
<name><surname>Hauser</surname>
<given-names>(the late) Charles R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1658</fpage>
<lpage>1660</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001658">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001658">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peroxides of elements other than carbon. Part XVII. The reaction of trialkylstibines and trialkylbismuthines with t-butyl hydroperoxide and with oxygen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001660</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Hook</surname>
<given-names>Simon C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1660</fpage>
<lpage>1665</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001660">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001660">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis of 2,2,3,3-tetramethyl-β-alanine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001665</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shadbolt</surname>
<given-names>R. S.</given-names></name>
<name><surname>Stephens</surname>
<given-names>F. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1665</fpage>
<lpage>1666</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001665">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001665">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tautomeric &lt;i&gt;N&lt;/i&gt;-substituted 2-phenacylisothiouronium bromides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shadbolt</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1667</fpage>
<lpage>1669</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The tautomerism of &lt;i&gt;N&lt;/i&gt;-methyl-2-phenacylthioimidazoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001669</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shadbolt</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1669</fpage>
<lpage>1671</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001669">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001669">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Optical rotatory dispersion and circular dichroism. Part LXXII. (2&lt;i&gt;R&lt;/i&gt;)-Mercaptopropionic acid and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001671</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
<name><surname>Thomas</surname>
<given-names>R. N.</given-names></name>
<name><surname>Rahman</surname>
<given-names>M. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1671</fpage>
<lpage>1676</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001671">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001671">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tautomeric forms and ionisation processes in xanthine and its &lt;i&gt;N&lt;/i&gt;-methyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001676</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lichtenberg</surname>
<given-names>D.</given-names></name>
<name><surname>Bergmann</surname>
<given-names>F.</given-names></name>
<name><surname>Neiman</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1676</fpage>
<lpage>1682</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001676">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001676">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosensitized decarboxylation of carboxylic acids by benzophenone and quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001682</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Steiner</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1682</fpage>
<lpage>1689</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001682">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001682">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in the flavin series. Part XVI. Alkylation and rearrangement reactions of dihydroalloxazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001689</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jefcoate</surname>
<given-names>C. R.</given-names></name>
<name><surname>Ghisla</surname>
<given-names>S.</given-names></name>
<name><surname>Hemmerich</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1689</fpage>
<lpage>1694</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001689">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001689">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naturally-occurring compounds related to phenalenone. Part II. The synthesis of haemocorin aglycone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001694</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laundon</surname>
<given-names>B.</given-names></name>
<name><surname>Morrison</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1694</fpage>
<lpage>1704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001694">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001694">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isomerism in arylsulphonylamidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001704</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Danilewicz</surname>
<given-names>J. C.</given-names></name>
<name><surname>Sewell</surname>
<given-names>M. J.</given-names></name>
<name><surname>Thurman</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1704</fpage>
<lpage>1707</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001704">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001704">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of some dicarbonyl compounds. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001708</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Ladwa</surname>
<given-names>P. H.</given-names></name>
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Ntamila</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1708</fpage>
<lpage>1711</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001708">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001708">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The circular dichroism of some 2,2′-bridged biphenyls. The absolute configuration of (+)-6,7-diphenyldibenzo[&lt;i&gt;e,g&lt;/i&gt;][1,4]diazocine-3,10-dicarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Insole</surname>
<given-names>Joan M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1712</fpage>
<lpage>1715</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tetranortriterpenoids and related substances. Part XIII. The constitution of grandifoliolenone, an &lt;i&gt;apo&lt;/i&gt;-tirucallol derivative from &lt;i&gt;Khaya grandifoliola&lt;/i&gt;(meliaceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001715</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connolly</surname>
<given-names>J. D.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1715</fpage>
<lpage>1718</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001715">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001715">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermolysis of &lt;i&gt;o&lt;/i&gt;-nitro- and 2,4-dinitro-phenoxyacetic acids and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001718</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goudie</surname>
<given-names>R. S.</given-names></name>
<name><surname>Preston</surname>
<given-names>P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1718</fpage>
<lpage>1721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001718">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001718">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polypeptides. Part XV. The synthesis and oxidation of some L-cysteinylpolyglycyl-L-cysteines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001722</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hardy</surname>
<given-names>P. M.</given-names></name>
<name><surname>Ridge</surname>
<given-names>B.</given-names></name>
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
<name><surname>Serrão</surname>
<given-names>F. O. dos S. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1722</fpage>
<lpage>1731</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001722">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001722">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical modification of trehalose. Part VI. The synthesis of analogues containing 2,2′-dideoxy-functions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001732</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Richardson</surname>
<given-names>A. C.</given-names></name>
<name><surname>Tarelli</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1732</fpage>
<lpage>1738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001732">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001732">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A simple preparation of tri-isopropylanisoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001738</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duck</surname>
<given-names>E. W.</given-names></name>
<name><surname>Locke</surname>
<given-names>J. M.</given-names></name>
<name><surname>Wallis</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1738</fpage>
<lpage>1740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001738">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001738">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on conformation and reactivity. Part IX. Stereochemical aspects of the Diels–Alder reaction of diethyl azodicarboxylate with steroid dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001741</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yoshizawa</surname>
<given-names>Junji</given-names></name>
<name><surname>Tomoeda</surname>
<given-names>Munemitsu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1741</fpage>
<lpage>1747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001741">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001741">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homolytic acylation of benzothiazole. A diagnostic criterion for the presence of acyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caronna</surname>
<given-names>T.</given-names></name>
<name><surname>Galli</surname>
<given-names>R.</given-names></name>
<name><surname>Malatesta</surname>
<given-names>V.</given-names></name>
<name><surname>Minisci</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1747</fpage>
<lpage>1750</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenol oxidation mechanisms. A search for phenoxylium intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001750</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewitt</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1750</fpage>
<lpage>1757</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001750">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001750">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The resolution of 2-chlorofluoren-9-ol and the preparation of (+)- and (–)-2,9-dichlorofluorene, (+)-9-bromo-2-chlorofluorene, and the corresponding racemic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001757</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Darby</surname>
<given-names>A. C.</given-names></name>
<name><surname>Hargreaves</surname>
<given-names>M. K.</given-names></name>
<name><surname>Lestas</surname>
<given-names>C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1757</fpage>
<lpage>1761</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001757">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001757">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton nuclear magnetic resonance spectra of phosphorus-containing esters with transition-metal ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001761</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Engel</surname>
<given-names>Robert</given-names></name>
<name><surname>Jung</surname>
<given-names>Alfred</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1761</fpage>
<lpage>1763</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001761">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001761">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ring-opening reactions of 7,7-dichlorobicyclo[3,2,0]hept-2-en-6-one and its conversion into methyl benzoate with methoxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001764</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brook</surname>
<given-names>P. R.</given-names></name>
<name><surname>Duke</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1764</fpage>
<lpage>1769</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001764">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001764">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organotin chemistry. Part IX. Functionally substituted metallostanoxanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001769</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Harrison</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1769</fpage>
<lpage>1771</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001769">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001769">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of tautomerism. Part II. Reactions of the pseudo-acid chloride of &lt;i&gt;o&lt;/i&gt;-benzoylbenzoic acid with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001772</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhatt</surname>
<given-names>M. V.</given-names></name>
<name><surname>Kamath</surname>
<given-names>K. M.</given-names></name>
<name><surname>Ravindranathan</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1772</fpage>
<lpage>1777</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001772">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001772">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidation of alkoxyphenols. Part XIX. Base-induced coupling of halogenophenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001777</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowman</surname>
<given-names>D. F.</given-names></name>
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1777</fpage>
<lpage>1788</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001777">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001777">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A galactan from onion (&lt;i&gt;Allium cepa&lt;/i&gt; Linn.) pectic substance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001788</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sen</surname>
<given-names>S. K.</given-names></name>
<name><surname>Chatterjee</surname>
<given-names>B. P.</given-names></name>
<name><surname>Rao</surname>
<given-names>C. V. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1788</fpage>
<lpage>1791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001788">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001788">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Total synthesis of &lt;i&gt;O&lt;/i&gt;-methylandrocymbine by a photo-Pschorr reaction and synthesis of thalifoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001792</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Koizumi</surname>
<given-names>M.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1792</fpage>
<lpage>1796</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001792">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001792">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCXCII. An alternative total synthesis of petaline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001796</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Kobari</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Fujihara</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1796</fpage>
<lpage>1800</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001796">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001796">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CCCXCIII. Synthesis of norerythrinadienone by phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001800</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Takahashi</surname>
<given-names>K.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1800</fpage>
<lpage>1803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001800">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001800">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation of indole derivatives by phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001803</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Seino</surname>
<given-names>C.</given-names></name>
<name><surname>Noguchi</surname>
<given-names>I.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Kohno</surname>
<given-names>T.</given-names></name>
<name><surname>Takano</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1803</fpage>
<lpage>1805</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001803">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001803">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclised products in the synthesis of 6-substituted phenanthridines by phenolic cyclisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001805</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Ishimaru</surname>
<given-names>H.</given-names></name>
<name><surname>Wakisaka</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1805</fpage>
<lpage>1808</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001805">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001805">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sesquiterpenes. Part V. Some tricyclic undecanols and related β-iso-propyldecalols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001809</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fringuelli</surname>
<given-names>Francesco</given-names></name>
<name><surname>Taticchi</surname>
<given-names>Aldo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1809</fpage>
<lpage>1812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001809">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001809">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part XVI. A stereospecific &lt;i&gt;cis&lt;/i&gt;-addition of the elements of nitromethane across a tetrasubstituted ethylenic double bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001812</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1812</fpage>
<lpage>1817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001812">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001812">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The rearrangement of &lt;i&gt;exo&lt;/i&gt;-2-bromobicyclo[2,2,1]heptane-1-carboxylic acid during reduction with lithium aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>MacMillan</surname>
<given-names>J.</given-names></name>
<name><surname>Pryce</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1818</fpage>
<lpage>1822</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Methylation reactions of 6-methylthio-8-phenylpurines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001822</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Neiman</surname>
<given-names>Z.</given-names></name>
<name><surname>Bergmann</surname>
<given-names>F.</given-names></name>
<name><surname>Lichtenberg</surname>
<given-names>D.</given-names></name>
<name><surname>Deutsch</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1822</fpage>
<lpage>1829</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001822">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001822">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part XII. Reaction of acid chlorides with cross-conjugated dienamines. Synthesis of γ-pyrones, dihydro-γ-pyrones and biphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001829</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Yoxall</surname>
<given-names>C. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1829</fpage>
<lpage>1833</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001829">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001829">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and thermal rearrangement of oxime thiocarbamates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>Barrington</given-names></name>
<name><surname>Searle</surname>
<given-names>R. J. G.</given-names></name>
<name><surname>Woodall</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1833</fpage>
<lpage>1835</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of phenylphosphonous acid with carbonyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>I. G. M.</given-names></name>
<name><surname>Raza</surname>
<given-names>S. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1836</fpage>
<lpage>1840</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic reactions in strong alkalis. Part V. Alkali fusion of epoxides and ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001840</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Shepherd</surname>
<given-names>I. S.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1840</fpage>
<lpage>1846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001840">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001840">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic reactions in strong alkalis. Part VI. Further studies on alkali fusion reactions of keto- and hydroxy-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001846</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Redshaw</surname>
<given-names>D. J.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1846</fpage>
<lpage>1850</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001846">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001846">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic reactions in strong alkalis. Part VII. Fission of unsaturated acids by alkali fusion in potassium deuterioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001851</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Radziwill</surname>
<given-names>A. N.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1851</fpage>
<lpage>1856</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001851">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001851">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The autoxidation of 9(10)-hydroxy-10(9)-oxo-octadecanoic acid in alkaline media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001857</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Shepherd</surname>
<given-names>I. S.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1857</fpage>
<lpage>1859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001857">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001857">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on intramolecular Friedel–Crafts cyclisation. Part II. Synthesis of 7-methoxy-8-methyl-1-tetralone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatterjee</surname>
<given-names>Amareshwar</given-names></name>
<name><surname>Banerjee</surname>
<given-names>Dilip</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1859</fpage>
<lpage>1862</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis of phenacyl-sulphonium and -ammonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001863</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laird</surname>
<given-names>T.</given-names></name>
<name><surname>Williams</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1863</fpage>
<lpage>1869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001863">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001863">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of group IV organometallic compounds. Part XXII. An extensive study on preparation of some oxadiazinones by the reaction of N-trimethylmetal(IV)dialkylamines with benzoyl isocyanate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001870</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Matsuda</surname>
<given-names>Isamu</given-names></name>
<name><surname>Itoh</surname>
<given-names>Kenji</given-names></name>
<name><surname>Ishii</surname>
<given-names>Yoshio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1870</fpage>
<lpage>1875</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001870">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001870">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of [1,4]benzoxazino[2,3-&lt;i&gt;b&lt;/i&gt;]phenoxazines and [1,4]benzothiazino[2,3-&lt;i&gt;b&lt;/i&gt;]phenothiazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001875</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mital</surname>
<given-names>R. L.</given-names></name>
<name><surname>Jain</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1875</fpage>
<lpage>1878</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001875">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001875">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Retinol analogues. Part I. Synthesis of acyclic analogues of retinoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001878</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Augustyn</surname>
<given-names>O. P. H.</given-names></name>
<name><surname>Wet</surname>
<given-names>P. de</given-names></name>
<name><surname>Garbers</surname>
<given-names>C. F.</given-names></name>
<name><surname>Lourens</surname>
<given-names>L. C. F.</given-names></name>
<name><surname>Neuland</surname>
<given-names>E.</given-names></name>
<name><surname>Schneider</surname>
<given-names>D. F.</given-names></name>
<name><surname>Steyn</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1878</fpage>
<lpage>1884</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001878">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001878">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lichens and fungi. Part VIII. 18α-Oleanane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001884</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>R. E.</given-names></name>
<name><surname>Ding</surname>
<given-names>H. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1884</fpage>
<lpage>1885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001884">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001884">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lichens and fungi. Part IX. 17α&lt;i&gt;H&lt;/i&gt;-hopane and 17α&lt;i&gt;H&lt;/i&gt;-moretane and their derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001885</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>R. E.</given-names></name>
<name><surname>Heng</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1885</fpage>
<lpage>1888</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001885">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001885">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrimidine reactions. Part XXII. The relative reactivities of some corresponding chloro-, bromo-, and iodo-pyrimidines in aminolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arantz</surname>
<given-names>B. W.</given-names></name>
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1889</fpage>
<lpage>1891</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation of 2-methylaminopyridine-3-carbaldehyde and the corresponding methylimine by ring-opening and ring-closing reactions of 3-cyano-1-methylpyridinium iodide in N-sodium hydroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001892</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blanch</surname>
<given-names>J. H.</given-names></name>
<name><surname>Fretheim</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1892</fpage>
<lpage>1895</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001892">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001892">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transformations in ring a of methyl glycyrrhetinate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Askam</surname>
<given-names>V.</given-names></name>
<name><surname>Bradley</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1895</fpage>
<lpage>1901</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Adducts from quinones and diazoalkanes. Part VIII. Further reactions of 2-methyl-1,4-naphthoquinone with carbanions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001902</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Houghton</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1902</fpage>
<lpage>1905</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001902">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001902">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Products from diborane reduction of αβ-unsaturated ketones: &lt;i&gt;trans&lt;/i&gt;-and &lt;i&gt;cis&lt;/i&gt;-1β-acetoxy-8aβ-methyl-Δ&lt;sup&gt;5&lt;/sup&gt;-octalin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001905</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schmitz</surname>
<given-names>Francis J.</given-names></name>
<name><surname>Peters</surname>
<given-names>C. Allan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1905</fpage>
<lpage>1907</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001905">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001905">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated carbohydrates. Part XVI. Isomerisation of allylic 4-azides and 4-thiocyanates and the subsequent synthesis of 2-acetamido-2-deoxyhexopyranoside derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001907</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferrier</surname>
<given-names>R. J.</given-names></name>
<name><surname>Vethaviyaser</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1907</fpage>
<lpage>1913</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001907">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001907">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogenoaromatic compounds. Part XX. Some reactions of decachlorobiphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001913</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Binns</surname>
<given-names>Falmai</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1913</fpage>
<lpage>1917</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001913">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001913">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Derivatives of 6-aminopenicillanic acid. Part X. A non-enzymic conversion of benzylpenicillin into semi-synthetic penicillins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001917</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fosker</surname>
<given-names>G. R.</given-names></name>
<name><surname>Hardy</surname>
<given-names>K. D.</given-names></name>
<name><surname>Nayler</surname>
<given-names>J. H. C.</given-names></name>
<name><surname>Seggery (Mrs.) </surname>
<given-names>P.</given-names></name>
<name><surname>Stove</surname>
<given-names>E. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1917</fpage>
<lpage>1919</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001917">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001917">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Derivatives of 6-aminopenicillanic acid. Part XI. α-Amino-&lt;i&gt;p&lt;/i&gt;-hydroxy-benzylpenicillin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001920</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Long</surname>
<given-names>A. A. W.</given-names></name>
<name><surname>Nayler</surname>
<given-names>J. H. C.</given-names></name>
<name><surname>Smith</surname>
<given-names>H.</given-names></name>
<name><surname>Taylor</surname>
<given-names>T.</given-names></name>
<name><surname>Ward</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1920</fpage>
<lpage>1922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001920">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001920">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CD. Total syntheses of &lt;i&gt;NO&lt;/i&gt;(10)-dimethylhernovine and kreysigine by photolysis of diazotised isoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001923</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Koizumi</surname>
<given-names>M.</given-names></name>
<name><surname>Shishido</surname>
<given-names>K.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1923</fpage>
<lpage>1927</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001923">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001923">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CDI. Rearrangement of β-hydroxylaudanosine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001927</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Hirata</surname>
<given-names>S.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1927</fpage>
<lpage>1929</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001927">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001927">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The alkaline hydrolysis of sterically crowded phosphonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001930</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corfield</surname>
<given-names>J. R.</given-names></name>
<name><surname>De'Ath</surname>
<given-names>N. J.</given-names></name>
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1930</fpage>
<lpage>1933</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001930">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001930">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic analogues of polynucleotides. Part V. Analogues of trinucleoside diphosphates containing carboxymethylthymidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001933</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edge</surname>
<given-names>M. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1933</fpage>
<lpage>1939</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001933">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001933">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance spectra of xanthines and thioxanthines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001939</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lichtenberg</surname>
<given-names>D.</given-names></name>
<name><surname>Bergmann</surname>
<given-names>F.</given-names></name>
<name><surname>Neiman</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1939</fpage>
<lpage>1941</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001939">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001939">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XVIII. Some 6,7-diaminoimidazo[1,2-&lt;i&gt;a&lt;/i&gt;]-pyrimidines and derived tricyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001942</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Ramsden</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1942</fpage>
<lpage>1944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001942">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001942">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XIX. Some 6-(substituted phenyl)-uracil and -thiouracil derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001945</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Munawar</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1945</fpage>
<lpage>1948</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001945">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001945">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XX. The action of hydrazine on some 1,3-dimethyl-lumazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001948</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Smith</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1948</fpage>
<lpage>1951</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001948">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001948">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitroxide chemistry. Part I. Reactions of bistrifluoromethyl nitroxide with acetylene, 3,3,3-trifluoropropyne, perfluoropropyne, perfluorobut-2-yne, perfluorodiphenylacetylene, and glyoxal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001951</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Myerscough</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1951</fpage>
<lpage>1957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001951">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001951">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic polyfluoro-compounds. Part XX. Nucleophilic substitution in perfluoro-(4-phenylpyridine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001957</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Barlow</surname>
<given-names>M. G.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Phillips</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1957</fpage>
<lpage>1960</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001957">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001957">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photochemistry of ketones derived from carbohydrates. Part I. Type I cleavage of a pyranosid-4-ulose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001960</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>Peter M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1960</fpage>
<lpage>1965</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001960">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001960">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photochemistry of ketones derived from carbohydrates. Part II. Evidence for a biradical mechanism in type i ring contraction of pyranosid-4-uloses to furanosides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001965</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>Peter M.</given-names></name>
<name><surname>Gupta</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1965</fpage>
<lpage>1968</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001965">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001965">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biosynthesis of terpenes and steroids. Part V. The synthesis of ergosta-5,7,22,24(28)-tetraen-3β-ol, a biosynthetic precursor of ergosterol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001968</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Shioiri</surname>
<given-names>T.</given-names></name>
<name><surname>Widdowson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1968</fpage>
<lpage>1974</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001968">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001968">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrroles and related compounds. Part XIX. Synthesis of phylloporphyrins related to &lt;i&gt;chlorobium&lt;/i&gt; chlorophyll (660)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001974</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>M. T.</given-names></name>
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1974</fpage>
<lpage>1981</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001974">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001974">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of a new flavone, ‘arthraxin’</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001982</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Keneta</surname>
<given-names>Makoto</given-names></name>
<name><surname>Sugiyama</surname>
<given-names>Noboru</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1982</fpage>
<lpage>1986</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001982">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001982">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated compounds containing nitrogen. Part I. The synthesis and disproportionation of 1-chloro-azines, and their reactions with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001986</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>W. T.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
<name><surname>Wright</surname>
<given-names>C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1986</fpage>
<lpage>1991</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001986">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001986">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carcinogenic nitrogen compounds. Part LXX. Polycyclic naphthyridines by means of the Ullmann–Fetvadjian reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001991</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
<name><surname>Mangane</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1991</fpage>
<lpage>1993</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001991">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001991">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of the natural isoflavanones ferreirin, dalbergioidin, and ougenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710001994</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Farkas</surname>
<given-names>L.</given-names></name>
<name><surname>Gottsegen</surname>
<given-names>Á.</given-names></name>
<name><surname>Nógrádi</surname>
<given-names>M.</given-names></name>
<name><surname>Antus</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1994</fpage>
<lpage>2000</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710001994">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710001994">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naturally occurring quinones. Part XIX. Anthraquinones in &lt;i&gt;hymenodictyon excelsum&lt;/i&gt; and &lt;i&gt;damnacanthus major&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brew</surname>
<given-names>E. J. C.</given-names></name>
<name><surname>Thomason</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2001</fpage>
<lpage>2007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naturally occurring quinones. Part XX. Anthraquinones in &lt;i&gt;digitalis purpurea&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brew</surname>
<given-names>E. J. C.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2007</fpage>
<lpage>2010</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sesquitepenes. Part VI. Stereochemistry of hydroboration of some tricyclo[5,4,0,0&lt;sup&gt;3,5&lt;/sup&gt;]undecenes and related β-isopropyloctalins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fringuelli</surname>
<given-names>Francesco</given-names></name>
<name><surname>Taticchi</surname>
<given-names>Aldo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2011</fpage>
<lpage>2012</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enol elimination reactions. Part IV. Some improvements to the synthesis of conjugated acetylenic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002013</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>Ian</given-names></name>
<name><surname>Owen</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2013</fpage>
<lpage>2017</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002013">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002013">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and reactions of pyrrolo[2,1-&lt;i&gt;c&lt;/i&gt;][1,2,4]benzotriazine and 4-oxo-4&lt;i&gt;H&lt;/i&gt;-pyrrolo[2,1-&lt;i&gt;c&lt;/i&gt;][1,4]benzoxazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Rafiq</surname>
<given-names>M.</given-names></name>
<name><surname>Roy</surname>
<given-names>P. D.</given-names></name>
<name><surname>Turner</surname>
<given-names>C. J.</given-names></name>
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2018</fpage>
<lpage>2022</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of organophosphorochloridates. Part II. Reactions of steroid phosphorodichloridates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002023</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Olsson</surname>
<given-names>N. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2023</fpage>
<lpage>2027</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002023">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002023">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of organophosphorochloridates. Part III. Synthesis of &lt;i&gt;N&lt;/i&gt;-substituted pyrophosphoramides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002028</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Dewhurst</surname>
<given-names>B. B.</given-names></name>
<name><surname>Wakeford</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2028</fpage>
<lpage>2031</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Constitutents of &lt;i&gt;Withania somnifera&lt;/i&gt; Dun. Part XII. The withanolides of an indian chemotype</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirson</surname>
<given-names>I.</given-names></name>
<name><surname>Glotter</surname>
<given-names>E.</given-names></name>
<name><surname>Lavie</surname>
<given-names>D.</given-names></name>
<name><surname>Abraham</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2032</fpage>
<lpage>2044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic hydroxamic acids. Part I. Synthesis and reactions of 1,2-di-hydro-1-hydroxy-4,6-dimethyl-2-oxopyridine-3-carbonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rafla</surname>
<given-names>Fathi Kamel</given-names></name>
<name><surname>Khan</surname>
<given-names>Mazhar Ali</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2044</fpage>
<lpage>2048</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridine-2-thiones, 2-pyrone phenylhydrazones, and 2-pyridones from 2-pyrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002048</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rafla</surname>
<given-names>Fathi Kamel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2048</fpage>
<lpage>2053</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solution photodimerization of 1,3-dimethyluracil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elad</surname>
<given-names>D.</given-names></name>
<name><surname>Rosenthal</surname>
<given-names>I.</given-names></name>
<name><surname>Sasson</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2053</fpage>
<lpage>2057</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Applications of high-potential quinones. Part VI. Stereoelectronic effects in the dehydrogenation of neoergosterols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002057</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>W.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2057</fpage>
<lpage>2061</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002057">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002057">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New reactions of polyfluoroaromatic compounds. Part II. Polyfluoroaralkyl amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002062</article-id><contrib-group><contrib contrib-type="author">
<name><surname>White</surname>
<given-names>William L.</given-names></name>
<name><surname>Filler</surname>
<given-names>Robert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2062</fpage>
<lpage>2068</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002062">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002062">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclization of some Δ&lt;sup&gt;7&lt;/sup&gt;-22-hydroxy-steroids to 14β,22-ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002069</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aberhart</surname>
<given-names>D. J.</given-names></name>
<name><surname>Caspi</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2069</fpage>
<lpage>2073</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002069">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002069">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Re-examination of the reaction of β-naphthol with &lt;i&gt;trans-p&lt;/i&gt;-nitrobenzene-diazocyanide: a novel fission of the azo double bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kikuchi</surname>
<given-names>Y.</given-names></name>
<name><surname>Mitsuhashi</surname>
<given-names>T.</given-names></name>
<name><surname>Simamura</surname>
<given-names>O.</given-names></name>
<name><surname>Yoshida</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2074</fpage>
<lpage>2075</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The stereochemistry of organometallic compounds. Part X. Further evidence as to the mechanism of borohydride reduction of organomercurials from a study of photochemical and organotin hydride reductions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002075</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>V. M. A.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
<name><surname>Young</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2075</fpage>
<lpage>2079</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002075">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002075">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzopyrones. Part IV. Pyrano[1,4]benzoxazinones and some dihydrobenzoxazines: synthesis, mass, and nuclear magnetic resonance spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002079</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>G.</given-names></name>
<name><surname>Ellis</surname>
<given-names>G. P.</given-names></name>
<name><surname>Wilson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2079</fpage>
<lpage>2082</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002079">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002079">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biosynthesis of dolicotheline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002083</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horan</surname>
<given-names>H.</given-names></name>
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2083</fpage>
<lpage>2085</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation of phenazines by the cyclisation of 2-nitrodiphenylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002085</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>B.</given-names></name>
<name><surname>Williams</surname>
<given-names>P. J.</given-names></name>
<name><surname>Woodall</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2085</fpage>
<lpage>2090</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002085">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002085">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arylnaphthalene lignans: synthesis of helioxanthin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002091</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holmes</surname>
<given-names>T. L.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>Robert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2091</fpage>
<lpage>2094</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of 2-aminothiazoles and 2-aminobenzothiazoles with propiolic acid and its esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002094</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dunwell</surname>
<given-names>D. W.</given-names></name>
<name><surname>Evans</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2094</fpage>
<lpage>2097</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002094">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002094">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation of derivatives of dibenz[&lt;i&gt;b,d&lt;/i&gt;]oxepin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002098</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrow</surname>
<given-names>T. A.</given-names></name>
<name><surname>Harrison</surname>
<given-names>(Miss) C. E.</given-names></name>
<name><surname>Williamson</surname>
<given-names>W. R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2098</fpage>
<lpage>2104</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002098">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002098">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation and properties of thiophen analogues of porphyrins and related systems. Part III</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002104</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahmed</surname>
<given-names>M.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2104</fpage>
<lpage>2111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002104">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002104">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part XIII. Reaction of αβ-unsaturated acid chlorides with primary and secondary enamines. Synthesis of tetrahydro-2-oxopyridines and octahydro-2-oxoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002112</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2112</fpage>
<lpage>2115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some ring-A fused heterocycles in the lanosterol series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briggs</surname>
<given-names>Lindsay H.</given-names></name>
<name><surname>Bartley</surname>
<given-names>J. P.</given-names></name>
<name><surname>Rutledge</surname>
<given-names>P. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2115</fpage>
<lpage>2119</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;-aryl-&lt;i&gt;N&lt;/i&gt;-phenylhydroxylamines from phenylmagnesium bromide and nitro-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002119</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yost</surname>
<given-names>Yul</given-names></name>
<name><surname>Gutmann</surname>
<given-names>H. R.</given-names></name>
<name><surname>Muscoplat</surname>
<given-names>C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2119</fpage>
<lpage>2122</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002119">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002119">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical modification of trehalose. Part VIII. The synthesis of 3,3′-dideoxy-analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Richardson</surname>
<given-names>A. C.</given-names></name>
<name><surname>Tarelli</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2122</fpage>
<lpage>2127</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of terpenes. Part XIII. Synthesis of (+)-3β,7,7-trimethyl-&lt;i&gt;anti,cis,anti&lt;/i&gt;-tricyclo[4,1,0,0&lt;sup&gt;2,4&lt;/sup&gt;]heptane and (±)-&lt;i&gt;trans&lt;/i&gt;-3-(1-hydroxyethyl)-6,6-dimethylbicyclo[3,1,0]hexane, deamination products of the &lt;i&gt;cis&lt;/i&gt;-caran-4-amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002127</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyle</surname>
<given-names>P. H.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Gordon</surname>
<given-names>R. L.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2127</fpage>
<lpage>2136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002127">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002127">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of terpenes. Part XIV. Syntheses of (±)- and (+)-fenchone, and (+)-&lt;i&gt;cis&lt;/i&gt;-2,2,5-trimethyl-3-vinylcyclopentanone, a photoisomer of (–)-&lt;i&gt;trans&lt;/i&gt;-caran-4-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyle</surname>
<given-names>P. H.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Grayson</surname>
<given-names>D. H.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2136</fpage>
<lpage>2142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on heteroaromaticity. Part XLVIII. Cycloaddition reactions of 4-phenyl-1,2,4-triazoline-3,5-dione with seven-membered ring unsaturated compounds and photochemical behaviour of the adducts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sasaki</surname>
<given-names>Tadashi</given-names></name>
<name><surname>Kanematsu</surname>
<given-names>Ken</given-names></name>
<name><surname>Hayakawa</surname>
<given-names>Kenji</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2142</fpage>
<lpage>2147</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of cyanoacetylenes. Part IX. Preparation of pyrazole derivatives &lt;i&gt;via&lt;/i&gt; 1,3-dipolar cycloaddition reactions of cyanoacetylenes with diazomethane, &lt;i&gt;N&lt;/i&gt;-phenylsydnone, and diphenylnitrilimine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002147</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sasaki</surname>
<given-names>Tadashi</given-names></name>
<name><surname>Kanematsu</surname>
<given-names>Ken</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2147</fpage>
<lpage>2150</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002147">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002147">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>α-Cyano-sulphonyl chlorides: their preparation and reactions with amines, alcohols, and enamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002151</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sammes</surname>
<given-names>M. P.</given-names></name>
<name><surname>Wylie</surname>
<given-names>(Mrs.) C. M.</given-names></name>
<name><surname>Hoggett</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2151</fpage>
<lpage>2155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002151">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002151">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of polyazaheterocyclic compounds. Part V. The synthesis and reactivity of the &lt;i&gt;v&lt;/i&gt;-triazolo[3,4-&lt;i&gt;a&lt;/i&gt;]pyrimidine ring system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sutherland</surname>
<given-names>D. R.</given-names></name>
<name><surname>Tennant</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2156</fpage>
<lpage>2162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of 2-aminopyridine with some β-keto-esters in the presence of polyphosphoric acid ethyl ester</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Brown</surname>
<given-names>T. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2163</fpage>
<lpage>2164</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part I. Introduction to the series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2164</fpage>
<lpage>2166</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part II. The synthesis of potential ring a and ring C–ring D components</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002166</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Halpern</surname>
<given-names>B.</given-names></name>
<name><surname>Porter</surname>
<given-names>Q. N.</given-names></name>
<name><surname>Collins</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2166</fpage>
<lpage>2174</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002166">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002166">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part III. Michael-type cyclisation in the formation of ring B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002175</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aufderhaar</surname>
<given-names>E.</given-names></name>
<name><surname>Baldwin</surname>
<given-names>J. E.</given-names></name>
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Faulkner</surname>
<given-names>D. J.</given-names></name>
<name><surname>Slaytor</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2175</fpage>
<lpage>2183</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002175">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002175">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part IV. Ring B formation through 1,3-dipolar additions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002184</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>J. E.</given-names></name>
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Gutteridge</surname>
<given-names>N. J. A.</given-names></name>
<name><surname>Martin</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2184</fpage>
<lpage>2192</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002184">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002184">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments of the synthesis of tetracycline. Part V. Photocyclisation of ring B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002193</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Clive</surname>
<given-names>D. L. J.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
<name><surname>Smith</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2193</fpage>
<lpage>2203</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002193">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002193">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part VI. Oxidation and reduction of potential ring A precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002204</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Bould</surname>
<given-names>L.</given-names></name>
<name><surname>Clive</surname>
<given-names>D. L. J.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
<name><surname>Hase</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2204</fpage>
<lpage>2215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002204">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002204">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part VII. The total synthesis of 6-methylpretetramid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002215</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
<name><surname>Hase</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2215</fpage>
<lpage>2225</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002215">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002215">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part VIII. An attempted total synthesis of 4-hydroxy-6-methylpretetramid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
<name><surname>Pearson</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2225</fpage>
<lpage>2231</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part IX. The synthesis and rearrangement of 6-acyloxycyclohexa-2,4-dienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002231</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
<name><surname>Pearson</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2231</fpage>
<lpage>2241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002231">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002231">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the synthesis of tetracycline. Part X. Synthesis of a tetracyclic compound suitable for 12aα-hydroxylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Challis</surname>
<given-names>(Mrs.) J. A.</given-names></name>
<name><surname>Magnus</surname>
<given-names>P. D.</given-names></name>
<name><surname>Marshall</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2241</fpage>
<lpage>2243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Light-induced and related reactions of quinones. Part VII. Cleavage and isomerisation of some (1-hydroxyalkyl)-1,4-benzoquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002244</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bruce</surname>
<given-names>J. Malcolm</given-names></name>
<name><surname>Creed</surname>
<given-names>David</given-names></name>
<name><surname>Dawes</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2244</fpage>
<lpage>2252</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002244">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002244">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>4-Amino-2,3,4,5-tetrahydro-1-benzoxepin-5-ols, 4-amino-2,3,4,5-tetrahydro-1-benzothiepin-5-ols, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002252</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huckle</surname>
<given-names>D.</given-names></name>
<name><surname>Lockhart</surname>
<given-names>I. M.</given-names></name>
<name><surname>Webb</surname>
<given-names>N. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2252</fpage>
<lpage>2260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002252">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002252">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metabolic products of &lt;i&gt;Stemphylium radicinum&lt;/i&gt;. Part IV. Minor products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grove</surname>
<given-names>John Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2261</fpage>
<lpage>2263</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reversible isomerisation of alkyl aromatics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Osman</surname>
<given-names>A. M.</given-names></name>
<name><surname>Badr</surname>
<given-names>M. Z. A.</given-names></name>
<name><surname>Abdel-Rahman</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2264</fpage>
<lpage>2265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of lead tetra-acetate with substituted benzothiazolylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>R. N.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>P.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2265</fpage>
<lpage>2268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diels–Alder reactions with alkyl coumalates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002268</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bahl</surname>
<given-names>A. K.</given-names></name>
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2268</fpage>
<lpage>2271</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>One-electron transfer properties of diquaternary salts of 2-(2-pyridyl)-quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002271</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Black</surname>
<given-names>A. L.</given-names></name>
<name><surname>Summers</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2271</fpage>
<lpage>2273</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002271">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002271">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The effect of chloro-substituents on the rate of nitrogen inversion in 1-phthalimidoaziridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002273</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. J.</given-names></name>
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2273</fpage>
<lpage>2274</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002273">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002273">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrophenylcarbenes. Part I. The catalytic and photolytic decomposition of α-diazo-3-nitrotoluene in the presence of olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goh</surname>
<given-names>S. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2275</fpage>
<lpage>2278</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XXI. Synthesis and covalent hydration of some 2-substituted 4-trifluoromethylpteridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002278</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Yates</surname>
<given-names>F. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2278</fpage>
<lpage>2282</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002278">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002278">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The induced decomposition of t-butyl peroxide in solution. Part III. Decomposition of t-butyl peroxide in alkyl benzyl ethers; steric effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goh</surname>
<given-names>S. H.</given-names></name>
<name><surname>Huang</surname>
<given-names>R. L.</given-names></name>
<name><surname>Ong</surname>
<given-names>S. H.</given-names></name>
<name><surname>Sieh</surname>
<given-names>Iling</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2282</fpage>
<lpage>2286</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structures and thermal rearrangements of alkylated palladium and copper corroles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002287</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Shelton</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2287</fpage>
<lpage>2294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002287">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002287">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkylated steroids from tosylhydrazones and alkyl-lithiums</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002294</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Herz</surname>
<given-names>Josef E.</given-names></name>
<name><surname>Ortiz</surname>
<given-names>Ciria Valencia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2294</fpage>
<lpage>2295</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002294">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002294">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel analgesics and molecular rearrangements in the morphine–thebaine group. Part XXI. Alcohols derived from 7-methyl-&lt;i&gt;epi&lt;/i&gt;-nepenthone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002296</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>J. W.</given-names></name>
<name><surname>Readhead</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2296</fpage>
<lpage>2298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002296">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002296">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel analgesics and molecular rearrangements in the morphine–thebaine group. Part XXII. Deamination of 7β-aminomethyl-6,14-&lt;i&gt;endo&lt;/i&gt;-etheno-7α-methyl-6,7,8,14-tetrahydrothebaine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002298</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>J. W.</given-names></name>
<name><surname>Readhead</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2298</fpage>
<lpage>2300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydroxy-steroids. Part XVII. The 5α-androstane-16,17-diols and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002300</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Combe</surname>
<given-names>(Miss) M. G.</given-names></name>
<name><surname>Denny</surname>
<given-names>W. A.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Morisawa</surname>
<given-names>Y.</given-names></name>
<name><surname>Richards</surname>
<given-names>(Mrs.) E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2300</fpage>
<lpage>2305</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002300">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002300">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part XIX. The reaction of methyl 6-deoxy-3-&lt;i&gt;O&lt;/i&gt;-methyl-4-&lt;i&gt;O&lt;/i&gt;-methylsulphonyl-2-&lt;i&gt;O&lt;/i&gt;-&lt;i&gt;p&lt;/i&gt;-tolylsulphonyl-α-D-allopyranoside with sodium benzoate in hexamethylphosphoric triamide: a vicinal axial substituent effect</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Radhi</surname>
<given-names>A. K.</given-names></name>
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Tucker</surname>
<given-names>L. C. N.</given-names></name>
<name><surname>Ching</surname>
<given-names>O. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2305</fpage>
<lpage>2308</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carcinogenic nitrogen compounds. Part LXXI. Acridines from 5-aminobenzo[&lt;i&gt;b&lt;/i&gt;]selenophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002308</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Dufour</surname>
<given-names>M.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
<name><surname>Renson</surname>
<given-names>M.</given-names></name>
<name><surname>Maréchal</surname>
<given-names>G.</given-names></name>
<name><surname>Ruwet</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2308</fpage>
<lpage>2310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The action of sodium sulphide on 1,3,4-oxadiazolium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Summers</surname>
<given-names>A. J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2311</fpage>
<lpage>2313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The dimerisation of 5-methylene-Δ&lt;sup&gt;2&lt;/sup&gt;-1,3,4-oxadiazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Dando</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2314</fpage>
<lpage>2317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triazines and related products. Part VIII. Potential irreversible chymotrypsin inhibitors: 3-alkyl-1,2,3-benzotriazin-4(3&lt;i&gt;H&lt;/i&gt;)-ones and &lt;i&gt;o&lt;/i&gt;-azidobenzamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mair</surname>
<given-names>A. C.</given-names></name>
<name><surname>Stevens</surname>
<given-names>M. F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2317</fpage>
<lpage>2324</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A probe for homolytic reactions in solution. Part V. Perdeuterionitrosobutane: an improved spin trap</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002324</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holman</surname>
<given-names>R. J.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2324</fpage>
<lpage>2326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002324">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002324">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of the isomers of the mono- and di-hydroxy-analogues of cystine and comparison with metabolites excreted in the urine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002326</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wälti</surname>
<given-names>M.</given-names></name>
<name><surname>Hope</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2326</fpage>
<lpage>2328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002326">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002326">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Friedel–Crafts acylations of aromatic hydrocarbons. Part X. Benzoylation of phenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Thadani</surname>
<given-names>C. K.</given-names></name>
<name><surname>Thorburn</surname>
<given-names>S.</given-names></name>
<name><surname>Yusuf</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2329</fpage>
<lpage>2330</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of &lt;i&gt;O&lt;/i&gt;-methylation. Some factors affecting the ratio of glycosides produced in the methylation of L-rhamnose derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haines</surname>
<given-names>A. H.</given-names></name>
<name><surname>Symes</surname>
<given-names>K. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2331</fpage>
<lpage>2334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Keten. Part XI. The addition of dimethylketen to &lt;i&gt;N&lt;/i&gt;-(2,6-xylyl)benzylideneamine &lt;i&gt;N&lt;/i&gt;-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stokes</surname>
<given-names>D. P.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2334</fpage>
<lpage>2336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The hydrolysis of arylmethylenemalononitriles to α-cyanocinnamides in the presence of triphenylphosphine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002336</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Powell</surname>
<given-names>R. L.</given-names></name>
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2336</fpage>
<lpage>2338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002336">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002336">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Asymmetric syntheses. Part V. The absolute configuration of some acetylenic alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Miller</surname>
<given-names>B. J.</given-names></name>
<name><surname>Tatchell</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2339</fpage>
<lpage>2341</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosensitised oxidation of amines. Part I. The use of benzophenone as a sensitiser</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002342</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartholomew</surname>
<given-names>R. F.</given-names></name>
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2342</fpage>
<lpage>2346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002342">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002342">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosensitised oxidation of amines. Part II. The use of dyes as photosensitisers: evidence that singlet oxygen is not involved</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartholomew</surname>
<given-names>R. F.</given-names></name>
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2347</fpage>
<lpage>2351</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002347">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part XII. (&lt;i&gt;S&lt;/i&gt;)-3-ethynyl-4-methylcyclohex-3-en-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002352</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawson</surname>
<given-names>T. M.</given-names></name>
<name><surname>Dixon</surname>
<given-names>J.</given-names></name>
<name><surname>Littlewood</surname>
<given-names>P. S.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2352</fpage>
<lpage>2355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002352">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002352">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidation of olefins by manganese(III) acetate to give allylic acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilmore</surname>
<given-names>J. R.</given-names></name>
<name><surname>Mellor</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2355</fpage>
<lpage>2357</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XL. The synthesis of 4-unsubstituted pteridines from 3-aminopyrazine-2-carbaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002357</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Aderien</given-names></name>
<name><surname>Ohta</surname>
<given-names>Kyuji</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2357</fpage>
<lpage>2362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002357">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002357">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Friedel–Crafts acylation of aromatic halogen derivatives. Part V. The reaction of aluminium chloride with iodobenzene and the iodotoluenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002362</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Thorburn</surname>
<given-names>S.</given-names></name>
<name><surname>Weyell</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2362</fpage>
<lpage>2364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002362">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002362">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 3-methylisoguanine [6-amino-3-methylpurin-2(3&lt;i&gt;H&lt;/i&gt;)-one]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogers</surname>
<given-names>G. T.</given-names></name>
<name><surname>Ulbricht</surname>
<given-names>T. L. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2364</fpage>
<lpage>2366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002364">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free-radical reactions of halogenated bridged polycyclic compounds. Part XIV. The cobalt(II) chloride-catalysed reaction of methylmagnesium iodide with 5-&lt;i&gt;endo&lt;/i&gt;-bromo-1,2,3,4,7,7-hexachloronorborn-2-ene and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002367</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alexander</surname>
<given-names>Richard</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Done</surname>
<given-names>J. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2367</fpage>
<lpage>2371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002367">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002367">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some steroidal &lt;i&gt;p&lt;/i&gt;-aminophenyl ethers and their &lt;i&gt;N&lt;/i&gt;-methyl and &lt;i&gt;NN&lt;/i&gt;-dimethyl analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002372</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>D. D.</given-names></name>
<name><surname>Weyell</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2372</fpage>
<lpage>2373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002372">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002372">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The stobbe condensation of 3,4-disubstituted acetophenones with diethyl succinate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>El-Newaihy</surname>
<given-names>M. F.</given-names></name>
<name><surname>El-Hashash</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2373</fpage>
<lpage>2375</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2-Isoxazoline derivatives. Part IV. Bromination of some dihydro-acenaphtho[1,2-&lt;i&gt;d&lt;/i&gt;]isoxazole derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bianchi</surname>
<given-names>G.</given-names></name>
<name><surname>Gamba</surname>
<given-names>A.</given-names></name>
<name><surname>Gandolfi</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2375</fpage>
<lpage>2381</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 1-iodo- and 1,2-di-iodo-perfluorocyclo-olefins and reductive coupling of the latter in the presence of copper bronze</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002382</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Camaggi</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2382</fpage>
<lpage>2388</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002382">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some derivatives of &lt;i&gt;NN&lt;/i&gt;′-biscarboxymethyl- and &lt;i&gt;NN&lt;/i&gt;′-bis-(β-carboxyethyl)-ethylenediamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002389</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haydock</surname>
<given-names>D. B.</given-names></name>
<name><surname>Mulholland</surname>
<given-names>T. P. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2389</fpage>
<lpage>2395</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002389">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002389">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A total synthesis of (±)-capaurimine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002396</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Honda</surname>
<given-names>T.</given-names></name>
<name><surname>Ihara</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2396</fpage>
<lpage>2398</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002396">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002396">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The biosynthesis of pilocereine. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002398</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Barry</surname>
<given-names>E.</given-names></name>
<name><surname>Horan</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2398</fpage>
<lpage>2399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002398">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002398">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tropylidene quinones and their tricarbonylchromium complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002399</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
<name><surname>Watson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2399</fpage>
<lpage>2403</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002399">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002399">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated nitrogen compounds containing fluorine. Part I. The thermal and photochemical reactions of hexafluoroacetone azine with acetylene and with hydrocarbon terminal olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forshaw</surname>
<given-names>T. P.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2404</fpage>
<lpage>2408</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction by dissolving metals. Part XVII. Metal–ammonia reductions of some conjugated dienamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002409</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hutchinson</surname>
<given-names>E. G.</given-names></name>
<name><surname>Rao</surname>
<given-names>G. Subba</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2409</fpage>
<lpage>2411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002409">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002409">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of hop constituents. Part XXXVII. Separation and characterisation of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-isohumulone and deduction of absolute configurations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002412</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laws</surname>
<given-names>D. R. J.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2412</fpage>
<lpage>2415</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002412">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002412">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The significant directing effect of the cyano-group in the reduction of 5-cyano-3-oxo-steroids with complex metal hydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002415</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nagata</surname>
<given-names>W.</given-names></name>
<name><surname>Wakabayashi</surname>
<given-names>T.</given-names></name>
<name><surname>Narisada</surname>
<given-names>M.</given-names></name>
<name><surname>Hayase</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2415</fpage>
<lpage>2420</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002415">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002415">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure and stereochemistry of gangetin, a new pterocarpan from &lt;i&gt;Desmodium gangeticum&lt;/i&gt;(Leguminosae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Purushothaman</surname>
<given-names>K. K.</given-names></name>
<name><surname>Kishore</surname>
<given-names>V. M.</given-names></name>
<name><surname>Narayanaswami</surname>
<given-names>V.</given-names></name>
<name><surname>Connolly</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2420</fpage>
<lpage>2422</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rearrangement of 1α,2-epoxy-3-oxo-5α-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002422</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tortorella</surname>
<given-names>V.</given-names></name>
<name><surname>Toscano</surname>
<given-names>L.</given-names></name>
<name><surname>Vetuschi</surname>
<given-names>C.</given-names></name>
<name><surname>Romeo</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2422</fpage>
<lpage>2423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002422">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002422">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some stereospecific reactions of dibromides from &lt;i&gt;o&lt;/i&gt;-cyanocinnamonitriles and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002424</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. E. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2424</fpage>
<lpage>2427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002424">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002424">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thiophen derivatives. Part XXI. New nitrogen-containing heterocyclic systems from 5-aminobenzo[&lt;i&gt;b&lt;/i&gt;]thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Dufour</surname>
<given-names>M.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
<name><surname>Martani</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2428</fpage>
<lpage>2430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A convenient synthesis of &lt;i&gt;cis&lt;/i&gt;-bicyclo[3,3,0]octane-1-carboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002430</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McKervey</surname>
<given-names>M. A.</given-names></name>
<name><surname>Quinn</surname>
<given-names>H. A.</given-names></name>
<name><surname>Rooney</surname>
<given-names>J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2430</fpage>
<lpage>2431</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002430">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002430">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Two new mould metabolites related to avenaciolide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aldridge</surname>
<given-names>D. C.</given-names></name>
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2431</fpage>
<lpage>2432</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and reduction of optically active 2-mercaptopropionic acid and some derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002432</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
<name><surname>Rahman</surname>
<given-names>M. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2432</fpage>
<lpage>2440</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002432">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002432">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrazolopyrimidine nucleosides. Part I. Synthesis of pyrazolopyrimidine nucleosides related to the nucleoside antibiotic tubercidin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002440</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Revankar</surname>
<given-names>Ganapthi R.</given-names></name>
<name><surname>Townsend</surname>
<given-names>Leroy B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2440</fpage>
<lpage>2442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002440">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002440">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrazolopyrimidine nucleosides. Part II. 7-Substituted 3-β-D-ribofuranosylpyrazolo[4,3-&lt;i&gt;d&lt;/i&gt;]pyrimidines related to and derived from the nucleoside antibiotics formycin and formycin B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Long</surname>
<given-names>Robert A.</given-names></name>
<name><surname>Lewis</surname>
<given-names>Arthur F.</given-names></name>
<name><surname>Robins</surname>
<given-names>Roland K.</given-names></name>
<name><surname>Townsend</surname>
<given-names>Leroy B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2443</fpage>
<lpage>2446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on total photolytic syntheses of alkaloids. Part V. Total syntheses of flavinantine, amurine, bracteoline, and domesticine by photolysis of the appropriate 1-(2-bromobenzyl)isoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Sugi</surname>
<given-names>H.</given-names></name>
<name><surname>Kusama</surname>
<given-names>O.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2446</fpage>
<lpage>2448</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of pyrido[1,2-&lt;i&gt;b&lt;/i&gt;][2,4]benzodiazepin-6(11&lt;i&gt;H&lt;/i&gt;)-one and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002449</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>M.</given-names></name>
<name><surname>Knowles</surname>
<given-names>P.</given-names></name>
<name><surname>Sharp</surname>
<given-names>B. W.</given-names></name>
<name><surname>Walsh</surname>
<given-names>R. J. A.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2449</fpage>
<lpage>2451</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002449">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002449">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic organophosphorus compounds. Part XII. Use of 2-benzoyloxy-5,5-dimethyl-2-oxo-1,3,2-dioxaphosphorinan under steric control in acylations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Forth</surname>
<given-names>C. I.</given-names></name>
<name><surname>Moran</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2452</fpage>
<lpage>2453</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organolithium chemistry of &lt;i&gt;N&lt;/i&gt;-heterocycles. Part III. Reduction of 2-methylquinoline by lithium in tetrahydrofuran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002453</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>A. M.</given-names></name>
<name><surname>Russell</surname>
<given-names>C. A.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2453</fpage>
<lpage>2457</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002453">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002453">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Resolution and thermal racemisation of nickel 1,19-dimethyltetradehydrocorrin salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002457</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. P.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Smith</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2457</fpage>
<lpage>2461</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002457">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002457">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal structure of a cyclopentenylidenephosphorane isolated from the reaction of tri-&lt;i&gt;p&lt;/i&gt;-tolylphosphine and dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002461</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kennard</surname>
<given-names>Olga</given-names></name>
<name><surname>Motherwell</surname>
<given-names>W. D. S.</given-names></name>
<name><surname>Coppola</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2461</fpage>
<lpage>2464</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002461">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002461">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organometallic complexes in synthesis. Part III. The reaction of concentrated sulphuric acid with tricarbonylcyclohexa-1,3-dieneiron complexes: a preparation of certain alkyltricarbonyl-π-cyclohexadienyliron salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002465</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Haas</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2465</fpage>
<lpage>2467</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002465">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002465">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on lactams. Part XIV. The synthesis of a structural isomer of penicillin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002468</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bose</surname>
<given-names>Ajay K.</given-names></name>
<name><surname>Spiegelman</surname>
<given-names>G.</given-names></name>
<name><surname>Manhas</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2468</fpage>
<lpage>2472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002468">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002468">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses of 3-(2,4-dimethyl-5-oxocyclopent-1-enyl)propionic acid and 2-methyl-3-oxo-4-isopropylidenecyclopentanecarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002472</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Narayanan</surname>
<given-names>K. V.</given-names></name>
<name><surname>Balasubramianian</surname>
<given-names>K. K.</given-names></name>
<name><surname>Chandrasekaran</surname>
<given-names>S.</given-names></name>
<name><surname>Ramani</surname>
<given-names>S.</given-names></name>
<name><surname>Swaminathan</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2472</fpage>
<lpage>2474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002472">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002472">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic studies. Part XXIII. 5-Trifluoromethylpyrimido[5,4-&lt;i&gt;e&lt;/i&gt;]-&lt;i&gt;as&lt;/i&gt;-triazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002475</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Yates</surname>
<given-names>F. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2475</fpage>
<lpage>2479</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl azide with 2,3-dimethylindole, 1,2,3-trimethylindole, tetrahydrocarbazole, and 9-methyltetrahydrocarbazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002479</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Scattergood</surname>
<given-names>R.</given-names></name>
<name><surname>Warr</surname>
<given-names>(Mrs.) W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2479</fpage>
<lpage>2491</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002479">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002479">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Seco-steroids. Part I. 15,16-Secoprogesterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002491</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crossley</surname>
<given-names>N. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2491</fpage>
<lpage>2495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002491">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002491">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Seco-steroids. Part II. 9,11-Secoprogesterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002496</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crossley</surname>
<given-names>N. S.</given-names></name>
<name><surname>Dowell</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2496</fpage>
<lpage>2498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002496">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002496">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Seco-steroids. Part III. 5,6-Secoprogesterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crossley</surname>
<given-names>N. S.</given-names></name>
<name><surname>Dowell</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2499</fpage>
<lpage>2502</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part XVII. Orientation of the nitrogen lone pairs in &lt;i&gt;trans&lt;/i&gt;-decahydroquinazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002502</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Kobayashi</surname>
<given-names>Toshihiko</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2502</fpage>
<lpage>2504</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002502">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002502">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Condensed thiophen ring systems. Part VI. Synthesis and some reactions of 5-methyl- and 5-chloro-3-benzo[&lt;i&gt;b&lt;/i&gt;]thienyl-lithium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002504</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dickinson</surname>
<given-names>R. P.</given-names></name>
<name><surname>Iddon</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2504</fpage>
<lpage>2506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002504">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002504">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The dimroth rearrangement. Part XIV. The preparation and rearrangement of 1,6-dihydro-6-imino-1-methylpyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>England</surname>
<given-names>B. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2507</fpage>
<lpage>2512</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction between aromatic compounds and derivatives of tertiary acids. Part XI II. The structure of phenylcamphoric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002512</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bantick</surname>
<given-names>John R.</given-names></name>
<name><surname>Rothstein</surname>
<given-names>Eugene</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2512</fpage>
<lpage>2521</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002512">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002512">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Raman spectra and frequency calculations for some steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002521</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beattie</surname>
<given-names>I. R.</given-names></name>
<name><surname>Hudec</surname>
<given-names>J.</given-names></name>
<name><surname>Livingston</surname>
<given-names>K. M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2521</fpage>
<lpage>2525</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002521">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002521">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of triterpenes and related compounds. Part XLVII. Crystal and molecular structure of ‘compound B’, a triterpene dimethyl ester ɛ-lactone from dammar resin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002525</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>H. R.</given-names></name>
<name><surname>Hodder</surname>
<given-names>O. J. R.</given-names></name>
<name><surname>Brewis</surname>
<given-names>S.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2525</fpage>
<lpage>2529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002525">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002525">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal structure of the diterpene tinophyllone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brehm</surname>
<given-names>L.</given-names></name>
<name><surname>Hodder</surname>
<given-names>O. J. R.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2529</fpage>
<lpage>2534</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Epoxides of some pyrazolylprop-2-en-1-ones and their reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002534</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
<name><surname>Mahmud</surname>
<given-names>S. Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2534</fpage>
<lpage>2536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002534">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002534">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and ultraviolet and nuclear magnetic resonance spectra of some 9-substituted 9,10-dihydroacridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002537</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>G. A.</given-names></name>
<name><surname>Procter</surname>
<given-names>S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2537</fpage>
<lpage>2538</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002537">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002537">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chlorination of indole alkaloids and related compounds with 1-chlorobenzotriazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002539</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lichman</surname>
<given-names>K. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2539</fpage>
<lpage>2540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002539">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002539">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CDVIII. Crystal structure of capaurimine mono-&lt;i&gt;p&lt;/i&gt;-bromobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002541</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Ihara</surname>
<given-names>M.</given-names></name>
<name><surname>Honda</surname>
<given-names>T.</given-names></name>
<name><surname>Shimanouchi</surname>
<given-names>H.</given-names></name>
<name><surname>Sasada</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2541</fpage>
<lpage>2545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002541">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002541">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A new 2-phenyl-4&lt;i&gt;H&lt;/i&gt;-1-benzopyran (flav-2-ene) synthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002546</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casiraghi</surname>
<given-names>G.</given-names></name>
<name><surname>Casnati</surname>
<given-names>G.</given-names></name>
<name><surname>Salerno</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2546</fpage>
<lpage>2548</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002546">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002546">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The pyrethrins and related compounds. Part XI. Synthesis of insecticidal esters of 4-hydroxycyclopent-2-enones (nor-rethrins)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002548</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elliott</surname>
<given-names>M.</given-names></name>
<name><surname>Janes</surname>
<given-names>N. F.</given-names></name>
<name><surname>Payne</surname>
<given-names>Mrs. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2548</fpage>
<lpage>2551</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002548">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002548">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The pyrethrins and related compounds. Part XII. 5-Substituted 3-furoates and 3-thenoates, intermediates for synthesis of insecticidal esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002551</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elliott</surname>
<given-names>M.</given-names></name>
<name><surname>Janes</surname>
<given-names>N. F.</given-names></name>
<name><surname>Pearson</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2551</fpage>
<lpage>2554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002551">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002551">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic heteroaromatic substitution. Derivatives of pyrrolo-[2,1-&lt;i&gt;b&lt;/i&gt;]oxazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Vecchietti</surname>
<given-names>V.</given-names></name>
<name><surname>Dradi</surname>
<given-names>E.</given-names></name>
<name><surname>Lauria</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2554</fpage>
<lpage>2557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lithium alkyl(hydro)dipinan-3α-ylborates. New reagents for asymmetric reduction of ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002557</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grundon</surname>
<given-names>M. F.</given-names></name>
<name><surname>Khan</surname>
<given-names>W. A.</given-names></name>
<name><surname>Boyd</surname>
<given-names>D. R.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2557</fpage>
<lpage>2559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002557">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002557">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Asymmetric reduction of imines with lithium butyl(hydro)dipinan-3α-yl-borate and related reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002560</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Archer</surname>
<given-names>J. F.</given-names></name>
<name><surname>Boyd</surname>
<given-names>D. R.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
<name><surname>Grundon</surname>
<given-names>M. F.</given-names></name>
<name><surname>Khan</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2560</fpage>
<lpage>2563</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroid conjugates. Part IV. The influence of the cation in borohydride reduction of ketol sulphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002563</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxendale</surname>
<given-names>D.</given-names></name>
<name><surname>Kirk</surname>
<given-names>D. N.</given-names></name>
<name><surname>Rajagopalan</surname>
<given-names>M. S.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2563</fpage>
<lpage>2566</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002563">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002563">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Applications of high-potential quinones. Part VII. The synthesis of steroidal phenanthrenes by double methyl migration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002566</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>W.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2566</fpage>
<lpage>2572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002566">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002566">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photochemical conversion of some heterocyclic acraldehydes into derivatives of propionic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002572</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>L. S.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2572</fpage>
<lpage>2576</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of mononitropyrogallols and their methyl ethers, acetates, and benzenesulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kampouris</surname>
<given-names>Emmanuel M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2577</fpage>
<lpage>2579</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and deamination of cyclohex-1-enyl- and cyclohexa-1,4-dienyl-methylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002580</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stapleford</surname>
<given-names>K. S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2580</fpage>
<lpage>2582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002580">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002580">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Constituents of the higher fungi. Part XI. Boviquinone-3, (2,5-dihydroxy-3-farnesyl-1,4-benzoquinone), diboviquinone-3,4, methylenediboviquinone-3,3, and xerocomic acid from &lt;i&gt;Gomphidius rutilus&lt;/i&gt; Fr. and diboviquinone-4,4 from &lt;i&gt;Boletus&lt;/i&gt;(&lt;i&gt;Suillus&lt;/i&gt;)&lt;i&gt;bovinus&lt;/i&gt;(Linn ex Fr.) Kuntze</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002582</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaumont</surname>
<given-names>P. C.</given-names></name>
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2582</fpage>
<lpage>2585</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002582">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002582">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Friedel–Crafts acylations of aromatic hydrocarbons. Part XI. The acetylation and benzoylation of 2,6-dimethylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002586</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Yusuf</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2586</fpage>
<lpage>2590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002586">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002586">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acid-catalysed reactions of &lt;i&gt;N&lt;/i&gt;-(diphenylmethylene)methylthiomethyl-amine &lt;i&gt;N&lt;/i&gt;-oxide and &lt;i&gt;O&lt;/i&gt;-(methylthiomethyl)benzophenone oxime</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002591</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>I. W.</given-names></name>
<name><surname>Kerr</surname>
<given-names>D. A.</given-names></name>
<name><surname>Wilson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2591</fpage>
<lpage>2595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002591">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002591">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal reactions of &lt;i&gt;N&lt;/i&gt;-(diphenylmethylene)methylthiomethylamine &lt;i&gt;N&lt;/i&gt;-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002595</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>I. W.</given-names></name>
<name><surname>Kerr</surname>
<given-names>D. A.</given-names></name>
<name><surname>Wilson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2595</fpage>
<lpage>2598</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of leucogenenol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002599</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rice</surname>
<given-names>F. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2599</fpage>
<lpage>2606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002599">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002599">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carcinogenic nitrogen compounds. Part LXXII. The Möhlau–Bischler reaction as a preparative route to 2-arylindoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002606</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Saint-Ruf</surname>
<given-names>G.</given-names></name>
<name><surname>Deschamps</surname>
<given-names>D.</given-names></name>
<name><surname>Hieu</surname>
<given-names>H.-T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2606</fpage>
<lpage>2609</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002606">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002606">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and stereochemistry of Δ&lt;sup&gt;2,2′&lt;/sup&gt;-bi-(2&lt;i&gt;H&lt;/i&gt;-1,4-benzothiazine) derivatives. Crystal structures of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-Δ&lt;sup&gt;2,2′&lt;/sup&gt;-bi-(3-&lt;i&gt;p&lt;/i&gt;-bromophenyl-2&lt;i&gt;H&lt;/i&gt;-1,4-benzothiazine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002610</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Giordano</surname>
<given-names>F.</given-names></name>
<name><surname>Mazzarella</surname>
<given-names>L.</given-names></name>
<name><surname>Prota</surname>
<given-names>G.</given-names></name>
<name><surname>Santacroce</surname>
<given-names>C.</given-names></name>
<name><surname>Sica</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2610</fpage>
<lpage>2616</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002610">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002610">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aza-analogues of pteridine. Part IV. The transformation of 7-chloro-1,2-dihydro- into 5,7-disubstituted-pyrimido[5,4-&lt;i&gt;e&lt;/i&gt;]-&lt;i&gt;as&lt;/i&gt;-triazines &lt;i&gt;via&lt;/i&gt; 5,6-adducts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002616</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Sugimoto</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2616</fpage>
<lpage>2620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002616">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002616">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction of nitro- and nitroso-compounds by tervalent phosphorus reagents. Part IX. The ‘blocked &lt;i&gt;ortho&lt;/i&gt;’ effect in reactions of 2,6-di-substituted aryl 2-nitrophenyl and 2,6-disubstituted aryl 2-azidophenyl sulphides: a new series of nitrene-induced aromatic rearrangements</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Kulik</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2621</fpage>
<lpage>2632</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenolic cyclisation. Part X. Isoquinoline cyclisation under basic conditions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002632</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Ishimaru</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2632</fpage>
<lpage>2634</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002632">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002632">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2-Azafluoranthene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002634</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birnie</surname>
<given-names>J. M.</given-names></name>
<name><surname>Campbell</surname>
<given-names>Neil</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2634</fpage>
<lpage>2637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002634">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002634">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 1,1-diarylethylenes with selenium compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002637</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elmaleh</surname>
<given-names>D.</given-names></name>
<name><surname>Patai</surname>
<given-names>S.</given-names></name>
<name><surname>Rappoport</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2637</fpage>
<lpage>2640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002637">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002637">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Observations on the conversion of acetone into pinacol hydrate by magnesium amalgam</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002641</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Binks</surname>
<given-names>J.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2641</fpage>
<lpage>2644</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002641">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002641">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on heterocyclic chemistry. Part VIII. Comparison of the thermally induced reaction of 4-substituted 5-aminoisoxazoles with the decomposition of isoxazoles by arylamine, with reference to a 2&lt;i&gt;H&lt;/i&gt;-azirine intermediate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002644</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishiwaki</surname>
<given-names>Tarozaemon</given-names></name>
<name><surname>Saito</surname>
<given-names>Toshinori</given-names></name>
<name><surname>Onomura</surname>
<given-names>Satoko</given-names></name>
<name><surname>Kondo</surname>
<given-names>Koichi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2644</fpage>
<lpage>2647</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002644">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002644">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on heterocyclic chemistry. Part IX. Reaction of 2-(carbonyl)-2&lt;i&gt;H&lt;/i&gt;-azirines with hydrazine. A novel and unequivocal synthesis of 1,2,4-triazin-6-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002648</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishiwaki</surname>
<given-names>Tarozaemon</given-names></name>
<name><surname>Saito</surname>
<given-names>Toshinori</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2648</fpage>
<lpage>2652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homogeneous catalysis by transition-metal complexes. Part II. An investigation of the hydrogen-transfer reaction catalysed by the henbest system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gullotti</surname>
<given-names>M.</given-names></name>
<name><surname>Ugo</surname>
<given-names>R.</given-names></name>
<name><surname>Colonna</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2652</fpage>
<lpage>2656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation of nucleoside carbonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002656</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tittensor</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2656</fpage>
<lpage>2662</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002656">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002656">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triterpenoids from &lt;i&gt;Entandrophragma cylindricum&lt;/i&gt; sprague. Part II. The structures of sapelins C, D, E, and F</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002662</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Yee</surname>
<given-names>T. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2662</fpage>
<lpage>2667</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002662">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002662">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Autoxidation of polysubstituted isoindoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kricka</surname>
<given-names>L. J.</given-names></name>
<name><surname>Vernon</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2667</fpage>
<lpage>2670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bicyclo[4,3,0]nonanes (hydrindanes). Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002671</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baggaley</surname>
<given-names>K. H.</given-names></name>
<name><surname>Brooks</surname>
<given-names>S. G.</given-names></name>
<name><surname>Green</surname>
<given-names>J.</given-names></name>
<name><surname>Redman</surname>
<given-names>B. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2671</fpage>
<lpage>2678</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002671">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002671">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bicyclo[4,3,0]nonanes (hydrindanes). Part II. Stability relationships</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002678</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baggaley</surname>
<given-names>K. H.</given-names></name>
<name><surname>Brooks</surname>
<given-names>S. G.</given-names></name>
<name><surname>Green</surname>
<given-names>J.</given-names></name>
<name><surname>Redman</surname>
<given-names>B. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2678</fpage>
<lpage>2680</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002678">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002678">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homolytic aromatic substitution. Part XXXVI. Total and partial rate factors for the phenylation of some &lt;i&gt;para&lt;/i&gt;-disubstituted derivatives of benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002681</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Summers</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2681</fpage>
<lpage>2684</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002681">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002681">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Approaches to heterocyclic analogues of biphenylene. Part I. The reaction of 5,6-diaryl-2,3-dihydropyrazines with alcoholic alkali</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002685</article-id><contrib-group><contrib contrib-type="author">
<name><surname>England</surname>
<given-names>P.</given-names></name>
<name><surname>McDougall</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2685</fpage>
<lpage>2689</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002685">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002685">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of oligosaccharides on polymer supports. Part I. 6-&lt;i&gt;O&lt;/i&gt;-(&lt;i&gt;p&lt;/i&gt;-vinylbenzoyl) derivatives of glucopyranose and their copolymers with styrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002690</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
<name><surname>Jenkins</surname>
<given-names>A. D.</given-names></name>
<name><surname>Stehlícek</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2690</fpage>
<lpage>2696</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002690">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002690">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acetylation and acetoxylation of 4-hydroxy-1,4-benzothiazin- and -benzoxazin-3(4&lt;i&gt;H&lt;/i&gt;)-ones (cyclic hydroxamic acids)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002696</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coutts</surname>
<given-names>R. T.</given-names></name>
<name><surname>Pound</surname>
<given-names>N. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2696</fpage>
<lpage>2699</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002696">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002696">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions with aldehydes of enaminones derived from dimedone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002699</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greenhill</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2699</fpage>
<lpage>2703</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002699">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002699">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The biosynthesis of sclerin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002703</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tokoroyama</surname>
<given-names>T.</given-names></name>
<name><surname>Kubota</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2703</fpage>
<lpage>2708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002703">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002703">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CDXII. Total synthesis of canadine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002709</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Terui</surname>
<given-names>T.</given-names></name>
<name><surname>Yamaki</surname>
<given-names>K.</given-names></name>
<name><surname>Taguchi</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2709</fpage>
<lpage>2711</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002709">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzyne reaction. Part XII. Syntheses of amurine and domesticine by the benzyne reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Kusama</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2712</fpage>
<lpage>2714</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of carbonyl compounds with tervalent phosphorus reagents. Part I. Cyclopentadienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002714</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>J. A.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>G. M.</given-names></name>
<name><surname>Williams</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2714</fpage>
<lpage>2720</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002714">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002714">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of acetonedicarboxylic anhydride (tetrahydropyrantrione) and its mono- and di-acetyl derivatives with amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiang</surname>
<given-names>A. K.</given-names></name>
<name><surname>Tan</surname>
<given-names>S. F.</given-names></name>
<name><surname>Wong</surname>
<given-names>W. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2721</fpage>
<lpage>2726</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002721">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and uses of a poly(allyl carbonate)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>S. A.</given-names></name>
<name><surname>Kennedy</surname>
<given-names>J. F.</given-names></name>
<name><surname>Rosevear</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2726</fpage>
<lpage>2730</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002726">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A convenient preparation of cyclohexane-1,4-dicarbaldehyde and cyclohexane-1,1,4,4-tetramethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002730</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beam</surname>
<given-names>Charles F.</given-names></name>
<name><surname>Bailey</surname>
<given-names>William J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2730</fpage>
<lpage>2731</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002730">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002730">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Further cyclisation reactions of 1-arylpyrroles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002732</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Rafiq</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2732</fpage>
<lpage>2734</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002732">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002732">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quaternary salts of pyrido[1,2-&lt;i&gt;a&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002735</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landquist</surname>
<given-names>Justus K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2735</fpage>
<lpage>2738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002735">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002735">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The acid thermal decomposition products of natural chrysanthemumdicarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Doherty</surname>
<given-names>Christine F.</given-names></name>
<name><surname>Pattenden</surname>
<given-names>Gerald</given-names></name>
<name><surname>Woods</surname>
<given-names>D. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2739</fpage>
<lpage>2743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002739">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroalkyl derivatives of nitrogen. Part XXIX. Reaction of &lt;i&gt;N&lt;/i&gt;-bromobistrifluoromethylamine with &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-but-2-ene and of &lt;i&gt;N&lt;/i&gt;-chlorobistrifluoromethylamine with &lt;i&gt;trans&lt;/i&gt;-but-2-ene under ionic conditions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002744</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlow</surname>
<given-names>M. G.</given-names></name>
<name><surname>Fleming</surname>
<given-names>G. L.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2744</fpage>
<lpage>2747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002744">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002744">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic quaternary ammonium salts. Part VIII. Imidazo[1,2-&lt;i&gt;a&lt;/i&gt;]pyrazinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002748</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adamson</surname>
<given-names>J.</given-names></name>
<name><surname>Glover</surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2748</fpage>
<lpage>2749</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002748">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002748">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluorocarbanion chemistry. Part I. Reaction of hexafluoropropene with tetrafluoropyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002750</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drayton</surname>
<given-names>C. J.</given-names></name>
<name><surname>Flowers</surname>
<given-names>W. T.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2750</fpage>
<lpage>2755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002750">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002750">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of pyridine &lt;i&gt;N&lt;/i&gt;-oxides with 3,6-dichloropyridazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deegan</surname>
<given-names>A.</given-names></name>
<name><surname>Rose</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2756</fpage>
<lpage>2763</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformational free energy differences in steroids. Part VI. Intramolecular electrostatic interactions in 3-azidocholestan-6-ones: conformational preference of the azido-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002763</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. Neville</given-names></name>
<name><surname>Wyse</surname>
<given-names>K. J.</given-names></name>
<name><surname>Kime</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2763</fpage>
<lpage>2769</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002763">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002763">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conversion of tetrazolyl hydrazones into triazolyl azides &lt;i&gt;via&lt;/i&gt; tetrazolyl hydrazidic halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002769</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Cronin</surname>
<given-names>D. A.</given-names></name>
<name><surname>O'Halloran</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2769</fpage>
<lpage>2775</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002769">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002769">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chlorination of carbazole and its derivatives with 1-chlorobenzotriazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002775</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowyer</surname>
<given-names>P. M.</given-names></name>
<name><surname>Iles</surname>
<given-names>D. H.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2775</fpage>
<lpage>2777</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002775">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002775">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitroxide chemistry. Part II. Reaction of bistrifluoromethyl nitroxide with some alkanes and alkenes; free-radical dehydrogenation of alkanes to alkenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002777</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Justin</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2777</fpage>
<lpage>2785</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002777">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002777">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isolation and characterization of a fungal vacuolation factor (bikaverin)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002786</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cornforth</surname>
<given-names>J. W.</given-names></name>
<name><surname>Ryback</surname>
<given-names>G.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. M.</given-names></name>
<name><surname>Park</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2786</fpage>
<lpage>2788</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002786">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002786">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of the chloroform solvate of bikaverin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002788</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boer</surname>
<given-names>J. J. de</given-names></name>
<name><surname>Bright</surname>
<given-names>D.</given-names></name>
<name><surname>Dallinga</surname>
<given-names>G.</given-names></name>
<name><surname>Hewitt</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2788</fpage>
<lpage>2791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002788">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002788">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bikaverin and norbikaverin, benzoxanthentrione pigments of &lt;i&gt;Gibberella fujikuroi&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002792</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kjær</surname>
<given-names>D.</given-names></name>
<name><surname>Kjær</surname>
<given-names>A.</given-names></name>
<name><surname>Pedersen</surname>
<given-names>C.</given-names></name>
<name><surname>Bu'Lock</surname>
<given-names>J. D.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2792</fpage>
<lpage>2797</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002792">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002792">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Antituberculosis agents. Part II. α-[5-(2-Furyl)-1,3,4-oxadiazol-2-yl-thio]acetohydrazide and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002798</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mir</surname>
<given-names>I.</given-names></name>
<name><surname>Siddiqui</surname>
<given-names>M. T.</given-names></name>
<name><surname>Comrie</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2798</fpage>
<lpage>2799</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002798">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002798">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of cyclo-octatetraene and its derivatives. Part III. Cycloocta-1,3,5-triene as a dienophile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002800</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akhtar</surname>
<given-names>I. A.</given-names></name>
<name><surname>Fray</surname>
<given-names>G. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2800</fpage>
<lpage>2802</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002800">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002800">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Highly condensed polycyclic systems. Part III. Pentacyclo-[5,5,1,0&lt;sup&gt;2,6&lt;/sup&gt;,0&lt;sup&gt;3,10&lt;/sup&gt;,0&lt;sup&gt;4,8&lt;/sup&gt;]tridec-11-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002802</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akhtar</surname>
<given-names>I. A.</given-names></name>
<name><surname>Fray</surname>
<given-names>G. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2802</fpage>
<lpage>2804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002802">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002802">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosensitised oxidation of amines. Part III. The use of xanthone, fluorenone, &lt;i&gt;p&lt;/i&gt;-aminobenzophenone, and methyl β-naphthyl ketone as sensitisers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartholomew</surname>
<given-names>R. F.</given-names></name>
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Howell</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2804</fpage>
<lpage>2806</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3,4,5-Triphenylpyrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002807</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Comrie</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2807</fpage>
<lpage>2810</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002807">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002807">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction products from &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-isocohumulone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002810</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Byrne</surname>
<given-names>E.</given-names></name>
<name><surname>Shaw</surname>
<given-names>S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2810</fpage>
<lpage>2813</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002810">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002810">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part XIII. Syntheses of two fourteen-membered ring cyclotetrapeptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Sanger</surname>
<given-names>D. G.</given-names></name>
<name><surname>Handa</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2814</fpage>
<lpage>2818</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Shikimate pathway. Part III. The stereochemical course of the L-phenylalanine ammonia lyase reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ife</surname>
<given-names>R.</given-names></name>
<name><surname>Haslam</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2818</fpage>
<lpage>2821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An improved synthesis of substituted benzoyl acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002821</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckle</surname>
<given-names>D. R.</given-names></name>
<name><surname>Smith</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2821</fpage>
<lpage>2823</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002821">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002821">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and photochemistry of 2,2′-distyrylbiphenyl and 2,2′-bis-(4-phenylbuta-1,3-dienyl)biphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002824</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tulloch</surname>
<given-names>C. D.</given-names></name>
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2824</fpage>
<lpage>2826</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002824">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002824">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structures of three C&lt;sub&gt;32&lt;/sub&gt; triterpenoids from &lt;i&gt;Neolitsea pulchella&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002826</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hui (Miss) </surname>
<given-names>W. H.</given-names></name>
<name><surname>Luk</surname>
<given-names>K.</given-names></name>
<name><surname>Arthur</surname>
<given-names>(the late) H. R.</given-names></name>
<name><surname>Loo</surname>
<given-names>S. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2826</fpage>
<lpage>2829</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002826">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002826">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of heterocyclic compounds. Part IX. Formylation of 6a-thiathiophthens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002829</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duguay</surname>
<given-names>G.</given-names></name>
<name><surname>Reid</surname>
<given-names>D. H.</given-names></name>
<name><surname>Wade</surname>
<given-names>K. O.</given-names></name>
<name><surname>Webster</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2829</fpage>
<lpage>2833</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002829">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002829">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenol oxidation. The formation of benzofuran and 2,3-dihydrobenzofuran derivatives by oxidation of 1-(2-hydroxyphenyl)-2-(4-hydroxyphenyl)ethanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002834</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Ward</surname>
<given-names>R. S.</given-names></name>
<name><surname>Choudhury</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2834</fpage>
<lpage>2837</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002834">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002834">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure and synthesis of a tetrahydro-β-carboline alkaloid from &lt;i&gt;Phalaris arundinacea&lt;/i&gt;: some new tetrahydro-β-carbolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002837</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
<name><surname>Leyshon</surname>
<given-names>W. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2837</fpage>
<lpage>2839</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002837">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002837">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The sulphur(II)–nitrogen bond. Part I. Reaction of alkanesulphenyl chlorides with secondary amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002840</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armitage</surname>
<given-names>D. A.</given-names></name>
<name><surname>Clark</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2840</fpage>
<lpage>2842</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002840">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002840">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2,3-Benzothiadiazoles. Part III. Nucleophilic substitution reactions in halogeno-1,2,3-benzothiadiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002843</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>J. H.</given-names></name>
<name><surname>Haddock</surname>
<given-names>E.</given-names></name>
<name><surname>Kirby</surname>
<given-names>P.</given-names></name>
<name><surname>Webb</surname>
<given-names>Shirley B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2843</fpage>
<lpage>2846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002843">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002843">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6β-Bromoacetoxy-, 6β-chloroacetoxy-, and 6β-iodoacetoxy-3,5α-cyclo-5α-cholestane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002846</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2846</fpage>
<lpage>2846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002846">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002846">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton magnetic resonance spectra of some &lt;i&gt;para&lt;/i&gt;-substituted derivatives of 9-phenylazojulolidine (9-phenylazo-2,3,6,7-tetrahydro-1&lt;i&gt;H&lt;/i&gt;,5&lt;i&gt;H&lt;/i&gt;-benzo[&lt;i&gt;ij&lt;/i&gt;]quinolizine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002847</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2847</fpage>
<lpage>2848</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002847">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002847">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The algar–flynn–oyamada oxidation of α-substituted chalcones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002848</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cullen</surname>
<given-names>W. P.</given-names></name>
<name><surname>Donnelly</surname>
<given-names>D. M. X.</given-names></name>
<name><surname>Keenan</surname>
<given-names>A. K.</given-names></name>
<name><surname>Lavin</surname>
<given-names>T. P.</given-names></name>
<name><surname>Melody</surname>
<given-names>D. P.</given-names></name>
<name><surname>Philbin</surname>
<given-names>E. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2848</fpage>
<lpage>2855</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002848">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002848">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Total synthesis of polymethoxyoestrane compounds. Part I. Synthesis of (±)-2,3,4-trimethoxyoestra-1,3,5(10)-trien-17β-ol and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rao</surname>
<given-names>P. Narasimha</given-names></name>
<name><surname>Jacob</surname>
<given-names>E. John</given-names></name>
<name><surname>Axelrod</surname>
<given-names>Leonard R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2855</fpage>
<lpage>2860</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Total synthesis of polymethoxyoestrane compounds. Part II. Synthesis of (±)-2,4-dimethoxyoestra-1,3,5(10)-trien-17β-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002861</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rao</surname>
<given-names>P. Narasimha</given-names></name>
<name><surname>Axelrod</surname>
<given-names>Leonard R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2861</fpage>
<lpage>2863</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002861">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002861">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis of vicinal trimethoxyoctahydrophenanthrene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002863</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rao</surname>
<given-names>P. Narasimha</given-names></name>
<name><surname>Edwards</surname>
<given-names>Ben E.</given-names></name>
<name><surname>Axelrod</surname>
<given-names>Leonard R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2863</fpage>
<lpage>2865</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002863">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002863">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Light-induced rearrangement of aryloxyacetonitriles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002865</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arora</surname>
<given-names>K. J. S.</given-names></name>
<name><surname>Dirania</surname>
<given-names>M. K. M.</given-names></name>
<name><surname>Hill</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2865</fpage>
<lpage>2866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002865">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002865">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogeno-aromatic compounds. Part XXI. A novel reagent system for the &lt;i&gt;N&lt;/i&gt;-oxidation of weakly basic &lt;i&gt;N&lt;/i&gt;-heteroaromatic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002867</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chivers</surname>
<given-names>G. E.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2867</fpage>
<lpage>2871</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002867">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002867">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mechanism of the reaction between trialkyl phosphites and halogenoacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002872</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burt</surname>
<given-names>D. W.</given-names></name>
<name><surname>Simpson</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2872</fpage>
<lpage>2876</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002872">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002872">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The gentamicin antibiotics. Part II. Separation and degradation of the gentamicin C components. The purpurosamines, a new class of naturally occurring 2,6-diaminomonosaccharides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002876</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>David J.</given-names></name>
<name><surname>Yudis</surname>
<given-names>Milton D.</given-names></name>
<name><surname>Marigliano</surname>
<given-names>Henrietta M.</given-names></name>
<name><surname>Traubel</surname>
<given-names>Theodor</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2876</fpage>
<lpage>2879</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002876">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002876">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the reaction of benzoyl peroxide with &lt;i&gt;NN&lt;/i&gt;-disubstituted aromatic amines and related compounds. Part V. Preparation of 5,11-disubstituted 5,6,11,12-tetrahydrophenhomazines from α-diamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002880</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2880</fpage>
<lpage>2888</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002880">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002880">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The potential-controlled anodic oxidation of 1,2-dimethoxy-4-prop-1-enylbenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002888</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sainsbury</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2888</fpage>
<lpage>2889</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002888">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002888">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The biosynthesis of &lt;i&gt;Lobelia&lt;/i&gt; alkaloids. Part II. The role of lobelanine in the biosynthesis of lobeline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Forde</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2889</fpage>
<lpage>2890</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amino-acids and peptides. Part XXXIV. Anchimerically assisted coupling reactions: the use of 2-pyridyl thiolesters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002890</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lloyd</surname>
<given-names>K.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2890</fpage>
<lpage>2896</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002890">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002890">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polypeptides. Part XII. The preparation of 2-pyridyl esters and their use in peptide synthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002896</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dutta</surname>
<given-names>A. S.</given-names></name>
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2896</fpage>
<lpage>2902</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002896">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002896">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Terpenoids. Part XVIII. A common stereoelectronic requirement in epimerisations and retro-Dieckmann-type cleavages of some diterpene alcohols and ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002902</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fujita</surname>
<given-names>E.</given-names></name>
<name><surname>Nagao</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2902</fpage>
<lpage>2907</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002902">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002902">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Branched-chain sugars. Part XIII. Synthesis of 4′-&lt;i&gt;O&lt;/i&gt;-methylapiin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002907</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ezekiel</surname>
<given-names>A. D.</given-names></name>
<name><surname>Overend</surname>
<given-names>W. G.</given-names></name>
<name><surname>Williams</surname>
<given-names>N. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2907</fpage>
<lpage>2911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002907">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002907">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A synthesis of 2-&lt;i&gt;O&lt;/i&gt;-methyl-L-lyxose, a component of everninomicins B and D</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002911</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Mofti</surname>
<given-names>A. M.</given-names></name>
<name><surname>Tucker</surname>
<given-names>L. C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2911</fpage>
<lpage>2915</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002911">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002911">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of &lt;i&gt;exo&lt;/i&gt;- and &lt;i&gt;endo&lt;/i&gt;-bicyclo[3,2,1]octane-2-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002915</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cantello</surname>
<given-names>B. C. C.</given-names></name>
<name><surname>Mellor</surname>
<given-names>J. M.</given-names></name>
<name><surname>Scholes</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2915</fpage>
<lpage>2919</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002915">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002915">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclisations &lt;i&gt;via&lt;/i&gt; fluoride ion induced isomerisations: a route to some novel perfluoroheterocyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002920</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ogden</surname>
<given-names>Paul H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2920</fpage>
<lpage>2926</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002920">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002920">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic compounds from urea derivatives. Part XX. Adducts from carbonohydrazides and aroyl isothiocyanates and their cyclisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002927</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2927</fpage>
<lpage>2931</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002927">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002927">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic compounds from urea derivatives. Part XXI. Adducts from thiocarbonohydrazides and aroyl isothiocyanates and their cyclisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002932</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2932</fpage>
<lpage>2938</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002932">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002932">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermolysis of diazotetraphenylcyclopentadiene in the presence of amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002939</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
<name><surname>Singer</surname>
<given-names>M. I. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2939</fpage>
<lpage>2940</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002939">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002939">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation of 2,3,4-triphenylcyclopentadienylides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002941</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
<name><surname>Singer</surname>
<given-names>M. I. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2941</fpage>
<lpage>2944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part XIII. Derivatives of enantiomeric 4-methylcyclohex-3-ene-1,&lt;i&gt;trans&lt;/i&gt;-2-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002944</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>I. J.</given-names></name>
<name><surname>Harrison</surname>
<given-names>R. G.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
<name><surname>Manwaring</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2944</fpage>
<lpage>2949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002944">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002944">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part XIV. Total synthesis of des-AB-cholestane-8β,9α-diol &lt;sup&gt;2&lt;/sup&gt;{1β-[(1&lt;i&gt;R&lt;/i&gt;)-1,5-dimethylhexyl]-7aβ-methyl-&lt;i&gt;trans&lt;/i&gt;-perhydroindane-4β,5α-diol}</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002950</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>I. J.</given-names></name>
<name><surname>Harrison</surname>
<given-names>R. G.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2950</fpage>
<lpage>2955</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002950">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002950">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part XV. The preparation of des-AB-cholest-8-ene-8-carbaldehyde {1β-[(1&lt;i&gt;R&lt;/i&gt;)-1,5-dimethylhexyl]-3aα,6,7,7aβ-tetrahydro-7aβ-methylindane-4-carbaldehyde} and 9α-chloro-des-AB-cholestan-8-one {5α-chloro-1β-[(1&lt;i&gt;R&lt;/i&gt;)-1,5-dimethylhexyl]-7aβ-methyl-&lt;i&gt;trans&lt;/i&gt;-perhydroindan-4-one}</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002955</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Littlewood</surname>
<given-names>P. S.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
<name><surname>Saksena</surname>
<given-names>A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2955</fpage>
<lpage>2959</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002955">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002955">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calciferol and its relatives. Part XVI. Total synthesis of precalciferol&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;2&lt;/sup&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002960</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawson</surname>
<given-names>T. M.</given-names></name>
<name><surname>Dixon</surname>
<given-names>J.</given-names></name>
<name><surname>Littlewood</surname>
<given-names>P. S.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
<name><surname>Saksena</surname>
<given-names>A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2960</fpage>
<lpage>2966</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002960">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002960">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The copper–amine catalysed autoxidation of phenols. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002967</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewitt</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2967</fpage>
<lpage>2973</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002967">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002967">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrazines. Part III. Some nucleophilic substitution reactions of chloropyrazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002973</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Godwin</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2973</fpage>
<lpage>2976</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002973">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002973">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrazines. Part IV. 2,6-Dihydroxy-3,5-diphenylpyrazine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002977</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Godwin</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2977</fpage>
<lpage>2979</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002977">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002977">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New metabolites of &lt;i&gt;Gibberella fujikuroi&lt;/i&gt;. Part XVIII. 4bβ,7-Dihydroxy-1-methyl-8-methylenegibba-1,3,4a(10a)-trien-10-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002980</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>B. E.</given-names></name>
<name><surname>Markwell</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2980</fpage>
<lpage>2983</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002980">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002980">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituted aminoacetamides by reaction of glyoxal with secondary amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002984</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferruti</surname>
<given-names>Paolo</given-names></name>
<name><surname>Feré</surname>
<given-names>Angelino</given-names></name>
<name><surname>Zetta</surname>
<given-names>Lucia</given-names></name>
<name><surname>Bettelli</surname>
<given-names>Alberto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2984</fpage>
<lpage>2985</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002984">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002984">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naphthyridines. Part III. Preparation of pyrimido[1,2-&lt;i&gt;a&lt;/i&gt;]- and imidazo-[1,2-&lt;i&gt;a&lt;/i&gt;]-[1,8]naphthyridines from 2-amino-1,8-naphthyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002985</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harper</surname>
<given-names>J. F.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2985</fpage>
<lpage>2991</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002985">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002985">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naphthyridines. Part IV. Preparation of anthyridines and pyrimido-[4,5-&lt;i&gt;b&lt;/i&gt;][1,8]naphthyridines from 2-amino-1,8-naphthyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002991</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harper</surname>
<given-names>J. F.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2991</fpage>
<lpage>2994</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002991">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002991">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transfer RNA components. Part II. Reactions of heavy metal salts of 2-thiouracil and a synthesis of 2-thiouridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002995</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogers</surname>
<given-names>G. T.</given-names></name>
<name><surname>Ulbricht</surname>
<given-names>T. L. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2995</fpage>
<lpage>2999</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002995">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002995">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Catalysed isomerisation reactions of cyclododeca-1,5,9-triene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710002999</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Attridge</surname>
<given-names>C. J.</given-names></name>
<name><surname>Maddock</surname>
<given-names>Susan J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2999</fpage>
<lpage>3001</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710002999">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710002999">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and acid-catalysed rearrangements of 4-hydroxycyclohexa-2,5-dienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003002</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burkinshaw</surname>
<given-names>(the late) G. F.</given-names></name>
<name><surname>Davis</surname>
<given-names>B. R.</given-names></name>
<name><surname>Hutchinson</surname>
<given-names>E. G.</given-names></name>
<name><surname>Woodgate</surname>
<given-names>P. D.</given-names></name>
<name><surname>Hodges</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3002</fpage>
<lpage>3006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003002">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003002">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of carbonyl compounds with tervalent phosphorus reagents. Part II. Alkyl benzoates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McNeilly</surname>
<given-names>S. T.</given-names></name>
<name><surname>Miller</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3007</fpage>
<lpage>3010</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of organophosphorochloridates. Part IV. Synthesis of &lt;i&gt;N&lt;/i&gt;-substituted phosphoramidic hydrazides, hydrazones, and azides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Dewhurst</surname>
<given-names>B. B.</given-names></name>
<name><surname>Wakeford</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3011</fpage>
<lpage>3017</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivity of vinyl sulphonic esters. Part VIII. Evidence for sulphur participation in the cyclisation of 2-arylthio-1,2-diphenylvinyl &lt;i&gt;p&lt;/i&gt;-bromobenzenesulphonates from carbon-14 labelling experiments</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capozzi</surname>
<given-names>G.</given-names></name>
<name><surname>Melloni</surname>
<given-names>G.</given-names></name>
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3018</fpage>
<lpage>3020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on heterocyclic chemistry. Part X. Synthesis of aziridin-2-ylphosphonates by the thermally induced isomerization of isoxazoles in trialkyl phosphites. A related reaction of 2&lt;i&gt;H&lt;/i&gt;-azirine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003021</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishiwaki</surname>
<given-names>Tarozaemon</given-names></name>
<name><surname>Saito</surname>
<given-names>Toshinori</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3021</fpage>
<lpage>3026</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003021">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003021">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on heterocyclic chemistry. Part XI. Synthesis of 2,3-diaryl-3-hydroxyaminoaziridine-2-carboxamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishiwaki</surname>
<given-names>Tarozaemon</given-names></name>
<name><surname>Onomura</surname>
<given-names>Satoko</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3026</fpage>
<lpage>3027</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction between 2,2-diarylchromens and 1,1-diarylethylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003028</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>E.</given-names></name>
<name><surname>Cotterill</surname>
<given-names>W. D.</given-names></name>
<name><surname>Livingstone</surname>
<given-names>R.</given-names></name>
<name><surname>Walshaw</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3028</fpage>
<lpage>3031</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organophosphorus chemistry. Part XII. Reactions of tetramethylbiphosphine and tetrakis(trifluoromethyl)biphosphine with olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003031</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>P.</given-names></name>
<name><surname>Fields</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3031</fpage>
<lpage>3035</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003031">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003031">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive intermediates. Part XV. Thermolysis of 1-(3,4-dihydro-4-oxoquinazolin-3-yl)-2-vinylaziridines. A new vinylaziridine rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
<name><surname>Stanton</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3036</fpage>
<lpage>3040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of capreomycidine and epicapreomycidine, the epimers of α-(2-iminohexahydropyrimid-4-yl)glycine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bycroft</surname>
<given-names>B. W.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3040</fpage>
<lpage>3047</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An efficient preparation of isocodeine from codeine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
<name><surname>Massey</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3047</fpage>
<lpage>3048</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of antihistaminics: dehydration of some substituted 4-aminobutan-2-ols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003048</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ison</surname>
<given-names>R. R.</given-names></name>
<name><surname>Casy</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3048</fpage>
<lpage>3051</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substitution reactions of benzo[&lt;i&gt;b&lt;/i&gt;]thiophen derivatives. Part II. Nitration and bromination of 2-bromo-3-methylbenzo[&lt;i&gt;b&lt;/i&gt;]thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003052</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>J.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3052</fpage>
<lpage>3055</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003052">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003052">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of cyanoacetylenes. Part X. Further studies on the reactions of cyano-ynamines with hydrogen halides and bromine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003056</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sasaki</surname>
<given-names>Tadashi</given-names></name>
<name><surname>Kojima</surname>
<given-names>Atsuyuki</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3056</fpage>
<lpage>3060</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003056">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003056">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amine oxidation. Part V. Reactions of some &lt;i&gt;N&lt;/i&gt;-oxides, including heterocyclic-ring formation, with sulphur dioxide, acetic anhydride, and trifluoroacetic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003060</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bather</surname>
<given-names>P. A.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. R. Lindsay</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3060</fpage>
<lpage>3068</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003060">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003060">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2,3-Dihydro-3,6-dihydroxy-2-methyl-4-pyrone and curvularin from &lt;i&gt;Penicillium gilmanii&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003069</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Raistrick</surname>
<given-names>(the late) H.</given-names></name>
<name><surname>Rice</surname>
<given-names>F. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3069</fpage>
<lpage>3070</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003069">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003069">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical constituents of the combretaceae. Part I. Substituted phenanthrenes and 9,10-dihydrophenanthrenes from the heartwood of &lt;i&gt;Combretum apiculatum&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003070</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Letcher</surname>
<given-names>R. M.</given-names></name>
<name><surname>Nhamo</surname>
<given-names>L. R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3070</fpage>
<lpage>3076</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003070">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003070">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>4-Methyl-1-phenylpentane-1,3-dione and 2-isopropylchromone from the essential oil of &lt;i&gt;Lophomyrtus bullata&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003077</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briggs</surname>
<given-names>Lindsay H.</given-names></name>
<name><surname>White</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3077</fpage>
<lpage>3079</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003077">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003077">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pharmacologically active 4-oxo-4&lt;i&gt;H&lt;/i&gt;-chromen-2-carboxylic acids. Part III. Mechanistic aspects of the decomposition of ethyl 6-azido-4-oxo-4&lt;i&gt;H&lt;/i&gt;-chromen-2-carboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003079</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chohan</surname>
<given-names>M. I.</given-names></name>
<name><surname>Fitton</surname>
<given-names>A. O.</given-names></name>
<name><surname>Hatton</surname>
<given-names>B. T.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3079</fpage>
<lpage>3081</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003079">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003079">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis of compounds containing an &lt;i&gt;o&lt;/i&gt;-nitroarylthio-substituent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003081</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goudie</surname>
<given-names>R. S.</given-names></name>
<name><surname>Preston</surname>
<given-names>P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3081</fpage>
<lpage>3084</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003081">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003081">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Claisen rearrangements of tropolone ethers. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>R. M.</given-names></name>
<name><surname>Hobson</surname>
<given-names>J. D.</given-names></name>
<name><surname>Holly</surname>
<given-names>M. M. Al</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3084</fpage>
<lpage>3087</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cinnolines. Part XV. Methylation of methoxy- and alkyl-cinnolines and -4(1&lt;i&gt;H&lt;/i&gt;)-cinnolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003088</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Ansari</surname>
<given-names>H. R.</given-names></name>
<name><surname>France</surname>
<given-names>A. D. G.</given-names></name>
<name><surname>Lovesey</surname>
<given-names>A. C.</given-names></name>
<name><surname>Novitt</surname>
<given-names>B.</given-names></name>
<name><surname>Simpson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3088</fpage>
<lpage>3097</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated compounds containing nitrogen. Part II. The preparation and thermal rearrangement of 1,4-diphenyl-1-thiocyanato-2,3-diazabuta-1,3-diene (α-thiocyanatobenzylidenehydrazonotoluene) and related reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003097</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>W. T.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
<name><surname>Wright</surname>
<given-names>C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3097</fpage>
<lpage>3099</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003097">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003097">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of 1,1-diarylethylenes with tellurium halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003100</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elmaleh</surname>
<given-names>David</given-names></name>
<name><surname>Patai</surname>
<given-names>Saul</given-names></name>
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3100</fpage>
<lpage>3108</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003100">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003100">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triterpenoid constituents of &lt;i&gt;Lycopodium phlegmaria&lt;/i&gt; L</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003109</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Inubushi</surname>
<given-names>Y.</given-names></name>
<name><surname>Hibino</surname>
<given-names>T.</given-names></name>
<name><surname>Harayama</surname>
<given-names>T.</given-names></name>
<name><surname>Hasegawa</surname>
<given-names>T.</given-names></name>
<name><surname>Somanathan</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3109</fpage>
<lpage>3114</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003109">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003109">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel tricarbonyldieneiron complexes from the reaction of 2-bromobuta-1,3-diene with carbonylirons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greene</surname>
<given-names>R. N.</given-names></name>
<name><surname>DePuy</surname>
<given-names>C. H.</given-names></name>
<name><surname>Schroer</surname>
<given-names>T. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3115</fpage>
<lpage>3120</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation of 2-amino-5,5-dimethyl-Δ&lt;sup&gt;1&lt;/sup&gt;-pyrroline 1-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003121</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gutteridge</surname>
<given-names>N. J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3121</fpage>
<lpage>3125</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003121">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003121">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The gentamicin antibiotics. Part III. The gross structures of the gentamicin C components</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003126</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Copper</surname>
<given-names>David J.</given-names></name>
<name><surname>Daniels</surname>
<given-names>Peter J. L.</given-names></name>
<name><surname>Yudis</surname>
<given-names>Milton D.</given-names></name>
<name><surname>Marigliano</surname>
<given-names>Henrietta M.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
<name><surname>Bukhari</surname>
<given-names>(Miss) S. T. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3126</fpage>
<lpage>3129</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003126">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003126">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryne chemistry. Part XXIX. Reactions of tetrahalogenobenzynes with bicyclo[2,2,1]heptene and bicyclo[2,2,1]heptadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003129</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
<name><surname>Jablonski</surname>
<given-names>J. M.</given-names></name>
<name><surname>Mason</surname>
<given-names>K. G.</given-names></name>
<name><surname>Sketchley</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3129</fpage>
<lpage>3131</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003129">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003129">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of iodonium nitrate with some olefinic alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003131</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Diner</surname>
<given-names>U. E.</given-names></name>
<name><surname>Worsley</surname>
<given-names>M.</given-names></name>
<name><surname>Lown</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3131</fpage>
<lpage>3136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactivity and the role of β-aryl-α-oxoglutaric acids in the oxidation of leucodrin and its derivatives by periodate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Perold</surname>
<given-names>G. W.</given-names></name>
<name><surname>Howard</surname>
<given-names>A. S.</given-names></name>
<name><surname>Hundt</surname>
<given-names>H. K. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3136</fpage>
<lpage>3140</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The sulphur(II)–nitrogen bond. Part II. The transamination of diamino sulphides and sulphenamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003141</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armitage</surname>
<given-names>D. A.</given-names></name>
<name><surname>Clark</surname>
<given-names>M. J.</given-names></name>
<name><surname>White</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3141</fpage>
<lpage>3142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003141">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003141">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and proton magnetic resonance spectra of the methyl ethers of 1,6-anhydro-β-D-glucopyranose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003143</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wollwage</surname>
<given-names>Paul C.</given-names></name>
<name><surname>Seib</surname>
<given-names>Paul A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3143</fpage>
<lpage>3155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003143">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003143">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Further observations on the rearrangement of 3-acylaminoazetidinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003155</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bird</surname>
<given-names>C. W.</given-names></name>
<name><surname>Twibell</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3155</fpage>
<lpage>3158</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003155">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003155">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Action of base on non-enolisable carbonyl compounds. Part II. Cleavage of some anthraquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003158</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. G.</given-names></name>
<name><surname>Hodge</surname>
<given-names>Philip</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3158</fpage>
<lpage>3164</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003158">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003158">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and reactions of triphenylarsonium cyclopentadienylide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Freeman</surname>
<given-names>Brian H.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3164</fpage>
<lpage>3165</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3,5-Diphenyloxazolidin-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003166</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irwin</surname>
<given-names>W. J.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3166</fpage>
<lpage>3167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003166">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003166">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and cyclisation of α-substituted β-(phenylthio)cinnamic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003168</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buggle</surname>
<given-names>K.</given-names></name>
<name><surname>Delahunty</surname>
<given-names>J. J.</given-names></name>
<name><surname>Philbin</surname>
<given-names>E. M.</given-names></name>
<name><surname>Ryan</surname>
<given-names>N. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3168</fpage>
<lpage>3170</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003168">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003168">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Stobbe condensation. Part VIII. The cyclisation of &lt;i&gt;trans&lt;/i&gt;-3-methoxycarbonyl-4-(2-thienyl)but-3-enoic acid and αβ-dithenylidene-succinic anhydride to the corresponding benzothiophen derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003171</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abdel-Wahhab</surname>
<given-names>(Mrs) S. M.</given-names></name>
<name><surname>El-Rayyes</surname>
<given-names>N. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3171</fpage>
<lpage>3173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The protoadamantane route to 1,2- and 2,4-disubstituted adamantanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cuddy</surname>
<given-names>B. D.</given-names></name>
<name><surname>Grant</surname>
<given-names>D.</given-names></name>
<name><surname>McKervey</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3173</fpage>
<lpage>3179</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic organophosphorus compounds. Part XIII. Stereospecific formation of 4-substituted 1,3,2-dioxaphosph(V)orinans from bicyclic phosphorus(III) esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003179</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Mitchell</surname>
<given-names>E. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3179</fpage>
<lpage>3182</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003179">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003179">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The cyclisation of 4-phenoxybutyric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lockhart</surname>
<given-names>I. M.</given-names></name>
<name><surname>Wright</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3182</fpage>
<lpage>3183</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic analogues of polynucleotides. Part VII. Further syntheses of 5′-&lt;i&gt;O&lt;/i&gt;-acryloylnucleosides and copolymers of these with other acryloyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003183</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>M. J.</given-names></name>
<name><surname>Goody</surname>
<given-names>R. S.</given-names></name>
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Tittensor</surname>
<given-names>J. R.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3183</fpage>
<lpage>3187</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003183">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003183">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of heterocyclic compounds. Part X. 6a-Selenathiophthens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003187</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Reid</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3187</fpage>
<lpage>3190</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003187">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003187">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arylsulphamoyl azides. An improved synthesis of chlorosulphonyl azide and its reaction with arylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003191</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3191</fpage>
<lpage>3195</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003191">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003191">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of indanones. Part I. The ring closure of 2-(4-methoxyphenyl)-3-(3-methoxyphenyl)propionic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003195</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. W.</given-names></name>
<name><surname>Denman</surname>
<given-names>C.</given-names></name>
<name><surname>O'Donnell</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3195</fpage>
<lpage>3198</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003195">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003195">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and fragmentation reactions of cyclic azo-compounds. Stereochemistry and transformations of photo-derived bicyclo[2,1,0]-pentanes, and thermal cycloreversion reactions of tricyclo[6,2,1,0&lt;sup&gt;2,7&lt;/sup&gt;]-undecatrienes and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003199</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lay</surname>
<given-names>W. P.</given-names></name>
<name><surname>Mackenzie</surname>
<given-names>K.</given-names></name>
<name><surname>Telford</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3199</fpage>
<lpage>3213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003199">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003199">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anodic oxidation of phenolic compounds. Part II. Products and mechanism of the anodic oxidation of hindered phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003214</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ronlán</surname>
<given-names>Alvin</given-names></name>
<name><surname>Parker</surname>
<given-names>Vernon D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3214</fpage>
<lpage>3218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003214">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003214">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of isocoumarin chemistry. Part I. A synthesis of berbine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003219</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. W.</given-names></name>
<name><surname>Dyke</surname>
<given-names>S. F.</given-names></name>
<name><surname>Sainsbury</surname>
<given-names>M.</given-names></name>
<name><surname>Hardy</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3219</fpage>
<lpage>3222</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003219">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003219">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part XVIII. A second stereospecific &lt;i&gt;cis&lt;/i&gt;-addition of the elements of nitromethane across a tetrasubstituted ethylenic double bond. A concerted mechanism for the reaction of nitroacetic acid with enamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003222</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Kobayashi</surname>
<given-names>Toshihiko</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3222</fpage>
<lpage>3229</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003222">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003222">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis of oligoribonucleotides. Part IX. Preparation of ribonucleoside 2′-acetal 5′-esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boom</surname>
<given-names>J. H. van</given-names></name>
<name><surname>Owen</surname>
<given-names>G. R.</given-names></name>
<name><surname>Preston</surname>
<given-names>J.</given-names></name>
<name><surname>Ravindranathan</surname>
<given-names>T.</given-names></name>
<name><surname>Reese</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3230</fpage>
<lpage>3237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aminopyrrolo[1,2-&lt;i&gt;c&lt;/i&gt;]pyrimidines. A novel ring cleavage</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003237</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irwin</surname>
<given-names>W. J.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3237</fpage>
<lpage>3239</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003237">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003237">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of arylcyclohexadienyl radicals: rearrangement &lt;i&gt;versus&lt;/i&gt; fragmentation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003240</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>D. J.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
<name><surname>Ward</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3240</fpage>
<lpage>3247</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003240">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003240">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation and rearrangement of 6,6-diphenylbicyclo[3,1,0]hex-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003247</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>D. J.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
<name><surname>Ward</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3247</fpage>
<lpage>3251</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003247">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003247">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses of di-, tri-, and tetra-cyclopropylethylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003252</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Teraji</surname>
<given-names>Tsutomu</given-names></name>
<name><surname>Moritani</surname>
<given-names>Ichiro</given-names></name>
<name><surname>Tsuda</surname>
<given-names>Emako</given-names></name>
<name><surname>Nishida</surname>
<given-names>Shinya</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3252</fpage>
<lpage>3257</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003252">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003252">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reductive acylation of 5-nitropyridines with anhydrides of acetic, phthalic, and succinic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003257</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>G. H.</given-names></name>
<name><surname>Rickard</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3257</fpage>
<lpage>3260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003257">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003257">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Strecker degradation of α-amino-acids with benzil and with benzoin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003260</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Sayyab</surname>
<given-names>A. F.</given-names></name>
<name><surname>Atto</surname>
<given-names>A. T.</given-names></name>
<name><surname>Sarah</surname>
<given-names>F. Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3260</fpage>
<lpage>3261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003260">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003260">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2-Benzisothiazoles. Part I. Reaction of 3-chloro-1,2-benzisothiazole with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carrington</surname>
<given-names>D. E. L.</given-names></name>
<name><surname>Clarke</surname>
<given-names>K.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3262</fpage>
<lpage>3265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photorearrangement of 6-acetoxy-3,5-bis(chloromethyl)-2,4,6-trimethylcyclohexa-2,4-dienone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003266</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morris</surname>
<given-names>M. R.</given-names></name>
<name><surname>Waring</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3266</fpage>
<lpage>3269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003266">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003266">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereospecific photoisomerisations of 6-acetoxy-2,3,4,5,6-pentamethylcyclohexa-2,4-dienone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morris</surname>
<given-names>M. R.</given-names></name>
<name><surname>Waring</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3269</fpage>
<lpage>3274</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereoselective photochemical ring-opening of cyclohexa-2,4-dienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003274</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waring</surname>
<given-names>A. J.</given-names></name>
<name><surname>Morris</surname>
<given-names>M. R.</given-names></name>
<name><surname>Islam</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3274</fpage>
<lpage>3280</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003274">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003274">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic quaternary ammonium salts. Part IX. 1,1′-Azoimidazo[1,2-&lt;i&gt;a&lt;/i&gt;]-pyridinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003280</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glover</surname>
<given-names>E. E.</given-names></name>
<name><surname>Yorke</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3280</fpage>
<lpage>3285</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003280">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003280">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition reactions of heterocyclic compounds. Part XLIV. The synthesis and photoisomerism of some quinolizine esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003285</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Stubbs</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3285</fpage>
<lpage>3291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003285">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003285">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition reactions of heterocyclic compounds. Part XLV. New azepines from substituted 2-methylquinolines and dialkyl acetylenedicarboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003291</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Nisbet</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3291</fpage>
<lpage>3296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003291">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003291">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition reactions of heterocyclic compounds. Part XLVI. Reactions of acetylenic esters with pyridines in the presence of proton donors, and with alkyl 3-(2-pyridyl)-&lt;i&gt;trans&lt;/i&gt;-acrylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003296</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Woollard</surname>
<given-names>J. Mck.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3296</fpage>
<lpage>3305</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003296">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003296">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metallation of 1,3-bistrifluoromethylbenzene and &lt;i&gt;NN&lt;/i&gt;-dimethyl-3,5-bistrifluoromethylaniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grocock</surname>
<given-names>D. E.</given-names></name>
<name><surname>Jones</surname>
<given-names>T. K.</given-names></name>
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
<name><surname>Hepworth</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3305</fpage>
<lpage>3308</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Natural acetylenes. Part XXXIII. The biogenesis of the C&lt;sub&gt;9&lt;/sub&gt; diacetylenic triol from the fungus &lt;i&gt;Clitocybe rhizophora&lt;/i&gt; velen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003308</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barley</surname>
<given-names>G. C.</given-names></name>
<name><surname>Day</surname>
<given-names>A. C.</given-names></name>
<name><surname>Graf</surname>
<given-names>U.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>O'Neill</surname>
<given-names>I.</given-names></name>
<name><surname>Tachikawa</surname>
<given-names>R.</given-names></name>
<name><surname>Thaller</surname>
<given-names>V.</given-names></name>
<name><surname>Hodge</surname>
<given-names>R. A. Vere</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3308</fpage>
<lpage>3313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1-Methylsulphonyl- and 1-phenylsulphonyl-indazolin-3-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003313</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Leverett</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3313</fpage>
<lpage>3314</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses of a proerythrinadienone by phenolic oxidation and a morphinandienone system by a photo-pschorr reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003315</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Charubala</surname>
<given-names>R.</given-names></name>
<name><surname>Ihara</surname>
<given-names>M.</given-names></name>
<name><surname>Koizumi</surname>
<given-names>M.</given-names></name>
<name><surname>Takahashi</surname>
<given-names>K.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3315</fpage>
<lpage>3318</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003315">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003315">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A total synthesis of (±)-Kikemanine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003318</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Honda</surname>
<given-names>T.</given-names></name>
<name><surname>Ihara</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3318</fpage>
<lpage>3321</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003318">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003318">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitroxide radicals. Part XI. Polymerisation of t-butyl vinylphenyl nitroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003322</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forrester</surname>
<given-names>A. R.</given-names></name>
<name><surname>Hepburn</surname>
<given-names>S. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3322</fpage>
<lpage>3328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003322">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003322">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some thermal and photo-reactions of benzo- and naphtho-furandiones (coumarandiones)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003328</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Khandelwal</surname>
<given-names>G. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3328</fpage>
<lpage>3331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003328">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003328">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>γγ-Disubstituted itaconic acids. Part VI. The stobbe condensation of aryl cyclohexyl ketones and &lt;i&gt;o&lt;/i&gt;-methylbenzophenone with dimethyl succinate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003332</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>El-Newaihy</surname>
<given-names>M. F.</given-names></name>
<name><surname>Ayoub</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3332</fpage>
<lpage>3338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The boron trifluoride-catalysed reaction of furan derivatives with ethane-1,2-dithiol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rindone</surname>
<given-names>B.</given-names></name>
<name><surname>Scolastico</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3339</fpage>
<lpage>3341</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsymmetrically disubstituted ferrocenes. Part XI. The effect of solvent and metallating agent on the lithiation of 2-ferrocenylpyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003341</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>D. J.</given-names></name>
<name><surname>Rockett</surname>
<given-names>B. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3341</fpage>
<lpage>3344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003341">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003341">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of tautomerism. Part III. A new dimerisation reaction of pseudo-acid chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhatt</surname>
<given-names>M. V.</given-names></name>
<name><surname>Kamath</surname>
<given-names>K. M.</given-names></name>
<name><surname>Ravindranathan</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3344</fpage>
<lpage>3347</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Friedel–Crafts acylations of aromatic hydrocarbons. Part XII. Acetylation and benzoylation of 1,4-dimethylnaphthalene and 1,2,3,4-tetramethylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Hoskins</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3347</fpage>
<lpage>3350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003347">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CDXXI. General synthesis of 7,8-dioxygenated 1-benzyl-1,2,3,4-tetrahydroisoquinolines and elucidation of the structure of caseadine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003350</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Nakano</surname>
<given-names>T.</given-names></name>
<name><surname>Shishido</surname>
<given-names>K.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3350</fpage>
<lpage>3354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003350">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003350">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Methylation of reducing carbohydrates. Permethylated derivatives of melibiose [&lt;i&gt;O&lt;/i&gt;-α-D-galactopyranosyl-(1 &lt;b&gt;→&lt;/b&gt; 6)-D-glucopyranose]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003354</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gelpi</surname>
<given-names>María E.</given-names></name>
<name><surname>Deferrari</surname>
<given-names>Jorge O.</given-names></name>
<name><surname>Cadenas</surname>
<given-names>Raúl A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3354</fpage>
<lpage>3357</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003354">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003354">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituted oxindoles. Part V. Synthesis and stereochemistry of some substituted 3-benzylidene-1-methylindol-2(3&lt;i&gt;H&lt;/i&gt;)-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003357</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Daisley</surname>
<given-names>R. W.</given-names></name>
<name><surname>Walker</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3357</fpage>
<lpage>3363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003357">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003357">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical reactions of chlorobenzene derivatives in benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003363</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robinson</surname>
<given-names>G. E.</given-names></name>
<name><surname>Vernon</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3363</fpage>
<lpage>3367</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003363">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003363">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Coumarin and related compounds. Part XIV. A novel 4-methoxy-1-naphthyl 4-methoxy-1-naphthylethyl ketone from the aluminium chloride-catalysed reaction of 1-methoxynaphthalene with acrylonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003367</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gupta</surname>
<given-names>Arun K. Das</given-names></name>
<name><surname>Chatterje</surname>
<given-names>Rabindra M.</given-names></name>
<name><surname>Paul</surname>
<given-names>Madhusudan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3367</fpage>
<lpage>3370</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003367">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003367">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pinacol-type rearrangements in the phenylcyclohexane series: evidence for differences between the reaction mechanisms of epoxides and of the corresponding diols and halogenohydrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berti</surname>
<given-names>G.</given-names></name>
<name><surname>Macchia</surname>
<given-names>B.</given-names></name>
<name><surname>Macchia</surname>
<given-names>F.</given-names></name>
<name><surname>Monti</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3371</fpage>
<lpage>3375</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis of neoclovene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McKillop</surname>
<given-names>T. F. W.</given-names></name>
<name><surname>Martin</surname>
<given-names>J.</given-names></name>
<name><surname>Parker</surname>
<given-names>W.</given-names></name>
<name><surname>Roberts</surname>
<given-names>J. S.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3375</fpage>
<lpage>3384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroheterocyclic compounds. Part XXI. Thermal rearrangement of perfluoropyridazine and perfluoroalkylpyridazines to pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>MacBride</surname>
<given-names>J. A. H.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3384</fpage>
<lpage>3388</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extractives from poisonous British plants. Part I. The structure of alpinumisoflavone, a new pyranoisoflavone from &lt;i&gt;Laburnum alpinum&lt;/i&gt; J. Presl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003389</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jackson</surname>
<given-names>B.</given-names></name>
<name><surname>Owen</surname>
<given-names>P. J.</given-names></name>
<name><surname>Scheinmann</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3389</fpage>
<lpage>3392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003389">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003389">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of peptides containing &lt;i&gt;N&lt;/i&gt;-2-aminoethylglycine—‘reduction analogues’</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003393</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atherton</surname>
<given-names>E.</given-names></name>
<name><surname>Law</surname>
<given-names>H. D.</given-names></name>
<name><surname>Moore</surname>
<given-names>S.</given-names></name>
<name><surname>Elliott</surname>
<given-names>D. F.</given-names></name>
<name><surname>Wade</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3393</fpage>
<lpage>3396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003393">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003393">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photodimerisation of 2-benzyl-5-&lt;i&gt;p&lt;/i&gt;-bromobenzylidenecyclopentanone, a crystal–crystal transformation: &lt;i&gt;X&lt;/i&gt;-ray study of the dimer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003396</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3396</fpage>
<lpage>3398</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003396">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003396">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Abnormal addition of free radicals to sterically hindered nitrosobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003399</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hosogai</surname>
<given-names>Takeo</given-names></name>
<name><surname>Inamoto</surname>
<given-names>Naoki</given-names></name>
<name><surname>Okazaki</surname>
<given-names>Renji</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3399</fpage>
<lpage>3401</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003399">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003399">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of 1-methyl-2′-(&lt;i&gt;p&lt;/i&gt;-tolylsulphonamido)-2-(&lt;i&gt;p&lt;/i&gt;-tolylsulphonylimino)indoline-3-spirocyclopentane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tickle</surname>
<given-names>I. J.</given-names></name>
<name><surname>Prout</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3401</fpage>
<lpage>3405</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substitution reactions of benzo[&lt;i&gt;b&lt;/i&gt;]thiophen derivatives. Part III. Nitration of benzo[&lt;i&gt;b&lt;/i&gt;]thiophen-2-carboxylic acid and its 3-methyl derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>J.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3405</fpage>
<lpage>3409</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Total syntheses of racemic fukinone and of natural (+)-hydroxyeremophilone.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pinder</surname>
<given-names>A. R.</given-names></name>
<name><surname>Torrence</surname>
<given-names>Alan K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3410</fpage>
<lpage>3414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of[1-&lt;sup&gt;3&lt;/sup&gt;H]ergosterol and [1-&lt;sup&gt;3&lt;/sup&gt;H]ergocalciferol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003415</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pelc</surname>
<given-names>B.</given-names></name>
<name><surname>Kodicek</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3415</fpage>
<lpage>3418</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003415">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003415">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azonia-azulene salts. Part III. The thermal decomposition of &lt;i&gt;o&lt;/i&gt;-benzylphenyl azides to give azepinoindoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003418</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cliff</surname>
<given-names>G. R.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3418</fpage>
<lpage>3425</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003418">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003418">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azonia-azulene salts. Part IV. Attempts to convert dihydroindolizines into azonia-azulenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003426</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cliff</surname>
<given-names>G. R.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
<name><surname>Stanyer</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3426</fpage>
<lpage>3427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003426">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003426">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some addition reactions of 1,2,3,4,7,7-hexachloronorborna-2,5-diene, 1,4,5,6,7,7-hexachloronorborn-5-en-2-one, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Mason</surname>
<given-names>Patricia</given-names></name>
<name><surname>Parrott</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3428</fpage>
<lpage>3437</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Formation of &lt;i&gt;N&lt;/i&gt;-mono- and &lt;i&gt;NN&lt;/i&gt;-di-benzoyl amines by benzoylation of phosphoramidate and related anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003437</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Moran</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3437</fpage>
<lpage>3441</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003437">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003437">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction products from αβ-unsaturated ketones and aliphatic diamines or dithiols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003441</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hideg</surname>
<given-names>Kálmán</given-names></name>
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3441</fpage>
<lpage>3445</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003441">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003441">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical synthesis at low temperatures. Part III. Ready synthesis of bicyclo[4,2,0]octan-2-ones from cyclohexenones and ethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003445</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Owsley</surname>
<given-names>Dennis C.</given-names></name>
<name><surname>Bloomfield</surname>
<given-names>Jordan J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3445</fpage>
<lpage>3447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003445">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003445">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Condensed thiophen ring systems. Part VII. Stability of 3-benzo[&lt;i&gt;b&lt;/i&gt;]-thienyl-lithium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003447</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dickinson</surname>
<given-names>R. P.</given-names></name>
<name><surname>Iddon</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3447</fpage>
<lpage>3454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003447">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003447">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of novel macrocyclic compounds containing sulphur or oxygen in the ring: thia- and oxa-cyclophanes. Mass spectral and other studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>David W.</given-names></name>
<name><surname>Braunton</surname>
<given-names>Peter N.</given-names></name>
<name><surname>Millar</surname>
<given-names>Ian T.</given-names></name>
<name><surname>Tebby</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3454</fpage>
<lpage>3466</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis and rearrangement reactions of α-bromophenacyl 'onium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003467</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laird</surname>
<given-names>T.</given-names></name>
<name><surname>Williams</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3467</fpage>
<lpage>3471</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003467">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003467">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bromomethyl 'onium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003471</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laird</surname>
<given-names>T.</given-names></name>
<name><surname>Williams</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3471</fpage>
<lpage>3474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003471">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003471">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of 2-methyl-2-nitrosopropane and related species with organoboranes: a ready &lt;i&gt;cis&lt;/i&gt;-elimination of alkene from trialkylboranes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003475</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foot</surname>
<given-names>K. G.</given-names></name>
<name><surname>Roberts</surname>
<given-names>B. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3475</fpage>
<lpage>3479</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosensitised decarboxylation of carboxylic acids by aromatic ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003480</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Harrison</surname>
<given-names>K.</given-names></name>
<name><surname>Steiner</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3480</fpage>
<lpage>3482</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003480">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003480">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosensitised oxidation of amines. Part IV. The use of aromatic hydrocarbons as sensitisers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003482</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartholomew</surname>
<given-names>R. F.</given-names></name>
<name><surname>Brimage</surname>
<given-names>D. R. G.</given-names></name>
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3482</fpage>
<lpage>3484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003482">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003482">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A search for 1,6-didehydro[10]annulenes as reactive intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003485</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alder</surname>
<given-names>R. W.</given-names></name>
<name><surname>Edley</surname>
<given-names>D. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3485</fpage>
<lpage>3487</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003485">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003485">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mycological chemistry. Part XXVII. Reinvestigation of the structure of purpurogenone, a metabolite of &lt;i&gt;Penicillium purpurogenum&lt;/i&gt; Stoll</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003488</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
<name><surname>Thompson</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3488</fpage>
<lpage>3492</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003488">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003488">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mycological chemistry. Part XXVIII. Isolation and structure of deoxypurpurogenone, a minor pigment of &lt;i&gt;Penicillium purpurogenum&lt;/i&gt; Stoll</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003493</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
<name><surname>Thompson</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3493</fpage>
<lpage>3495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003493">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003493">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The bromination of some derivatives of resorcinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003495</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cannon</surname>
<given-names>J. R.</given-names></name>
<name><surname>Cresp</surname>
<given-names>T. M.</given-names></name>
<name><surname>Metcalf</surname>
<given-names>B. W.</given-names></name>
<name><surname>Sargent</surname>
<given-names>M. V.</given-names></name>
<name><surname>Vinciguerra</surname>
<given-names>G.</given-names></name>
<name><surname>Elix</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3495</fpage>
<lpage>3504</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003495">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003495">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroid boranes. Part IV. Hydroboration of a steroid olefin with asymmetric boranes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003504</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Herz</surname>
<given-names>J. E.</given-names></name>
<name><surname>Márquez</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3504</fpage>
<lpage>3506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003504">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003504">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Compounds related to 1-hydroxymethylindane-2-carboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peacock</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3506</fpage>
<lpage>3510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;o&lt;/i&gt;-Nitroaniline derivatives. Part II. Reactions of nucleophiles with &lt;i&gt;N&lt;/i&gt;-benzylidene-&lt;i&gt;o&lt;/i&gt;-nitroaniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003510</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marshall</surname>
<given-names>R.</given-names></name>
<name><surname>Smith</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3510</fpage>
<lpage>3514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003510">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003510">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1-Phenethylisoquinoline alkaloids. Part II. The structures of alkaloids from &lt;i&gt;Colchicum cornigerum&lt;/i&gt;(Sweinf.) Tackh. et Drar</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ramage</surname>
<given-names>R.</given-names></name>
<name><surname>Cameron</surname>
<given-names>A. F.</given-names></name>
<name><surname>Hannaway</surname>
<given-names>C.</given-names></name>
<name><surname>Šantavý</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3514</fpage>
<lpage>3518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectra of organomercury compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Breuer</surname>
<given-names>S. W.</given-names></name>
<name><surname>Fear</surname>
<given-names>T. E.</given-names></name>
<name><surname>Lindsay</surname>
<given-names>P. H.</given-names></name>
<name><surname>Thorpe</surname>
<given-names>F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3519</fpage>
<lpage>3524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dehydration of 4-hydroxy-2,3,4-triphenylcyclopent-2-enone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3524</fpage>
<lpage>3531</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>15&lt;i&gt;H&lt;/i&gt;-cyclohepta[2,1-&lt;i&gt;a&lt;/i&gt;:4,5-&lt;i&gt;a&lt;/i&gt;′]dinaphthalen-15-one. The condensation of naphthalene-1,2-dicarboxylic anhydride with 2-naphthylacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003532</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Agranat</surname>
<given-names>Israel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3532</fpage>
<lpage>3536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003532">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003532">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azabenzocycloheptenones. Part XIII. Ring expansion of 1,2-dihydroquinoline derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cromarty</surname>
<given-names>A.</given-names></name>
<name><surname>Haque</surname>
<given-names>K. E.</given-names></name>
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3536</fpage>
<lpage>3540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transformations of penicillin. Part I. Preparation and rearrangements of 6β-phenylacetamidopenicillanic sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Comer</surname>
<given-names>F.</given-names></name>
<name><surname>Greig</surname>
<given-names>D. G. T.</given-names></name>
<name><surname>Sammes</surname>
<given-names>P. G.</given-names></name>
<name><surname>Cooper</surname>
<given-names>(Mrs.) C. M.</given-names></name>
<name><surname>Hewitt</surname>
<given-names>G.</given-names></name>
<name><surname>Underwood</surname>
<given-names>W. G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3540</fpage>
<lpage>3550</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of alkyl and aryl thiosulphenimides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003550</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Behforouz</surname>
<given-names>Mohammad</given-names></name>
<name><surname>Firouzabadi</surname>
<given-names>Habib</given-names></name>
<name><surname>Ardakani</surname>
<given-names>Ali Afzali</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3550</fpage>
<lpage>3551</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in the synthesis of camptothecin. An efficient synthesis of 2,3-dihydro-1&lt;i&gt;H&lt;/i&gt;-pyrrolo[3,4-&lt;i&gt;b&lt;/i&gt;]quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003551</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zalkow</surname>
<given-names>L. H.</given-names></name>
<name><surname>Nabors</surname>
<given-names>J. B.</given-names></name>
<name><surname>French</surname>
<given-names>K.</given-names></name>
<name><surname>Bisarya</surname>
<given-names>S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3551</fpage>
<lpage>3554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003551">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003551">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;sup&gt;1&lt;/sup&gt;H–&lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance decoupling by paramagnetic ion co-ordination at nitrogen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Engel</surname>
<given-names>Robert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3554</fpage>
<lpage>3557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LIX. The synthesis of (±)-ascochitine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003557</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Galbraith</surname>
<given-names>M. N.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3557</fpage>
<lpage>3559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003557">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003557">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LX. The synthesis of tetrahydrosclerotioramine, tetrahydrosclerotoquinone, and tetrahydrosclerotiorin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003559</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birchall</surname>
<given-names>G. R.</given-names></name>
<name><surname>Galbraith</surname>
<given-names>M. N.</given-names></name>
<name><surname>Gray</surname>
<given-names>R. W.</given-names></name>
<name><surname>King</surname>
<given-names>R. R.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3559</fpage>
<lpage>3566</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003559">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003559">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LXI. The synthesis of (±)-sclerotiorin, of (±)-4,6-dimethylocta-&lt;i&gt;trans&lt;/i&gt;-2,&lt;i&gt;trans&lt;/i&gt;-4-dienoic acid, and of an analogue of rotiorin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003566</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chong</surname>
<given-names>R.</given-names></name>
<name><surname>King</surname>
<given-names>R. R.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3566</fpage>
<lpage>3571</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003566">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003566">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LXII. The synthesis of (±)-mitorubrin, a metabolite of &lt;i&gt;Penicillium rubrum&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003571</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chong</surname>
<given-names>R.</given-names></name>
<name><surname>Gray</surname>
<given-names>R. W.</given-names></name>
<name><surname>King</surname>
<given-names>R. R.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3571</fpage>
<lpage>3575</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003571">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003571">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LXIII. Rubrorotiorin, a metabolite of &lt;i&gt;Penicillium hirayamae&lt;/i&gt; Udagawa</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003575</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>R. W.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3575</fpage>
<lpage>3577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003575">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003575">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LXIV. The structure of monascin: the relative stereochemistry of the azaphilones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chen</surname>
<given-names>F. C.</given-names></name>
<name><surname>Manchand</surname>
<given-names>P. S.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3577</fpage>
<lpage>3579</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LXV. The structures of ergochrysin A, isoergochrysin A, and ergoxanthin, and of secalonic acids A, B, C, and D</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003580</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hooper</surname>
<given-names>J. W.</given-names></name>
<name><surname>Marlow</surname>
<given-names>W.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
<name><surname>Borthwick</surname>
<given-names>A. D.</given-names></name>
<name><surname>Bowden</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3580</fpage>
<lpage>3590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003580">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003580">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of fungi. Part LXVI. A new synthesis of isoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahmad</surname>
<given-names>S.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3590</fpage>
<lpage>3593</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Factors in the formation of isomerically and optically pure alkyl halides. Part VIII. Rearrangements in the reactions of branched-chain alcohols with boron trichloride and boron tribromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>H. R.</given-names></name>
<name><surname>Kinghorn</surname>
<given-names>R. R. F.</given-names></name>
<name><surname>Murphy</surname>
<given-names>W. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3593</fpage>
<lpage>3596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Partially fluorinated heterocyclic compounds. Part IX. The syntheses of 4,5,6,7-tetrafluorobenzo[&lt;i&gt;b&lt;/i&gt;]furan and 4,5,6,7-tetrafluoro-2-phenylbenzo[&lt;i&gt;b&lt;/i&gt;]furan by a new cyclisation reaction, and the attempted syntheses of related compounds by conventional methods</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003596</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooke</surname>
<given-names>G. M.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
<name><surname>Thomas</surname>
<given-names>T. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3596</fpage>
<lpage>3599</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003596">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003596">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New intermediates and dyestuffs for synthetic fibres. Part IV. 2-Nitronaphthalene-1,8-dicarboxylic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003599</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grayshan</surname>
<given-names>P. H.</given-names></name>
<name><surname>Peters</surname>
<given-names>A. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3599</fpage>
<lpage>3600</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003599">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003599">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New intermediates and dyestuffs for synthetic fibres. Part V. By-products of the Ullmann condensation between 1-chloroanthraquinone and aniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003600</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lord</surname>
<given-names>W. M.</given-names></name>
<name><surname>Peters</surname>
<given-names>A. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3600</fpage>
<lpage>3601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003600">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003600">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2,3,5,6-Tetrahydro- and 5,6-dihydro-imidazo[2,1-&lt;i&gt;b&lt;/i&gt;]thiazoles from imidazoline-2-thiol derivatives and unsaturated or halogenated acids and esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003602</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackshire</surname>
<given-names>R. B.</given-names></name>
<name><surname>Sharpe</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3602</fpage>
<lpage>3605</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003602">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003602">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Approaches to heterocyclic analogues of biphenylene. Part II. Some 5,5′6,6′-tetraphenyl-2,2′-bipyrazinyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003605</article-id><contrib-group><contrib contrib-type="author">
<name><surname>England</surname>
<given-names>P.</given-names></name>
<name><surname>McDougall</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3605</fpage>
<lpage>3611</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003605">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003605">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;trans&lt;/i&gt;-1,2-Dichlorocyclohexane from the interaction of benzenesulphonyl chloride and cyclohexene in the presence of aluminium chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003611</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holt</surname>
<given-names>G.</given-names></name>
<name><surname>Jeffreys</surname>
<given-names>K. D.</given-names></name>
<name><surname>Jeffreys</surname>
<given-names>P. D.</given-names></name>
<name><surname>Tonietti</surname>
<given-names>S. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3611</fpage>
<lpage>3614</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003611">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003611">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phosphorylation of diamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003614</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3614</fpage>
<lpage>3617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003614">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003614">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CDXXXII. Synthesis of (±)-thalicsimidine by a possible biosynthetic route</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003617</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Takahashi</surname>
<given-names>K.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3617</fpage>
<lpage>3620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003617">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003617">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel homophthalimide (isoquinoline-1,3-dione) derivatives obtained by addition–cyclisation reactions of nona-2,7-diynedioic acid derivatives with methylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003620</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McCorkindale</surname>
<given-names>N. J.</given-names></name>
<name><surname>Magrill</surname>
<given-names>D. S.</given-names></name>
<name><surname>Raphael</surname>
<given-names>R. A.</given-names></name>
<name><surname>Wright</surname>
<given-names>J. L. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3620</fpage>
<lpage>3626</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003620">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003620">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactivity of pseudoaromatic compounds. Part III. Reactions of 2-lodo-, 2-bromo-, and 2-choloro-tropone with quinuclidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003626</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pietra</surname>
<given-names>Francesco</given-names></name>
<name><surname>Biggi</surname>
<given-names>Gino</given-names></name>
<name><surname>Cima</surname>
<given-names>Francesco Del</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3626</fpage>
<lpage>3630</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003626">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003626">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 2,2-dialkyl-1,2-dihydroquinolines. Part VI. Further bromination studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. P.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3631</fpage>
<lpage>3634</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Constitution and absolute configuration of &lt;i&gt;meta&lt;/i&gt;,&lt;i&gt;meta&lt;/i&gt;-bridged, strained biphenyls from &lt;i&gt;Myrica nagi&lt;/i&gt;; &lt;i&gt;X&lt;/i&gt;-ray analysis of 16-bromomyricanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003634</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Begley</surname>
<given-names>M. J.</given-names></name>
<name><surname>Campbell</surname>
<given-names>R. V. M.</given-names></name>
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Tuck</surname>
<given-names>B.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3634</fpage>
<lpage>3642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003634">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003634">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2,3-Benzothiadiazoles. Part IV. The rearrangement of diazonium salts derived from 7-aminobenzothiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haddock</surname>
<given-names>E.</given-names></name>
<name><surname>Kirby</surname>
<given-names>P.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3642</fpage>
<lpage>3644</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dichloroketen adducts of 6,6-diphenylfulvene and 8,8-diphenylbenzofulvene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003645</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harmon</surname>
<given-names>Robert E.</given-names></name>
<name><surname>Barta</surname>
<given-names>William D.</given-names></name>
<name><surname>Gupta</surname>
<given-names>S. K.</given-names></name>
<name><surname>Slomp</surname>
<given-names>George</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3645</fpage>
<lpage>3650</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003645">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003645">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of the benzo[&lt;i&gt;c&lt;/i&gt;]quinolizinium system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003650</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fozard</surname>
<given-names>Alan</given-names></name>
<name><surname>Davies</surname>
<given-names>L. S.</given-names></name>
<name><surname>Bradsher</surname>
<given-names>C. K.</given-names></name>
<name><surname>Gross</surname>
<given-names>Paul M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3650</fpage>
<lpage>3652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003650">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003650">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A selective bromination of aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caló</surname>
<given-names>V.</given-names></name>
<name><surname>Ciminale</surname>
<given-names>F.</given-names></name>
<name><surname>Lopez</surname>
<given-names>L.</given-names></name>
<name><surname>Todesco</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3652</fpage>
<lpage>3653</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Circular dichroism of pyrrolizidine alkaloids and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003653</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Culvenor</surname>
<given-names>C. C. J.</given-names></name>
<name><surname>Crout</surname>
<given-names>D. H. G.</given-names></name>
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Mose</surname>
<given-names>W. P.</given-names></name>
<name><surname>Renwick</surname>
<given-names>J. D.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3653</fpage>
<lpage>3664</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ring expansion of prophins with ethoxycarbonylnitrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003664</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3664</fpage>
<lpage>3668</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003664">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003664">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;C&lt;/i&gt;-alkylation by 3-diazopropene, and the function of diazoalkanes as nitrogen bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003668</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clinging</surname>
<given-names>R.</given-names></name>
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3668</fpage>
<lpage>3671</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003668">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003668">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of cyclohexadienes. Part XII. Some dienamines and dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003671</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hutchinson</surname>
<given-names>E. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3671</fpage>
<lpage>3673</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003671">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003671">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structures of some hexa-1,5-diene-1,1,3,3,4,4,6,6-octacarboxylic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003673</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Hughes</surname>
<given-names>N. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3673</fpage>
<lpage>3679</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003673">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003673">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tetramethyl 2,2,4,4-tetramethoxycarbonylcyclobutane-1,3-dimalonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003679</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Hughes</surname>
<given-names>N. W.</given-names></name>
<name><surname>Sternhell</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3679</fpage>
<lpage>3681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003679">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003679">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of porphin analogues containing furan and/or thiophen rings</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003681</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Broadhurst</surname>
<given-names>M. J.</given-names></name>
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3681</fpage>
<lpage>3690</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003681">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003681">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic substitution of olefins. Part XVII. Reactions of ferrocene with olefins in the presence of palladium(II) salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003691</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Asano</surname>
<given-names>Ryuzo</given-names></name>
<name><surname>Moritani</surname>
<given-names>Ichiro</given-names></name>
<name><surname>Sonoda</surname>
<given-names>Akio</given-names></name>
<name><surname>Fujiwara</surname>
<given-names>Yuzo</given-names></name>
<name><surname>Teranishi</surname>
<given-names>Shiichiro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3691</fpage>
<lpage>3692</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003691">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003691">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses of heterocyclic compounds. Part XXIV. Cyclisation studies with &lt;i&gt;ortho&lt;/i&gt;-substituted arylcarbene and arylnitrene precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003693</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garner</surname>
<given-names>G. V.</given-names></name>
<name><surname>Mobbs</surname>
<given-names>D. B.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
<name><surname>Millership</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3693</fpage>
<lpage>3701</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003693">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003693">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Analysis of structural characteristics of chemical compounds in a large computer-based file. Part II. Atom-centred fragments</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003702</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adamson</surname>
<given-names>G. W.</given-names></name>
<name><surname>Lynch</surname>
<given-names>M. F.</given-names></name>
<name><surname>Town</surname>
<given-names>W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3702</fpage>
<lpage>3706</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003702">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003702">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6-Alkyl derivatives of 3-(3,4-dihydroxyphenyl)alanine (dopa). Part I. Synthesis &lt;i&gt;via&lt;/i&gt; oxazolinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003706</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morgenstern</surname>
<given-names>A. P.</given-names></name>
<name><surname>Schuijt</surname>
<given-names>C.</given-names></name>
<name><surname>Nauta</surname>
<given-names>W. Th.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3706</fpage>
<lpage>3712</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003706">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003706">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of nitro-compounds. Part I. Acid-catalysed ring-opening reactions of substituted &lt;i&gt;o&lt;/i&gt;-nitrophenylethylene oxides involving participation by the nitro-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spence</surname>
<given-names>T. W. M.</given-names></name>
<name><surname>Tennant</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3712</fpage>
<lpage>3719</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The aluminium chloride-catalysed decomposition of some &lt;i&gt;N&lt;/i&gt;-(3-bromopropyl)arylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003719</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deady</surname>
<given-names>L. W.</given-names></name>
<name><surname>Pirzada</surname>
<given-names>N.</given-names></name>
<name><surname>Topsom</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3719</fpage>
<lpage>3721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003719">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003719">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polycyclic aromatic compounds. The conversion of 1,1,4-triarylbuta-1,3-diene-2,3-dicarboxylic anhydrides and 1,4-diarylnaphthalene-2,3-dicarboxylic anhydrides into polycyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Awad</surname>
<given-names>W. I.</given-names></name>
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Omara</surname>
<given-names>Mahmoud A.</given-names></name>
<name><surname>Omran</surname>
<given-names>Sayed M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3721</fpage>
<lpage>3727</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003721">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XLI. New routes to 4-aminopteridines &lt;i&gt;via&lt;/i&gt; 3-(dimethylaminomethyleneamino)pyrazine-2-carbonitrile and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003727</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Ohta</surname>
<given-names>Kyuji</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3727</fpage>
<lpage>3730</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003727">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003727">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An alternative synthesis of 2β,3β,14α,17β-tetrahydroxy-5β-androst-7-en-6-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003730</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cochrane</surname>
<given-names>J. S.</given-names></name>
<name><surname>Hanson</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3730</fpage>
<lpage>3732</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003730">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003730">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical modification of trehalose. Part IX. The monobenzylidene acetal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003733</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Richardson</surname>
<given-names>A. C.</given-names></name>
<name><surname>Tarelli</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3733</fpage>
<lpage>3735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003733">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyano-13-epicobalamin (neovitamin B&lt;sub&gt;12&lt;/sub&gt;) and its relatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonnett</surname>
<given-names>R.</given-names></name>
<name><surname>Godfrey</surname>
<given-names>J. M.</given-names></name>
<name><surname>Math</surname>
<given-names>V. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3736</fpage>
<lpage>3743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and mass spectra of some 3-acylamino-2-piperidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003743</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clarke</surname>
<given-names>D. R.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3743</fpage>
<lpage>3748</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003743">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003743">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Light-induced and related reactions of quinones. Part VIII. Some (2-hydroxyalkyl)-, phenethyl-, (2-ethoxycarbonylethyl)-, and styryl-1,4-benzoquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003749</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bruce</surname>
<given-names>J. Malcolm</given-names></name>
<name><surname>Creed</surname>
<given-names>David</given-names></name>
<name><surname>Dawes</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3749</fpage>
<lpage>3756</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003749">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003749">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The total synthesis of a nuclear analogue of the penicillin—cephalosporin antibiotics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brunwin</surname>
<given-names>D. M.</given-names></name>
<name><surname>Lowe</surname>
<given-names>G.</given-names></name>
<name><surname>Parker</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3756</fpage>
<lpage>3762</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Syntheses of L-vallarose (6-deoxy-3-&lt;i&gt;O&lt;/i&gt;-methyl-L-altrose) and D-digitalose (6-deoxy-3-&lt;i&gt;O&lt;/i&gt;-methyl-D-galactose)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Da'Aboul</surname>
<given-names>I.</given-names></name>
<name><surname>Tucker</surname>
<given-names>L. C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3762</fpage>
<lpage>3765</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hypoiodite reaction: the decomposition of oxalic acid half-esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003766</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartel</surname>
<given-names>K.</given-names></name>
<name><surname>Goosen</surname>
<given-names>A.</given-names></name>
<name><surname>Scheffer</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3766</fpage>
<lpage>3769</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003766">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003766">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of arenesulphonyl azides with some di- and tri-substituted indoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003769</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Scattergood</surname>
<given-names>R.</given-names></name>
<name><surname>Warr</surname>
<given-names>(Mrs.) W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3769</fpage>
<lpage>3778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003769">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003769">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkaloids of daphnandra species. Part X. The structure of isotenuipine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bick</surname>
<given-names>I. R. C.</given-names></name>
<name><surname>Taylor</surname>
<given-names>W. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3779</fpage>
<lpage>3780</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of 1,3-diphenylalk-1-enes with butyl-lithium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003780</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burley</surname>
<given-names>J. W.</given-names></name>
<name><surname>Young</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3780</fpage>
<lpage>3783</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003780">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003780">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extractives from Guttiferae. Part XXI. The isolation and structure of nine coumarins from the bark of &lt;i&gt;Mammea africana&lt;/i&gt; G. Don</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003783</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carpenter</surname>
<given-names>I.</given-names></name>
<name><surname>McGarry</surname>
<given-names>E. J.</given-names></name>
<name><surname>Scheinmann</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3783</fpage>
<lpage>3790</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003783">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003783">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extractives from Guttiferae. Part XXII. The isolation and structure of four novel biflavanones from the heartwoods of &lt;i&gt;Garcinia buchananii&lt;/i&gt; Baker and &lt;i&gt;G. eugeniifolia&lt;/i&gt; Wall</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003791</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jackson</surname>
<given-names>B.</given-names></name>
<name><surname>Locksley</surname>
<given-names>H. D.</given-names></name>
<name><surname>Scheinmann</surname>
<given-names>F.</given-names></name>
<name><surname>Wolstenholme</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3791</fpage>
<lpage>3804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003791">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003791">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extractives from Guttiferae. Part XXIII. An unambiguous synthesis of 6-deoxyjacareubin and related 3,3- and 1,1-dimethylallyl and annulated xanthones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Locksley</surname>
<given-names>H. D.</given-names></name>
<name><surname>Quillinan</surname>
<given-names>A. J.</given-names></name>
<name><surname>Scheinmann</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3804</fpage>
<lpage>3814</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of hop constituents. Part XXXVIII. Alkenylation of 2-acylcyclohexane-1,3,5-triones and further evidence concerning the fine structure of hop β-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>M.</given-names></name>
<name><surname>Laws</surname>
<given-names>D. R. J.</given-names></name>
<name><surname>McGuinness</surname>
<given-names>J. D.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3814</fpage>
<lpage>3818</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the syntheses of heterocyclic compounds. Part CDXLIII. An alternative synthesis of (±)-glaziovine by photolysis and phenolic oxidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Nakano</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3818</fpage>
<lpage>3821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metallation reactions. Part X. Allylic metallation in the presence of amide groups: long range interactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003821</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glily-Terry</surname>
<given-names>S.</given-names></name>
<name><surname>Klein</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3821</fpage>
<lpage>3827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003821">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003821">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dimethylcarbodi-imide. Improved synthesis, cyclic trimer, and reaction with α-hydroxy-esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003827</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rapi</surname>
<given-names>G.</given-names></name>
<name><surname>Sbrana</surname>
<given-names>G.</given-names></name>
<name><surname>Gelsomini</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3827</fpage>
<lpage>3829</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003827">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003827">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroalkyl derivatives of nitrogen. Part XXX. Reaction of &lt;i&gt;N&lt;/i&gt;-chlorobistrifluoromethylamine with propene and vinyl fluoride and of &lt;i&gt;N&lt;/i&gt;-iodobistrifluoromethylamine with vinyl fluoride under ionic conditions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003829</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>G. L.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3829</fpage>
<lpage>3833</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003829">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003829">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroalkyl derivatives of nitrogen. Part XXXI. Reaction of &lt;i&gt;N&lt;/i&gt;-chloro- and &lt;i&gt;N&lt;/i&gt;-lodo-bistrifluoromethylamine with hexafluoropropene, trifluoroethylene, and vinyl fluoride under radical conditions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>G. L.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3833</fpage>
<lpage>3838</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organosilicon chemistry. Part VII. Reactions of bis(trimethylsilyl)-mercury with perfluoro-olefins and -acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003838</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fields</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Hubbard</surname>
<given-names>(Mrs.) A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3838</fpage>
<lpage>3843</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003838">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003838">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance decoupling by paramagnetic ion co-ordination at oxygen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003844</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Engel</surname>
<given-names>Robert</given-names></name>
<name><surname>Nathan</surname>
<given-names>Gene</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3844</fpage>
<lpage>3846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003844">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003844">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Seco-steroids. Part I. Some 2-(2-hydroxyethyl)cyclopentanols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003846</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brain</surname>
<given-names>E. G.</given-names></name>
<name><surname>Cassidy</surname>
<given-names>F.</given-names></name>
<name><surname>Constantine</surname>
<given-names>M. F.</given-names></name>
<name><surname>Hanson</surname>
<given-names>J. C.</given-names></name>
<name><surname>Tidy</surname>
<given-names>D. J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3846</fpage>
<lpage>3851</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003846">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003846">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of santonene. Part VII. The action of phosphorus trihalides on the santonins, santonene, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003851</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Rane</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3851</fpage>
<lpage>3856</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003851">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003851">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic reactions in melts and solids. Part VIII. Reactions of diacylanilines with monobasic and dibasic carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003856</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Michman</surname>
<given-names>M.</given-names></name>
<name><surname>Frenkel</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3856</fpage>
<lpage>3859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003856">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003856">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies related to penicillins. Part V. The conversion of 6β-phthalimidopenicillanic acid into cepham derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ramsay</surname>
<given-names>B. G.</given-names></name>
<name><surname>Stoodley</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3859</fpage>
<lpage>3864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies related to penicillins. Part VI. The conversion of penicillin V and 6-aminopenicillanic acid into cepham derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003864</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ramsay</surname>
<given-names>B. G.</given-names></name>
<name><surname>Stoodley</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3864</fpage>
<lpage>3867</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003864">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003864">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The sulphur(II)–nitrogen bond. Part III. The synthesis of the sulphur-(II)–nitrogen bond from sulphenates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003867</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armitage</surname>
<given-names>D. A.</given-names></name>
<name><surname>Clark</surname>
<given-names>M. J.</given-names></name>
<name><surname>Kinsey</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3867</fpage>
<lpage>3869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003867">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003867">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bromination of pyrrolo[1,2-&lt;i&gt;c&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003870</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irwin</surname>
<given-names>W. J.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
<name><surname>Cooper</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3870</fpage>
<lpage>3872</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003870">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003870">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The action of cyanamide on 1,3,4-oxadiazolium and pyrylium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003873</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Dando</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3873</fpage>
<lpage>3875</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003873">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003873">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of 4-benzylidene-1-butylpyrrolidine-2,3-diones with aromatic thiols and amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003875</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sugden</surname>
<given-names>J. K.</given-names></name>
<name><surname>Hogan</surname>
<given-names>J. E.</given-names></name>
<name><surname>Abbe</surname>
<given-names>N. J. Van</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3875</fpage>
<lpage>3878</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003875">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003875">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of nickel 1,19-dimethyltetradehydrocorrin salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003879</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hamilton</surname>
<given-names>A.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3879</fpage>
<lpage>3887</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003879">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003879">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Antibiotic 1233A: a fungal β-lactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003888</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aldridge</surname>
<given-names>D. C.</given-names></name>
<name><surname>Giles</surname>
<given-names>(the late) D.</given-names></name>
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3888</fpage>
<lpage>3891</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003888">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003888">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acenaphthene. Part II. The preparation of 3,4-diaminonaphthalene-1,8-dicarboxylic anhydride (3,4-diaminonaphthalic anhydride) and derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003891</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>L. A.</given-names></name>
<name><surname>Kim</surname>
<given-names>H. K.</given-names></name>
<name><surname>Watson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3891</fpage>
<lpage>3893</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003891">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003891">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 3,3,4,4-tetrafluorohexa-1,5-diene. Part I. Cycloadditions with tetrafluoroethylene and chlorotrifluoroethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003894</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Piccardi</surname>
<given-names>P.</given-names></name>
<name><surname>Modena</surname>
<given-names>M.</given-names></name>
<name><surname>Santoro</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3894</fpage>
<lpage>3898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003894">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003894">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mycological chemistry. Part XXIX. Total synthesis of (±)-&lt;i&gt;O&lt;/i&gt;-methylaversin [(±)-tri-&lt;i&gt;O&lt;/i&gt;-methylversicolorin B]: the structure of aversin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003899</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holmwood</surname>
<given-names>G. M.</given-names></name>
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3899</fpage>
<lpage>3902</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003899">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003899">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2-Benzisothiazoles. Part II. Reactions of 3-chloro-1,2-benzisothiazole with carbanions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003903</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carrington</surname>
<given-names>D. E. L.</given-names></name>
<name><surname>Clarke</surname>
<given-names>K.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3903</fpage>
<lpage>3906</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003903">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003903">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The π-route to substituted adamantanes. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003906</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Faulkner</surname>
<given-names>D.</given-names></name>
<name><surname>McKervey</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3906</fpage>
<lpage>3910</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003906">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003906">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organometallic diazoalkanes. Part II. Heterocyclic syntheses with the co-ordinated ligand CN&lt;sub&gt;2&lt;/sub&gt;&lt;sup&gt;2–&lt;/sup&gt;; reactions of trimethylstannyl- and trimethylsilyl-diazoalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003910</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
<name><surname>Poland</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3910</fpage>
<lpage>3914</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003910">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003910">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>5α-Cholestano[7,6-&lt;i&gt;c&lt;/i&gt;]pyrazole derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003914</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pelc</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>3914</fpage>
<lpage>3916</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39710003914">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J3/J39710003914">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and absorption spectra of 4,5-disubstituted pyridine-2,6-(1&lt;i&gt;H&lt;/i&gt;,5&lt;i&gt;H&lt;/i&gt;)-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39710003916</article-id><contrib-group><contrib contrib-type="author">
<name><surname