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<articles xmlns:xlink="http://www.w3.org/1999/xlink">
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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/J396700FP001</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J396700FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J396700FP001">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/J396700FP003</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J396700FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J396700FP003">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>Circular dichroism of &lt;i&gt;N&lt;/i&gt;-thiobenzoyl-L-α-amino-acids. Part III. Their circular dichroism through the near-ultraviolet wavelength range</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000001</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1</fpage>
<lpage>5</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Multimacrocyclic compounds. Part I. Novel triply bridged dibenzenoid cage compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000006</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>6</fpage>
<lpage>10</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Multimacrocyclic compounds. Part II. Pentabenzenoid cage compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>11</fpage>
<lpage>12</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Multimacrocyclic compounds. Part III. Attempts to prepare benzenoid cage compounds from novel polyacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000013</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>13</fpage>
<lpage>14</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000013">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000013">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photodimer of &lt;i&gt;p&lt;/i&gt;-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>Elijah H.</given-names></name>
<name><surname>Ginsburg</surname>
<given-names>David</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>15</fpage>
<lpage>20</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Trihalogenomethylbenzazoles. Part I. Formation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000020</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holan</surname>
<given-names>G.</given-names></name>
<name><surname>Samuel</surname>
<given-names>(Mrs.) E. L.</given-names></name>
<name><surname>Ennis</surname>
<given-names>B. C.</given-names></name>
<name><surname>Hinde</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>20</fpage>
<lpage>25</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000020">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000020">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Trihalogenomethylbenzazoles. Part II. Reactions of 2-trihalogenomethylbenzimidazoles with ammonia and amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000025</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holan</surname>
<given-names>G.</given-names></name>
<name><surname>Samuel</surname>
<given-names>(Mrs.) E. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>25</fpage>
<lpage>29</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000025">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000025">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Trihalogenomethylbenzazoles. Part III. Reactions of 2-trichloromethylbenzimidazole with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ennis</surname>
<given-names>B. C.</given-names></name>
<name><surname>Holan</surname>
<given-names>G.</given-names></name>
<name><surname>Samuel</surname>
<given-names>(Mrs.) E. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>30</fpage>
<lpage>33</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Trihalogenomethylbenzazoles. Part IV. Reactions with difunctional nucleophiles. Formation of heterocyclic rings on the 2-position of benzazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000033</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ennis</surname>
<given-names>B. C.</given-names></name>
<name><surname>Holan</surname>
<given-names>G.</given-names></name>
<name><surname>Samuel</surname>
<given-names>(Mrs.) E. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>33</fpage>
<lpage>39</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000033">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000033">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. Methylation of substituted cinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Chapman</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>40</fpage>
<lpage>43</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Beckmann rearrangements of Mannich base and related oximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>MacConaill</surname>
<given-names>R. J.</given-names></name>
<name><surname>Riordan</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>44</fpage>
<lpage>47</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Some homolytic reactions of pentafluoroiodobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birchall</surname>
<given-names>J. M.</given-names></name>
<name><surname>Hazard</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Wakalski</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>47</fpage>
<lpage>50</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleosides. Part IV. &lt;i&gt;O&lt;/i&gt;- and &lt;i&gt;N&lt;/i&gt;-2′-amino-2′-deoxyglucopyranosides of cytosine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000051</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garg</surname>
<given-names>H. G.</given-names></name>
<name><surname>Ulbricht</surname>
<given-names>T. L. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>51</fpage>
<lpage>53</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000051">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000051">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. Tautomerism in polyfluorohydroxy-quinolines and -isoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000053</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>Storey</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>53</fpage>
<lpage>57</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Preparation and some reactions of 1,2,4,5-tetrahydro-1-oxo-3-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonylbenz[&lt;i&gt;d&lt;/i&gt;]azepine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000058</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rehman</surname>
<given-names>M. A.</given-names></name>
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>58</fpage>
<lpage>61</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000058">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000058">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 use of periodate-oxidised glycosides in the Robinson–Schöpf condensation: some analogues of 9-methyl-3-oxagranatan-7-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000062</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
<name><surname>McCarthy</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>62</fpage>
<lpage>66</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000062">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000062">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. Synthesis of two acetamidoethyl porphyrins and their conversion into vinyl porphyrins and chlorins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000066</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collier</surname>
<given-names>G. L.</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>66</fpage>
<lpage>72</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000066">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000066">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 displacement of all six fluorine atoms from hexafluorobenzene by sodium cyanide in methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000072</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wakefield</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>72</fpage>
<lpage>73</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000072">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000072">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. Some imidazo[4,5-&lt;i&gt;g&lt;/i&gt;]-benzoxazoles with a polymethylene bridge</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garner</surname>
<given-names>R.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>74</fpage>
<lpage>76</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphonhydrazides and related compounds. Part VII. Some substituted sulphanilyl hydrazides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000077</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>77</fpage>
<lpage>81</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000077">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000077">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 analogous to the &lt;i&gt;N&lt;/i&gt;-terminal eicosapeptide sequence of ribonuclease A. Part I. Synthesis of the orn&lt;sup&gt;10&lt;/sup&gt;-hexapeptide analogue of the sequence 7–12</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000081</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marchiori</surname>
<given-names>Fernando</given-names></name>
<name><surname>Rocchi</surname>
<given-names>Raniero</given-names></name>
<name><surname>Vidali</surname>
<given-names>Giorgio</given-names></name>
<name><surname>Tamburro</surname>
<given-names>Antonmario</given-names></name>
<name><surname>Scoffone</surname>
<given-names>Ernesto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>81</fpage>
<lpage>85</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000081">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000081">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 analogous to the &lt;i&gt;N&lt;/i&gt;-terminal eicosapeptide sequence of ribonuclease A. Part II. Synthesis of the Orn&lt;sup&gt;10&lt;/sup&gt;-dodecapeptide analogue of the sequence 1–12</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000086</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rocchi</surname>
<given-names>Raniero</given-names></name>
<name><surname>Marchiori</surname>
<given-names>Fernando</given-names></name>
<name><surname>Scatturin</surname>
<given-names>Angelo</given-names></name>
<name><surname>Scoffone</surname>
<given-names>Ernesto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>86</fpage>
<lpage>88</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000086">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000086">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 analogous to the &lt;i&gt;N&lt;/i&gt;-terminal eicosapeptide sequence of ribonuclease A. Part III. A new synthesis of the &lt;i&gt;C&lt;/i&gt;-terminal octapeptide 13–20</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000089</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marchiori</surname>
<given-names>Fernando</given-names></name>
<name><surname>Rocchi</surname>
<given-names>Raniero</given-names></name>
<name><surname>Moroder</surname>
<given-names>Luigi</given-names></name>
<name><surname>Vidali</surname>
<given-names>Giorgio</given-names></name>
<name><surname>Scoffone</surname>
<given-names>Ernesto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>89</fpage>
<lpage>91</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000089">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000089">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benzoyl isothiocyanate with hydrazine derivatives. Part I. Reaction with some alkyl hydrazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000092</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Durant</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>92</fpage>
<lpage>94</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000092">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000092">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 chromanone-type systems &lt;i&gt;via&lt;/i&gt; the acylation of derivatives of 2,6-dihydroxyanthracene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000095</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Schütz</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>95</fpage>
<lpage>99</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000095">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000095">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 acyl derivatives of 2,6-dimethoxyanthracene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Kingston</surname>
<given-names>D. G. I.</given-names></name>
<name><surname>Schütz</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>99</fpage>
<lpage>101</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bridged ring systems. Part X. The reductive rearrangement of δ-enol-lactones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000101</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>J.</given-names></name>
<name><surname>Parker</surname>
<given-names>W.</given-names></name>
<name><surname>Shroot</surname>
<given-names>B.</given-names></name>
<name><surname>Stewart</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>101</fpage>
<lpage>108</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000101">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000101">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peptides. Part XXIV. Syntheses of the &lt;i&gt;N&lt;/i&gt;-terminal pentapeptide and &lt;i&gt;C&lt;/i&gt;-terminal tetrapeptide sequences of porcine gastrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000108</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>J. C.</given-names></name>
<name><surname>Barton</surname>
<given-names>M. A.</given-names></name>
<name><surname>Hardy</surname>
<given-names>P. M.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Preston</surname>
<given-names>J.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>108</fpage>
<lpage>113</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000108">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000108">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alternative syntheses of 1-, 2-, and 3-&lt;i&gt;O&lt;/i&gt;-methyl-D-mannitol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000114</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bayne</surname>
<given-names>S.</given-names></name>
<name><surname>Fewster</surname>
<given-names>J. A.</given-names></name>
<name><surname>Grieve</surname>
<given-names>(the late) A. J.</given-names></name>
<name><surname>Hawksley</surname>
<given-names>(Miss) M. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>114</fpage>
<lpage>115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000114">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000114">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 aspects of the intramolecular cyclisation of 2-arylcyclohexylacetic acids. Part III</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bien</surname>
<given-names>Shlomo</given-names></name>
<name><surname>Michael</surname>
<given-names>Uri</given-names></name>
<name><surname>Zamir</surname>
<given-names>Lolita (Cohen)</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>115</fpage>
<lpage>119</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 ionisation constants of some fluorenamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000120</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davey</surname>
<given-names>J.</given-names></name>
<name><surname>Keene</surname>
<given-names>B. R. T.</given-names></name>
<name><surname>Mannering</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>120</fpage>
<lpage>123</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000120">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000120">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phenylacetonitrile with carbon disulphide and the preparation of 4-aryl isothiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000124</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>Michael</given-names></name>
<name><surname>Snowling</surname>
<given-names>Geoffrey</given-names></name>
<name><surname>Winch</surname>
<given-names>Roger W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>124</fpage>
<lpage>124</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000124">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000124">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. A Diels–Alder adduct of a tetrahydropyranyloxycyclohexadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000125</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hill</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>125</fpage>
<lpage>126</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000125">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000125">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Use of ethoxyacetylene for the synthesis of &lt;i&gt;N&lt;/i&gt;-protected amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000126</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>G. R.</given-names></name>
<name><surname>Cohen</surname>
<given-names>D.</given-names></name>
<name><surname>Pattenden</surname>
<given-names>G. E.</given-names></name>
<name><surname>Thomas</surname>
<given-names>J. A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>126</fpage>
<lpage>128</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000126">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000126">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and biosynthesis. Part XII. Stereochemical studies related to the biosynthesis of the morphine alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Bhakuni</surname>
<given-names>D. S.</given-names></name>
<name><surname>James</surname>
<given-names>R.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>128</fpage>
<lpage>132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intermediates and dyestuffs for synthetic fibres. Part I. Arylaminonitropyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000132</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>M. G. W.</given-names></name>
<name><surname>Day</surname>
<given-names>M.</given-names></name>
<name><surname>Peters</surname>
<given-names>A. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>132</fpage>
<lpage>136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000132">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000132">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Configurational inversion in the hydrogenolysis of benzyl alcohol derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khan</surname>
<given-names>A. M.</given-names></name>
<name><surname>McQuillin</surname>
<given-names>F. J.</given-names></name>
<name><surname>Jardine</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>136</fpage>
<lpage>139</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 tetralones and their enamines with cyanogen halides: a new synthesis of 2-naphthylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000140</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parfitt</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>140</fpage>
<lpage>142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000140">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000140">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclic photoproduct from phorone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000143</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kropp</surname>
<given-names>P. J.</given-names></name>
<name><surname>Gibson</surname>
<given-names>T. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>143</fpage>
<lpage>145</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000143">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000143">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sneezewood, &lt;i&gt;Ptaeroxylon obliquum&lt;/i&gt;(Thunb.) Radlk. Part I. Chromones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000145</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McCabe</surname>
<given-names>P. H.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>145</fpage>
<lpage>151</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000145">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000145">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 studies related to franklinone and acid-catalysed rearrangements of pyronochromanone derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000151</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jefferson</surname>
<given-names>A.</given-names></name>
<name><surname>Moore</surname>
<given-names>I.</given-names></name>
<name><surname>Scheinmann</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>151</fpage>
<lpage>154</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000151">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000151">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 from croton species. Part VI. Mass spectrometric studies of the crotonosine alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000154</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>M.</given-names></name>
<name><surname>Loudon</surname>
<given-names>A. G.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
<name><surname>Stuart</surname>
<given-names>K. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>154</fpage>
<lpage>161</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000154">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000154">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 studies. Part V. The synthesis of Taiwanin A</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000161</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swoboda</surname>
<given-names>Gertrude A.</given-names></name>
<name><surname>Wang</surname>
<given-names>Kung-Tsung</given-names></name>
<name><surname>Weinstein</surname>
<given-names>Boris</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>161</fpage>
<lpage>162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000161">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000161">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>West African timbers. Part XIX. The structure of methyl angolensate, a ring-B-seco tetranor-tetracyclic triterpene of the meliacin family</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
<name><surname>Powell</surname>
<given-names>J. W.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Toft</surname>
<given-names>P.</given-names></name>
<name><surname>Welford</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>163</fpage>
<lpage>170</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;Cedrela odorata&lt;/i&gt; L. The structure of methyl angolensate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000171</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Magnus</surname>
<given-names>K. E.</given-names></name>
<name><surname>Mootoo</surname>
<given-names>B. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>171</fpage>
<lpage>177</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 orientation of the alkyl groups of the end rings of natural and racemic stercobilin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000178</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>C. H.</given-names></name>
<name><surname>Lemmon</surname>
<given-names>Gillian A.</given-names></name>
<name><surname>Nicholson</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>178</fpage>
<lpage>181</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000178">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000178">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The nuclear magnetic resonances of angular methyl groups in steroid ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000181</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cherry</surname>
<given-names>P. C.</given-names></name>
<name><surname>Cottrell</surname>
<given-names>W. R. T.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Richards</surname>
<given-names>(Mrs.) E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>181</fpage>
<lpage>184</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000181">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000181">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Syntheses of hexa-3,4-dien-1-ol and penta-2,3-dien-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000185</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landor</surname>
<given-names>Phyllis D.</given-names></name>
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Pepper</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>185</fpage>
<lpage>189</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000185">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000185">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. The synthesis of allenynols and allenenols by the reduction of 4,6-diyn-2-en-1-ols and diynediols with lithium aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000189</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Pepper</surname>
<given-names>E. S.</given-names></name>
<name><surname>Regan</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>189</fpage>
<lpage>193</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000189">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000189">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. The addition of dihalocarbenes to allenes and conversion of 1,1-dihalo-2-methylenecyclopropanes to cumulenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000194</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ball</surname>
<given-names>W. J.</given-names></name>
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Punja</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>194</fpage>
<lpage>197</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000194">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000194">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 synthesis. Part III. The reduction of ketones with the ethanol modified lithium aluminium hydride-3-&lt;i&gt;O&lt;/i&gt;-benzyl-1,2-&lt;i&gt;O&lt;/i&gt;-cyclohexylidene-α-D-glucofuranose complex</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000197</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>197</fpage>
<lpage>201</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000197">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000197">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 derivatives of 6-aminofulvene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000201</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Childs</surname>
<given-names>R. F.</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>201</fpage>
<lpage>210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000201">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000201">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 acetylation of aluminium(III) and iron(III) acetyl-acetonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000211</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Doolan</surname>
<given-names>P. C.</given-names></name>
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>211</fpage>
<lpage>213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LV. Pyridobenzacridines and related heterocycles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>213</fpage>
<lpage>215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 3-acetoxycholesta-1,3-diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000215</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellamy</surname>
<given-names>A. J.</given-names></name>
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>215</fpage>
<lpage>215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000215">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000215">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvolysis of the trichloroacetate of &lt;i&gt;endo&lt;/i&gt;-bicyclo[3,1,0]hex-2-en-6-yl-methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000216</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lumb</surname>
<given-names>J. T.</given-names></name>
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>216</fpage>
<lpage>218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000216">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000216">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phytotoxic compounds produced by &lt;i&gt;Fusarium equiseti&lt;/i&gt;. Part III. Nuclear magnetic resonance spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000218</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tidd</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>218</fpage>
<lpage>220</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000218">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000218">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part XL. Protected derivatives of the tri- and tetra-peptides of alanine and serine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000221</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
<name><surname>Sparrow</surname>
<given-names>D. R.</given-names></name>
<name><surname>Beacham</surname>
<given-names>J.</given-names></name>
<name><surname>Ivanov</surname>
<given-names>V. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>221</fpage>
<lpage>226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000221">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000221">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamines. Part II. The reaction of enamines with methyl vinyl ketone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000226</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>Ian</given-names></name>
<name><surname>Karger</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>226</fpage>
<lpage>235</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000226">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000226">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Migration of double bonds in end-blocked linear olefinic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000235</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>235</fpage>
<lpage>238</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 solvolysis of arylidene-1-methyl-1&lt;i&gt;H&lt;/i&gt;-tetrazol-5-yl-hydrazidic bromides: a route to 6-aryl-3-methyl[1,2,4]triazolo[4,3-&lt;i&gt;d&lt;/i&gt;]-tetrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000239</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>R. N.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>239</fpage>
<lpage>244</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000239">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000239">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 Grignard reagents with &lt;i&gt;N&lt;/i&gt;-substituted maleimides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000245</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Queen</surname>
<given-names>A.</given-names></name>
<name><surname>Reipas</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>245</fpage>
<lpage>246</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 isolation of cycloartenol and 24-methylenecycloartanol from false kola nuts (&lt;i&gt;Garcinia kola&lt;/i&gt; Heckel)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000246</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Blasdale</surname>
<given-names>J. H. C.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Hornby</surname>
<given-names>G. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>246</fpage>
<lpage>248</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000246">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000246">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some 3-deoxy-D-ribofuranose derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000249</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>249</fpage>
<lpage>252</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 syntheses of halogeno- and deoxy-sugars</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000252</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>252</fpage>
<lpage>256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000252">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000252">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 removal of toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl groups from sulphonamides. Part III. Some &lt;i&gt;N&lt;/i&gt;-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl glycine esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000256</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hannah</surname>
<given-names>E. D.</given-names></name>
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
<name><surname>Rehman</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>256</fpage>
<lpage>261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000256">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000256">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 santonin. Part VIII. Interconversion of the desmotroposantonins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolt</surname>
<given-names>A. J. N.</given-names></name>
<name><surname>Garson</surname>
<given-names>Miss M. S.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>L. O.</given-names></name>
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Nisbet</surname>
<given-names>M. A.</given-names></name>
<name><surname>Shaw</surname>
<given-names>S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>261</fpage>
<lpage>270</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 catalytic hydrogenation of unsaturated aldehydes to form saturated aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000270</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jardine</surname>
<given-names>F. H.</given-names></name>
<name><surname>Wilkinson</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>270</fpage>
<lpage>271</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000270">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000270">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biphenylenes. Part XVI. Preparation and Baeyer–Villiger oxidation of some 2-acetylbiphenylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blatchly</surname>
<given-names>J. M.</given-names></name>
<name><surname>Gardner</surname>
<given-names>D. V.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>272</fpage>
<lpage>274</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvolytic rearrangements of bicyclo[3,2,0]hept-6-en-2-yl and bicyclo-[3,2,0]hept-2-yl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000274</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>S. C.</given-names></name>
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>274</fpage>
<lpage>281</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000274">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000274">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lindcarpine, an alkaloid from &lt;i&gt;Lindera pipericarpa&lt;/i&gt; Boerl (Lauraceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiang</surname>
<given-names>A. K.</given-names></name>
<name><surname>Sim</surname>
<given-names>K. Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>282</fpage>
<lpage>283</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Rhizophoraceae&lt;/i&gt; alkaloids. Part I. Four sulphur-containing bases from &lt;i&gt;Cassipourea&lt;/i&gt; spp.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000283</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wright</surname>
<given-names>Winifred G.</given-names></name>
<name><surname>Warren</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>283</fpage>
<lpage>284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000283">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000283">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Rhizophoraceae&lt;/i&gt; alkaloids. Part II. Gerrardine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000284</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wright</surname>
<given-names>Winifred G.</given-names></name>
<name><surname>Warren</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>284</fpage>
<lpage>285</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000284">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000284">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Rhizophoraceae&lt;/i&gt; alkaloids. Part III. Cassipourine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000286</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Warren</surname>
<given-names>F. L.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>286</fpage>
<lpage>288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000286">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000286">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-aminoetetralin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000288</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thrift</surname>
<given-names>R. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>288</fpage>
<lpage>293</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000288">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000288">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 analogues of pharmacologically active compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000293</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>Pinder</surname>
<given-names>R. M.</given-names></name>
<name><surname>Sawhney</surname>
<given-names>S. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>293</fpage>
<lpage>296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000293">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000293">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1-substituted 5-hydroxy-2-phenylindole derivatives from quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000296</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Betkerur</surname>
<given-names>S. N.</given-names></name>
<name><surname>Siddappa</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>296</fpage>
<lpage>298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000296">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000296">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The preparation of compounds of the composition R&lt;sub&gt;2&lt;/sub&gt;Sn(OMe)X</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000298</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>298</fpage>
<lpage>300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diterpenes from the volatile oil of &lt;i&gt;Dacrydium colensoi&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000300</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>R. E.</given-names></name>
<name><surname>Smith</surname>
<given-names>R. A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>300</fpage>
<lpage>302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000300">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000300">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and mass spectra of some aryl-alkyl sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Entwistle</surname>
<given-names>I. D.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>302</fpage>
<lpage>306</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 mass spectra of organic compounds. Part II. Some 1,2-oxaza-ring systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000307</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
<name><surname>Wise</surname>
<given-names>E. J.</given-names></name>
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>307</fpage>
<lpage>309</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000307">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000307">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Methoxy-3-methylbenzofurano-4,7-quinone; dimers of 3-methylbenzofurans; and tautomerism in 2-acetyl-3-hydroxy-5-methoxy-1,4-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000310</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cavell</surname>
<given-names>B. D.</given-names></name>
<name><surname>MacMillan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>310</fpage>
<lpage>313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000310">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000310">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and bromination of some cyclic sulphites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bristow</surname>
<given-names>P. A.</given-names></name>
<name><surname>Jones</surname>
<given-names>R. G.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>314</fpage>
<lpage>315</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. Preparative routes to indoles with t-amine substituents in the benzene ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000315</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainsworth</surname>
<given-names>D. P.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>315</fpage>
<lpage>319</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000315">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000315">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 fluorine compounds. Part XXXVI. Preparation of &lt;i&gt;N&lt;/i&gt;-substituted amides of α-fluoroacids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000319</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shahak</surname>
<given-names>Israel</given-names></name>
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>319</fpage>
<lpage>320</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000319">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000319">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 synthesis of hydroxy-1,2,3-benzothiadiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000321</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>J. H.</given-names></name>
<name><surname>Kirby</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>321</fpage>
<lpage>323</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000321">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000321">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2-substituted-4-phenacylidenehomophthalimides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Ledger</surname>
<given-names>A. P.</given-names></name>
<name><surname>Perkins</surname>
<given-names>N. R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>323</fpage>
<lpage>326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 use of phenylsodium in the preparation of alkylpyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000326</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grzeskowiak</surname>
<given-names>R.</given-names></name>
<name><surname>Jeffery</surname>
<given-names>G. H.</given-names></name>
<name><surname>Watling</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>326</fpage>
<lpage>327</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000326">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000326">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 biphenyl-2,2′-dialdehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000328</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Bracha</surname>
<given-names>Perez</given-names></name>
<name><surname>Agranat</surname>
<given-names>Israel</given-names></name>
<name><surname>Kraus</surname>
<given-names>Menahem A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>328</fpage>
<lpage>329</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000328">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000328">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Minor alkaloids of &lt;i&gt;Heliotropium indicum&lt;/i&gt; L</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mattocks</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>329</fpage>
<lpage>331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 origin of naturally-occurring acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000332</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bu'Lock</surname>
<given-names>J. D.</given-names></name>
<name><surname>Smith</surname>
<given-names>G. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>332</fpage>
<lpage>336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 chagi</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000336</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bu'Lock</surname>
<given-names>J. D.</given-names></name>
<name><surname>Walker</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>336</fpage>
<lpage>338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000336">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000336">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVIII. The structure of digacetigenin: comparative experiments with ruscogenin and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Lack</surname>
<given-names>Ruth E.</given-names></name>
<name><surname>Newman</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>339</fpage>
<lpage>343</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>β-Aroylpropionic acids. Part XXI. The Fries rearrangement of chlorophenyl hydrogen succinates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000343</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Enayat (Mrs.) </surname>
<given-names>I.</given-names></name>
<name><surname>Abdel-Wahab</surname>
<given-names>S. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>343</fpage>
<lpage>346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000343">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000343">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of (±)-2-acetamido-2,5-dihydro-5-oxofuran from &lt;i&gt;Fusarium equiseti&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>White</surname>
<given-names>E. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>346</fpage>
<lpage>347</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bridged ring systems. Part XII. The stereoselective synthesis of &lt;i&gt;meso&lt;/i&gt;-&lt;i&gt;trans&lt;/i&gt;-2-carboxymethyl-1,3-dimethylcyclohexane-1,3-dicarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000348</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>J.</given-names></name>
<name><surname>Parker</surname>
<given-names>W.</given-names></name>
<name><surname>Raphael</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>348</fpage>
<lpage>357</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000348">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000348">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some dihalogenocyclopropanes into unsaturated ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000358</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Iskander</surname>
<given-names>G. M.</given-names></name>
<name><surname>Magboul</surname>
<given-names>B. I.</given-names></name>
<name><surname>Stansfield</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>358</fpage>
<lpage>361</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000358">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000358">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 garryfoline–cuauchichicine rearrangement: a study of the mechanism in the (–)-kaurenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000361</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnes</surname>
<given-names>M. F.</given-names></name>
<name><surname>MacMillan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>361</fpage>
<lpage>366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000361">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000361">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and 1,4-benzodiazepines. Part XXXII. The acetic anhydride rearrangement of 1,4-benzodiazepinones to isoindoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000366</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fryer</surname>
<given-names>R. Ian</given-names></name>
<name><surname>Brust</surname>
<given-names>B.</given-names></name>
<name><surname>Earley</surname>
<given-names>J. V.</given-names></name>
<name><surname>Sternbach</surname>
<given-names>L. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>366</fpage>
<lpage>367</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000366">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000366">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oligomers of allene. Part II. Dimers and trimers formed in the thermal polymerisation of liquid allene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Weinstein</surname>
<given-names>B.</given-names></name>
<name><surname>Fenselau</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>368</fpage>
<lpage>372</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000368">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 in the solvolysis of some carbohydrate nitrobenzene-&lt;i&gt;p&lt;/i&gt;-sulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000372</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Austin</surname>
<given-names>P. W.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Saunders</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>372</fpage>
<lpage>377</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000372">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000372">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Tetrahydro- and decahydro-1,5-, -1,6-, -1,7-, and -1,8-naphthyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000377</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>377</fpage>
<lpage>383</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000377">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000377">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Liquid-phase photolysis. Part X. Formation of spiro-oxetans by photoaddition of olefins to &lt;i&gt;p&lt;/i&gt;-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000383</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryce-Smith</surname>
<given-names>D.</given-names></name>
<name><surname>Gilbert</surname>
<given-names>A.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>383</fpage>
<lpage>389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000383">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000383">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Liquid-phase photolysis. Part XI. Stereochemistry of the photoaddition of maleic anhydride to benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000390</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryce-Smith</surname>
<given-names>D.</given-names></name>
<name><surname>Vickery</surname>
<given-names>B.</given-names></name>
<name><surname>Fray</surname>
<given-names>G. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>390</fpage>
<lpage>394</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000390">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000390">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The preparation and properties of A-homo-5α-cholestan-4-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000394</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Morris</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>394</fpage>
<lpage>396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000394">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000394">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pharmacodynamic compounds. Part V. Some derivatives of monocrotaline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Constantine</surname>
<given-names>M. F.</given-names></name>
<name><surname>Mehta</surname>
<given-names>M. D.</given-names></name>
<name><surname>Ward</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>397</fpage>
<lpage>399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 halogenated amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000400</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Godfrey</surname>
<given-names>K. E.</given-names></name>
<name><surname>Thrift</surname>
<given-names>R. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>400</fpage>
<lpage>404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000400">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000400">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Involutin, a diphenylcyclopenteneone from &lt;i&gt;Paxillus involutus&lt;/i&gt;(Oeder ex Fries)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
<name><surname>Elsworthy</surname>
<given-names>G. C.</given-names></name>
<name><surname>Kale</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>405</fpage>
<lpage>409</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The phenolic constituents of &lt;i&gt;Boletus&lt;/i&gt;(&lt;i&gt;Leccinum&lt;/i&gt;)&lt;i&gt;scaber&lt;/i&gt;(Bull ex Fr.) Gray</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
<name><surname>Elsworthy</surname>
<given-names>G. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>410</fpage>
<lpage>411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Some analogues of hispidin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
<name><surname>Mir</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>411</fpage>
<lpage>413</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The photodimerisation of hispidin analogues; a proton magnetic resonance study</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000413</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartle</surname>
<given-names>K. D.</given-names></name>
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. W.</given-names></name>
<name><surname>Mir</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>413</fpage>
<lpage>419</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000413">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000413">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 seven-membered ring derivatives. Part VI. Conformation of (+)-6β-bromo-3,8-dimethyldecahydrozaulen-5-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kuriyama</surname>
<given-names>K.</given-names></name>
<name><surname>Iwata</surname>
<given-names>T.</given-names></name>
<name><surname>Moriyama</surname>
<given-names>M.</given-names></name>
<name><surname>Ishikawa</surname>
<given-names>M.</given-names></name>
<name><surname>Minato</surname>
<given-names>H.</given-names></name>
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>420</fpage>
<lpage>423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sesquiterpenoids. Part XV. Structure and absolute configuration of oplodiol, a new sesquiterpene alcohol from &lt;i&gt;Oplopanax japonicus&lt;/i&gt;(Nakai) Nakai</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000423</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Minato</surname>
<given-names>Hitoshi</given-names></name>
<name><surname>Ishikawa</surname>
<given-names>Makoto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>423</fpage>
<lpage>427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000423">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000423">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;-fluoro-compounds. Part II. Reaction of perfluoro-&lt;i&gt;N&lt;/i&gt;-fluoropiperidine or perfluoro-&lt;i&gt;N&lt;/i&gt;-fluoromorpholine with manganese pentacarbonyl hydride to give the corresponding &lt;i&gt;N&lt;/i&gt;–H compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000427</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>Hatton</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>427</fpage>
<lpage>430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000427">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000427">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 unsymmetrical diglycerides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gigg</surname>
<given-names>Jill</given-names></name>
<name><surname>Gigg</surname>
<given-names>Roy</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>431</fpage>
<lpage>434</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 related to northebaine. Part II. Derivatives of nororipavine and 8,14-dihydronororipavine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000434</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartels-Keith</surname>
<given-names>J. R.</given-names></name>
<name><surname>Hills</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>434</fpage>
<lpage>440</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000434">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000434">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 β,&lt;i&gt;γ&lt;/i&gt;-unsaturated lactone C&lt;sub&gt;31&lt;/sub&gt;H&lt;sub&gt;44&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt; obtained by oxidation of methyl oleana-11,13(18)-dien-28-oate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000441</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eade</surname>
<given-names>R. A.</given-names></name>
<name><surname>Kornis</surname>
<given-names>G.</given-names></name>
<name><surname>Simes</surname>
<given-names>J. J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>441</fpage>
<lpage>441</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000441">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000441">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;i&gt;S&lt;/i&gt;-β-D-glucopyranosyl-6-thio-D-glucopyranose. A thioglycosidic analogue of gentiobiose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000442</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hutson</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>442</fpage>
<lpage>444</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000442">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000442">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 isolation and structure of papaverrubine C (epiporphyroxine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000444</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hughes</surname>
<given-names>D. W.</given-names></name>
<name><surname>Kühn</surname>
<given-names>L.</given-names></name>
<name><surname>Pfeifer</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>444</fpage>
<lpage>446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000444">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000444">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 choline phosphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000447</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bird</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>447</fpage>
<lpage>447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000447">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000447">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Taxine. Part V. The structure of taxicin-II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000448</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dukes</surname>
<given-names>M.</given-names></name>
<name><surname>Eyre</surname>
<given-names>D. H.</given-names></name>
<name><surname>Harrison</surname>
<given-names>J. W.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>448</fpage>
<lpage>452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000448">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000448">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Taxine. Part VI. The stereochemistry of taxicin-I and taxicin-II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eyre</surname>
<given-names>D. H.</given-names></name>
<name><surname>Harrison</surname>
<given-names>J. W.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>452</fpage>
<lpage>462</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The synthesis of pyrido[1,2-&lt;i&gt;a&lt;/i&gt;]thiazolo[2,3-&lt;i&gt;c&lt;/i&gt;]pyrazidi-inium and pyrido[1,2-&lt;i&gt;a&lt;/i&gt;]thiazolo-[4,3-&lt;i&gt;c&lt;/i&gt;]pyrazidi-inium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glover</surname>
<given-names>E. E.</given-names></name>
<name><surname>Thomas</surname>
<given-names>T. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>463</fpage>
<lpage>466</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nucleophilic reactions of cyanuric chloride and of certain 2,4-dichloro-1,3,5-triazines with compounds containing reactive hydrogen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000466</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beech</surname>
<given-names>W. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>466</fpage>
<lpage>472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000466">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000466">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclopropanones and related compounds. Part II. Adducts from reduction of di-(α-bromobenzyl) ketone in the presence of dienes. Photolysis of α-phenyl ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000473</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Nye</surname>
<given-names>M. J.</given-names></name>
<name><surname>Subrahmanyam</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>473</fpage>
<lpage>479</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000473">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000473">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 macrocyclic glycolipids from &lt;i&gt;Torulopsis gropengiesseri&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000479</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>479</fpage>
<lpage>484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000479">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000479">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Oxidative hydroboronation of car-2-, -3-, and -4-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000485</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
<name><surname>Staniland</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>485</fpage>
<lpage>489</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000485">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000485">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triterpenes from &lt;i&gt;Salvia glutinosa&lt;/i&gt; L.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000490</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>490</fpage>
<lpage>490</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000490">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000490">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Base-catalysed reactions of glyoxal. Part I. 1,4-Diformyl- and 1,4-bis-methylsulphonyl- derivatives of 2,3,5,6-tetrahydroxypiperazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000491</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Currie</surname>
<given-names>A. C.</given-names></name>
<name><surname>Dinwoodie</surname>
<given-names>A. H.</given-names></name>
<name><surname>Fort</surname>
<given-names>G.</given-names></name>
<name><surname>Thompson</surname>
<given-names>J. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>491</fpage>
<lpage>496</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000491">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000491">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Base-catalysed reactions of glyoxal. Part II. 2,3,5,6-Tetrahydroxypiperazine-1,4-disulphonic acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000496</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dinwoodie</surname>
<given-names>A. H.</given-names></name>
<name><surname>Gibson</surname>
<given-names>J. A.</given-names></name>
<name><surname>Parker</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>496</fpage>
<lpage>497</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000496">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000496">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bicyclic pyrimidine derivatives with a bridgehead nitrogen atom. Part I. Synthesis of &lt;i&gt;s&lt;/i&gt;-triazolo[4,3-&lt;i&gt;a&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000498</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spickett</surname>
<given-names>R. G. W.</given-names></name>
<name><surname>Wright</surname>
<given-names>S. H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>498</fpage>
<lpage>502</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000498">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000498">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bicyclic pyrimidine derivatives with a bridgehead nitrogen atom. Part II. Synthesis of &lt;i&gt;s&lt;/i&gt;-triazolo[1,5-&lt;i&gt;a&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000503</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spickett</surname>
<given-names>R. G. W.</given-names></name>
<name><surname>Wright</surname>
<given-names>S. H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>503</fpage>
<lpage>506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000503">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000503">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Phenylnaphthalene. Part VI. Action of Grignard reagents on 1-phenyl- and 7-methoxy-1-&lt;i&gt;p&lt;/i&gt;-methoxyphenyl-2,3-naphthalene-dicarboxylic anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Sherif</surname>
<given-names>Sayed</given-names></name>
<name><surname>Ekladios</surname>
<given-names>Labib</given-names></name>
<name><surname>Azab</surname>
<given-names>Abed El-Aziz</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>506</fpage>
<lpage>509</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 rose-bay willow-herb</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000510</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glen</surname>
<given-names>A. T.</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>Younes</surname>
<given-names>M. El-Garby</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>510</fpage>
<lpage>515</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000510">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000510">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thiazolopyridinium salts. Part I. Synthesis of some thiazolo[3,2-&lt;i&gt;a&lt;/i&gt;]-pyridinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000515</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
<name><surname>Jones</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>515</fpage>
<lpage>518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbohydrate derivatives of 1-substituted 1,2,3-triazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Shaban</surname>
<given-names>M. A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>519</fpage>
<lpage>520</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Automatic detection of structural similarities among chemical compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000521</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armitage</surname>
<given-names>Janet E.</given-names></name>
<name><surname>Lynch</surname>
<given-names>Michael F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>521</fpage>
<lpage>528</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000521">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000521">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;NN&lt;/i&gt;-dimethyl-2-fluoro-2-phenylethylamine: preparation and solvolysis in aqueous acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000528</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
<name><surname>Westwood</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>528</fpage>
<lpage>530</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000528">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000528">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 total synthesis of (±)-scoulerine and (±)-tetrahydropalmatine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000530</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>530</fpage>
<lpage>532</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000530">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000530">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroidal sulphur compounds. Part I. Pyrolysis and absolute configuration of steroidal phenyl sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000532</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. Neville</given-names></name>
<name><surname>Green</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>532</fpage>
<lpage>542</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000532">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000532">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 œstrogen monoglucuronides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000542</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elce</surname>
<given-names>J. S.</given-names></name>
<name><surname>Carpenter</surname>
<given-names>J. G. D.</given-names></name>
<name><surname>Kellie</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>542</fpage>
<lpage>550</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000542">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000542">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 solvolysis of gibberellin A&lt;sub&gt;5&lt;/sub&gt; methyl ester toluene-&lt;i&gt;p&lt;/i&gt;-sulphonate — a bicyclo[3,2,1]octane bridgehead derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000550</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>550</fpage>
<lpage>554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the seed of &lt;i&gt;Khaya senegalensis&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adesogan</surname>
<given-names>E. K.</given-names></name>
<name><surname>Powell</surname>
<given-names>J. W.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>554</fpage>
<lpage>556</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 high-boiling petroleum distillates. Part X. 1,2,7,8-Tetramethylfluorene and methylbenzo[&lt;i&gt;a&lt;/i&gt;]fluorenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000556</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
<name><surname>Stewart</surname>
<given-names>H. N. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>556</fpage>
<lpage>560</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000556">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000556">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 high-boiling petroleum distillates. Part XI. Methyl homologues of chrysene and 11-thiabenzo[&lt;i&gt;a&lt;/i&gt;]fluorene in a Kuwait oil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000560</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
<name><surname>Stewart</surname>
<given-names>H. N. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>560</fpage>
<lpage>562</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitramines. Part IV. Preparation and nitrolysis of the condensation products of ethylenedinitramine with formaldehyde and some diamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000562</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>J. A.</given-names></name>
<name><surname>Dunstan</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>562</fpage>
<lpage>565</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000562">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000562">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 macrocylic compounds. Part XLIV. Studies in the hydroanthracene series. The synthesis of 3,4-benzocyclodeca-3,8-diene-1,6-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garratt</surname>
<given-names>P. J.</given-names></name>
<name><surname>Sondheimer</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>565</fpage>
<lpage>568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The formation and reactivity of 2-, 4-, and 5-pyrimidinyl sulphones and sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000568</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Ford</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>568</fpage>
<lpage>572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000568">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000568">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. 5-Nitropyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000573</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biffin</surname>
<given-names>M. E. C.</given-names></name>
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Lee</surname>
<given-names>T. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>573</fpage>
<lpage>574</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000573">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000573">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 3,12,15-trimethyldocosanoate and 3,15-dimethyldocosanoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000575</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Minnikin</surname>
<given-names>D. E.</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>575</fpage>
<lpage>577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000575">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000575">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thiophens. Part III. Synthesis of thienyl- and furyl-acetylene derivatives from cuprous acetylides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000578</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. E.</given-names></name>
<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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>578</fpage>
<lpage>582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000578">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000578">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-steroids. Part II. 6-Amino-androstanes and -pregnanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000582</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewett</surname>
<given-names>C. L.</given-names></name>
<name><surname>Savage</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>582</fpage>
<lpage>588</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000582">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000582">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 laurate esters of pyrogallol and related phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000588</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duuren</surname>
<given-names>B. L. Van</given-names></name>
<name><surname>Conklin</surname>
<given-names>M.</given-names></name>
<name><surname>Lavers</surname>
<given-names>G. C.</given-names></name>
<name><surname>Segal</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>588</fpage>
<lpage>590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000588">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000588">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 7,12-dihydro-8,9-benzopleiadene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000591</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Houlton</surname>
<given-names>P. R.</given-names></name>
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>591</fpage>
<lpage>591</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000591">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000591">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyto-active amino-acids and peptides. Part XII. Derivatives of serine and tyrosine and related hydroxy compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000592</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wade</surname>
<given-names>Roy</given-names></name>
<name><surname>Bergel</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>592</fpage>
<lpage>595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000592">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000592">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXV. The mechanism of the base-catalysed racemisation of the &lt;i&gt;p&lt;/i&gt;-nitrophenyl esters of acylpeptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000595</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Antonovics</surname>
<given-names>(Miss) I.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>595</fpage>
<lpage>601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of tropolones. Part III. The photo-oxidation of tetra-&lt;i&gt;O&lt;/i&gt;-methylpurpurogallin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000601</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>E. J.</given-names></name>
<name><surname>Griffiths</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>601</fpage>
<lpage>604</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000601">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000601">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peucenin from sneezewood (&lt;i&gt;Ptaeroxylon obliquum&lt;/i&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000604</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pachler</surname>
<given-names>K. G. R.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>604</fpage>
<lpage>606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000604">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000604">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 analogous to the &lt;i&gt;N&lt;/i&gt;-terminal eicosapeptide of ribonuclease A. Part IV. Synthesis of the enzymatically active Orn&lt;sup&gt;10&lt;/sup&gt; and Orn&lt;sup&gt;10&lt;/sup&gt;, Glu&lt;sup&gt;11&lt;/sup&gt;-eicosapeptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000606</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scoffone</surname>
<given-names>Ernesto</given-names></name>
<name><surname>Rocchi</surname>
<given-names>Raniero</given-names></name>
<name><surname>Marchiori</surname>
<given-names>Fernando</given-names></name>
<name><surname>Marzotto</surname>
<given-names>Armando</given-names></name>
<name><surname>Scatturin</surname>
<given-names>Angelo</given-names></name>
<name><surname>Tamburro</surname>
<given-names>Antonmario</given-names></name>
<name><surname>Vidali</surname>
<given-names>Giorgio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>606</fpage>
<lpage>610</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000606">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000606">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydroxyquinones. Part II. The autoxidation of 3,6-dimethylbenzene-1,2,4-triol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000611</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>John F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>611</fpage>
<lpage>620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000611">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000611">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinolizidines. Part IV. The cyclopenta[&lt;i&gt;ij&lt;/i&gt;]quinolizidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Wells</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>621</fpage>
<lpage>626</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinolizidines. Part V. The stereochemistry of the oxoquinolizidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000626</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mason</surname>
<given-names>S. F.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Wells</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>626</fpage>
<lpage>631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000626">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000626">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. The structure of isolinderoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
<name><surname>Minato</surname>
<given-names>H.</given-names></name>
<name><surname>Horibe</surname>
<given-names>I.</given-names></name>
<name><surname>Miyawaki</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>631</fpage>
<lpage>634</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 structure of sporidesmolide IV, a cyclohexadepsipeptide from &lt;i&gt;Pithomyces maydicus&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000634</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bishop</surname>
<given-names>(Mrs.) Elizabeth</given-names></name>
<name><surname>Russell</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>634</fpage>
<lpage>638</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000634">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000634">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Dithians. Part I. Ring contractions in the 1,3-dithian series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>E.</given-names></name>
<name><surname>Beer</surname>
<given-names>R. J. S.</given-names></name>
<name><surname>Harris</surname>
<given-names>D.</given-names></name>
<name><surname>Royall</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>638</fpage>
<lpage>643</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the methyl 1-deoxy-1-mercapto-D-ribosides and the hydrolysis of methyl 1-deoxy-1-mercapto-α-D-ribopyranoside</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000644</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clayton</surname>
<given-names>C. J.</given-names></name>
<name><surname>Hughes</surname>
<given-names>N. A.</given-names></name>
<name><surname>Saeed</surname>
<given-names>S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>644</fpage>
<lpage>648</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000644">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000644">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 partial synthesis of aldosterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000648</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nagata</surname>
<given-names>Wataru</given-names></name>
<name><surname>Narisada</surname>
<given-names>Masayuki</given-names></name>
<name><surname>Sugasawa</surname>
<given-names>Tsutomu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>648</fpage>
<lpage>660</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. 1,2,4-Triazole-3-sulphonic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000661</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackman</surname>
<given-names>A. J.</given-names></name>
<name><surname>Browne</surname>
<given-names>E. J.</given-names></name>
<name><surname>Polya</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>661</fpage>
<lpage>662</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000661">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000661">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LVI. Benz[&lt;i&gt;c&lt;/i&gt;]acridines and benzo[&lt;i&gt;a&lt;/i&gt;]carbazoles methylated on the K-zone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000662</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Mangane</surname>
<given-names>M.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>662</fpage>
<lpage>665</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000662">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000662">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LVII. Hexacyclic acridines derived from phenanthrene and fluorene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000665</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thang</surname>
<given-names>D. C.</given-names></name>
<name><surname>Weisburger</surname>
<given-names>(Mrs.) Elizabeth K.</given-names></name>
<name><surname>Mabille</surname>
<given-names>Ph.</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>665</fpage>
<lpage>668</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000665">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000665">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;Erythroxylon monogynum&lt;/i&gt; Roxb. Part III. Erythroxytriols P and Q</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000668</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connolly</surname>
<given-names>J. D.</given-names></name>
<name><surname>Gunn</surname>
<given-names>D. M.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. D. H.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>668</fpage>
<lpage>674</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000668">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000668">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 products of &lt;i&gt;NN&lt;/i&gt;-dimethyl-&lt;i&gt;p&lt;/i&gt;-phenylazoaniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000674</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Douglas</surname>
<given-names>A. F.</given-names></name>
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Hooper</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>674</fpage>
<lpage>680</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000674">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000674">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phenylmagnesium bromide with 2-benzoyl-1-indanone and its enol methyl ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000680</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Auld</surname>
<given-names>D.</given-names></name>
<name><surname>Heller</surname>
<given-names>H. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>680</fpage>
<lpage>681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000680">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000680">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Overcrowded molecules. Part I. 1,2-Bisdiphenylmethyleneindane and 1,2-bisdiphenylmethylene-3,3-dimethylindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000682</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heller</surname>
<given-names>H. G.</given-names></name>
<name><surname>Auld</surname>
<given-names>D.</given-names></name>
<name><surname>Salisbury</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>682</fpage>
<lpage>685</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000682">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000682">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 gas-phase reactions of sulphur with amines and related compounds: a novel synthesis of thaizoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000685</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Colebourne</surname>
<given-names>N.</given-names></name>
<name><surname>Foster</surname>
<given-names>R. G.</given-names></name>
<name><surname>Robson</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>685</fpage>
<lpage>688</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000685">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000685">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 activated esters of &lt;i&gt;N&lt;/i&gt;-protected amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000689</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wolman</surname>
<given-names>Y.</given-names></name>
<name><surname>Ladkany</surname>
<given-names>D.</given-names></name>
<name><surname>Frankel</surname>
<given-names>Max</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>689</fpage>
<lpage>690</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000689">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000689">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amide hydrazones from hydrazones and sulphonyl chloride–amide complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000690</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hoyle</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>690</fpage>
<lpage>693</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000690">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000690">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pyrrolo[3,4-&lt;i&gt;d&lt;/i&gt;]pyrimidines: their preparation from 3-amino-4-cyano-3-pyrrolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000693</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cavalla</surname>
<given-names>J. F.</given-names></name>
<name><surname>Willis</surname>
<given-names>J. A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>693</fpage>
<lpage>697</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000693">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000693">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Amino-4-thiocarbamoyl-3-pyrrolines: their conversion into pyrrolo[3,4-&lt;i&gt;d&lt;/i&gt;]pyrimidine-4-thiols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000698</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cavalla</surname>
<given-names>J. F.</given-names></name>
<name><surname>Webb</surname>
<given-names>N. E.</given-names></name>
<name><surname>Willis</surname>
<given-names>J. A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>698</fpage>
<lpage>701</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000698">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000698">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sulphonylureas</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000701</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tull</surname>
<given-names>Roger</given-names></name>
<name><surname>O'Neill</surname>
<given-names>Robert C.</given-names></name>
<name><surname>McCarthy</surname>
<given-names>Edmund P.</given-names></name>
<name><surname>Pappas</surname>
<given-names>James J.</given-names></name>
<name><surname>Chemerda</surname>
<given-names>John M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>701</fpage>
<lpage>702</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000701">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000701">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-isomerisation of 1-(2,4-dimethoxyphenyl)but-2-en-1-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000702</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>702</fpage>
<lpage>703</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000702">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000702">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Colouring matters of the Aphididae. Part XXXII. Rhodoaphin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000704</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>704</fpage>
<lpage>707</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000704">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000704">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Colouring matters of the Aphididae. Part XXXIII. &lt;i&gt;Dactynaphins&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000708</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>708</fpage>
<lpage>711</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000708">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000708">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Colouring matters of the Aphididae. Part XXXIV. Rhodo- and xantho-dactynaphins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>712</fpage>
<lpage>720</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Colouring matters of the Aphididae. Part XXXV. Protodactynaphin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000720</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>720</fpage>
<lpage>723</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000720">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000720">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. A dipheno-2,2′-quinone from 2,2′-dihydroxy-5,5′-dimethoxy-4,4′-di-t-butylbiphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000723</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
<name><surname>Hewitt</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>723</fpage>
<lpage>725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000723">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000723">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The reaction of 2,2′-dihydroxy-5,5′-dimethoxy-3,3′-di-t-butylbiphenyl with lead tetra-acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
<name><surname>Hewitt</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>726</fpage>
<lpage>730</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000726">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. 2-Substituted compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000731</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>Saraf</surname>
<given-names>S. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>731</fpage>
<lpage>735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000731">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000731">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 lead tetra-acetate. Part IX. The mechanism of reaction with ketone arylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000735</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>M. J.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Gladstone</surname>
<given-names>W. A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>735</fpage>
<lpage>739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000735">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000735">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 epimerisation of 2-hydroxygibbane 1 &lt;b&gt;→&lt;/b&gt; 4a-lactones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000740</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>740</fpage>
<lpage>742</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000740">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000740">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. Synthesis of 1,2,4-triazoles from 1,2-diamino-3-phenylguanidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000742</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
<name><surname>Douraghi-Zadeh</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>742</fpage>
<lpage>746</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000742">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000742">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Ethoxycarbonylhydrazine as a source of 1,2,4-triazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000746</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
<name><surname>Hanks</surname>
<given-names>David R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>746</fpage>
<lpage>751</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000746">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000746">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 fungal metabolites. Part II. The β-oxo-lactone equivalents in rubropunctatin and monascorubrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000751</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hadfield</surname>
<given-names>J. R.</given-names></name>
<name><surname>Holker</surname>
<given-names>J. S. E.</given-names></name>
<name><surname>Stanway</surname>
<given-names>D. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>751</fpage>
<lpage>755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000751">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000751">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 ketones with oxidising agents. Part III. Ring contraction in the boron fluoride-catalysed acetoxylation of 5α-cholestan-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. N.</given-names></name>
<name><surname>Slater</surname>
<given-names>G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>756</fpage>
<lpage>757</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyketo-enols and chelates. Part I. The formation and constitution of xanthophanic enol and the xanthyrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000757</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>Knight</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>757</fpage>
<lpage>762</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000757">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000757">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyketo-enols and chelates. Part II. The chemistry of the xanthophanic enols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000763</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>Knight</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>763</fpage>
<lpage>773</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000763">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000763">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyketo-enols and chelates. Part III. The constitution and chemistry of the glaucophanic enols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000773</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>Knight</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>773</fpage>
<lpage>777</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000773">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000773">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyketo-enols and chelates. Part IV. The by-product in the xanthophanic–glaucophanic enol reaction: 2-acetyl-4,7-alkoxycarbonyl-1,6-dimethylnaphthalane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000777</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>Knight</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>777</fpage>
<lpage>778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000777">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000777">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. The Vilsmeier–Haack reaction with 3- and 4-methoxybenzo[&lt;i&gt;b&lt;/i&gt;]thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
<name><surname>Balucani</surname>
<given-names>D.</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>779</fpage>
<lpage>780</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 senecio alkaloids. Part XIX. The isolation of chlorodeoxysceleratine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000781</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gordon-Gray</surname>
<given-names>C. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>781</fpage>
<lpage>782</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000781">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000781">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzofurano-oxazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000783</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hill</surname>
<given-names>J.</given-names></name>
<name><surname>Ramage</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>783</fpage>
<lpage>784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000783">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000783">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Scriblitifolic acid, a new xanthone from &lt;i&gt;Calophyllum scriblitifolium&lt;/i&gt; Henderson and Wyatt-Smith</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000785</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>785</fpage>
<lpage>796</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000785">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000785">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thiamine. Part II. Origin of the carbon atom in the 2-position of the thiazole component</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000796</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Linnett</surname>
<given-names>P. E.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>796</fpage>
<lpage>799</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000796">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000796">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Submicro-methods for the analysis of organic compounds. Part XXIV. The determination of &lt;i&gt;C&lt;/i&gt;-methyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000799</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Awasthy</surname>
<given-names>A. K.</given-names></name>
<name><surname>Belcher</surname>
<given-names>R.</given-names></name>
<name><surname>Macdonald</surname>
<given-names>A. M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>799</fpage>
<lpage>803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000799">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000799">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 relating to phthiocerol. Part VII. Phthiodiolone A</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000803</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Minnikin</surname>
<given-names>D. E.</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>803</fpage>
<lpage>807</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000803">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000803">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thiocarbonates with lead tetra-acetate and with peracids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000807</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adley</surname>
<given-names>T. J.</given-names></name>
<name><surname>Anisuzzaman</surname>
<given-names>A. K. M.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>807</fpage>
<lpage>812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000807">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000807">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 Kopsia species. Part II. The constitution of fruticosine and fruticosamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000813</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Byrne</surname>
<given-names>J. C.</given-names></name>
<name><surname>Gregory</surname>
<given-names>H.</given-names></name>
<name><surname>Popli</surname>
<given-names>S. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>813</fpage>
<lpage>819</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000813">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000813">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>West African timbers. Part XX. The structure of turraeanthin, an oxygenated tetracyclic triterpene monoacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000820</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
<name><surname>Ekong</surname>
<given-names>D. E. U.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Toft</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>820</fpage>
<lpage>828</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000820">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000820">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 γ-pyrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000828</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mullock</surname>
<given-names>E. B.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>828</fpage>
<lpage>830</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000828">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000828">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclisation of 2-methylbut-3-yn-2-ol. Part I. Cyclisation to aromatic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000830</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chini</surname>
<given-names>P.</given-names></name>
<name><surname>Santambrogio</surname>
<given-names>A.</given-names></name>
<name><surname>Palladino</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>830</fpage>
<lpage>835</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000830">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000830">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclisation of 2-methylbut-3-yn-2-ol. Part II. Cyclisation to cyclo-octatetraene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chini</surname>
<given-names>P.</given-names></name>
<name><surname>Palladino</surname>
<given-names>N.</given-names></name>
<name><surname>Santambrogio</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>836</fpage>
<lpage>840</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitration of 2,3-dimethoxynaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000840</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chang</surname>
<given-names>Clifford W. J.</given-names></name>
<name><surname>Moore</surname>
<given-names>Richard E.</given-names></name>
<name><surname>Scheuer</surname>
<given-names>Paul J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>840</fpage>
<lpage>842</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000840">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000840">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pigments of stick lac. Part II. The structure of laccaic acid A</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000842</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burwood</surname>
<given-names>R.</given-names></name>
<name><surname>Read</surname>
<given-names>G.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Wright</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>842</fpage>
<lpage>851</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000842">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000842">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 in apple peel</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000851</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawrie</surname>
<given-names>W.</given-names></name>
<name><surname>McLean</surname>
<given-names>J.</given-names></name>
<name><surname>Younes</surname>
<given-names>M. El-Garby</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>851</fpage>
<lpage>854</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000851">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000851">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 9,10-anthraquinodimethane and 9-methyleneanthrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Millar</surname>
<given-names>Ian T.</given-names></name>
<name><surname>Richards</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>855</fpage>
<lpage>859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 alkaloids of perennial rye-grass (&lt;i&gt;Lolium perenne&lt;/i&gt; L.). Part III. The synthesis of perlolidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akhtar</surname>
<given-names>M. A.</given-names></name>
<name><surname>Brouwer</surname>
<given-names>W. G.</given-names></name>
<name><surname>Jeffreys</surname>
<given-names>J. A. D.</given-names></name>
<name><surname>Gemenden</surname>
<given-names>C. W.</given-names></name>
<name><surname>Taylor</surname>
<given-names>W. I.</given-names></name>
<name><surname>Seelye</surname>
<given-names>R. N.</given-names></name>
<name><surname>Stanton</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>859</fpage>
<lpage>862</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some West African members of the genus &lt;i&gt;Terminalia&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000863</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ekong</surname>
<given-names>D. E. U.</given-names></name>
<name><surname>Idemudia</surname>
<given-names>O. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>863</fpage>
<lpage>864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000863">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000863">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. The preparation of 4,5,6,7-tetrafluorobenzo[&lt;i&gt;b&lt;/i&gt;]thiophen by a new cyclisation reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000865</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooke</surname>
<given-names>G. M.</given-names></name>
<name><surname>Quasem</surname>
<given-names>Md. Abul</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>865</fpage>
<lpage>869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000865">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000865">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The preparation of 4,5,6,7-tetrafluorobenzo[&lt;i&gt;b&lt;/i&gt;]furan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000869</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooke</surname>
<given-names>G. M.</given-names></name>
<name><surname>Furniss</surname>
<given-names>B. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>869</fpage>
<lpage>873</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000869">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000869">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thermolysis of 3-azabicyclo[3,2,0]hept-6-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000874</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Childs</surname>
<given-names>R. F.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>874</fpage>
<lpage>876</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000874">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000874">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 biochemical transformation of plant steroids. Part I. Biochemical interconversion of the Δ&lt;sup&gt;25(27)&lt;/sup&gt;- and the saturated 25D-or 25L-sapogenins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000876</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
<name><surname>Minato</surname>
<given-names>Hitoshi</given-names></name>
<name><surname>Shimaoka</surname>
<given-names>Ariyoshi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>876</fpage>
<lpage>882</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000876">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000876">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. Dimethyl acetylenedicarboxylate with imidazoles and benzimidazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000882</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Foxton</surname>
<given-names>M. W.</given-names></name>
<name><surname>Abbot</surname>
<given-names>P. J.</given-names></name>
<name><surname>Mills</surname>
<given-names>K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>882</fpage>
<lpage>887</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000882">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000882">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structure and reactivity of anhydro-sugars. Part VII. Syntheses of 5-deoxy-D-&lt;i&gt;xylo&lt;/i&gt;-hexose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000888</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hedgley</surname>
<given-names>E. J.</given-names></name>
<name><surname>Mérész</surname>
<given-names>O.</given-names></name>
<name><surname>Overend</surname>
<given-names>W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>888</fpage>
<lpage>894</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000888">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000888">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 methyl groups on the photolysis of dienones: pentamethylcyclohexa-2,4-dienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>Peter M.</given-names></name>
<name><surname>Hart</surname>
<given-names>Harold</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>895</fpage>
<lpage>903</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Rate enhancement by electron-withdrawal in simple iminopyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000903</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Paddon-Row</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>903</fpage>
<lpage>908</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000903">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000903">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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,7α-Cyclosteroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000909</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>A. R.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>909</fpage>
<lpage>911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000909">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000909">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phenols. Part XI. Oxidation of a model carboxyamide related to 6-methylpretetramid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000912</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Winters</surname>
<given-names>T. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>912</fpage>
<lpage>914</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000912">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000912">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The hydroboronation of (+)-car-3-ene at elevated temperatures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000915</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
<name><surname>Staniland</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>915</fpage>
<lpage>919</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000915">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000915">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclitols. Part XXIV. Selective acetolysis of myoinositol benzyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000919</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Angyal</surname>
<given-names>S. J.</given-names></name>
<name><surname>Randall</surname>
<given-names>M. H.</given-names></name>
<name><surname>Tate</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>919</fpage>
<lpage>922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000919">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000919">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Random depolymerisation of heteropolysaccharides. Part I. Dependence of yield and average molecular weight of homo-oligosaccharides upon monosaccharide distribution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000922</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Painter</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>922</fpage>
<lpage>927</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000922">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000922">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclopropanones and related compounds. Part III. Addition of some isoelectronic molecules to olefins and dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000928</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Halton</surname>
<given-names>B.</given-names></name>
<name><surname>Stevens</surname>
<given-names>I. D. R.</given-names></name>
<name><surname>Watts</surname>
<given-names>C. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>928</fpage>
<lpage>931</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000928">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000928">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 configuration at C-13 in labdanolic and eperuic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000931</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
<name><surname>Renfrew</surname>
<given-names>A. Joyce</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>931</fpage>
<lpage>935</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000931">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000931">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 indanthrone. Part XIII. The constitution of indanthren B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000936</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Malcolm C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>936</fpage>
<lpage>942</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000936">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000936">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 diastereoisomeric 3-methyl-4-phenylpiperidin-4-ols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000942</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casy</surname>
<given-names>A. F.</given-names></name>
<name><surname>Iorio</surname>
<given-names>M. A.</given-names></name>
<name><surname>Pocha</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>942</fpage>
<lpage>944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000942">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000942">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stable alkylidenediphosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000944</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>M. A.</given-names></name>
<name><surname>Tebby</surname>
<given-names>J. C.</given-names></name>
<name><surname>Ronayne</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>944</fpage>
<lpage>947</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000944">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000944">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The compound C&lt;sub&gt;16&lt;/sub&gt;H&lt;sub&gt;18&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;, αβ-dehydrocurvularin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000947</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>947</fpage>
<lpage>948</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000947">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000947">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 naphthazarin and 2-methylnaphthazarin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000949</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cort</surname>
<given-names>L. A.</given-names></name>
<name><surname>Rodriguez</surname>
<given-names>P. A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>949</fpage>
<lpage>952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000949">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000949">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benzoyl isothiocyanate with hydrazine derivatives. Part II. Reaction with some alkyl hydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000952</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Durant</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>952</fpage>
<lpage>956</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000952">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000952">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 crystal and molecular structure of tomatidine hydrobromide and its relation to the steroidal bromosapogenins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000956</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kennard</surname>
<given-names>Olga</given-names></name>
<name><surname>Sanseverino</surname>
<given-names>L. Riva di</given-names></name>
<name><surname>Rollett</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>956</fpage>
<lpage>964</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000956">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000956">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bitter principles of the Cucurbitaceae. Part XV. Cucurbitacins from a hybrid of &lt;i&gt;Lagenaria siceraria&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000964</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Enslin</surname>
<given-names>P. R.</given-names></name>
<name><surname>Holzapfel</surname>
<given-names>C. W.</given-names></name>
<name><surname>Norton</surname>
<given-names>K. Barbara</given-names></name>
<name><surname>Rehm</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>964</fpage>
<lpage>972</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000964">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000964">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bitter principles of the Cucurbitaceae. Part XVI. Stereochemistry of cucurbitacin ring a α-ketols and their acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000972</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Snatzke</surname>
<given-names>G.</given-names></name>
<name><surname>Enslin</surname>
<given-names>P. R.</given-names></name>
<name><surname>Holzapfel</surname>
<given-names>C. W.</given-names></name>
<name><surname>Norton</surname>
<given-names>K. Barbara</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>972</fpage>
<lpage>976</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000972">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000972">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 syntheses of mikanin, combretol, and 3,5,7-trihydroxy-2′-methoxy-flavone, and the purification of flavones by sublimation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000976</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sim</surname>
<given-names>K. Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>976</fpage>
<lpage>979</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000976">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000976">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkyl–oxygen heterolyses in 4-arylpiperidin-4-ols and related esters. Part III. Some 4-alkoxy-4-arylpiperdines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000979</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casy</surname>
<given-names>A. F.</given-names></name>
<name><surname>Pocha</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>979</fpage>
<lpage>983</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000979">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000979">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Indolizines. Part IV. Syntheses from 2-acylmethylene-1-benzyl-1,2-dihydropyridine, phenyl-2-picolyl sulphone, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000983</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Melton</surname>
<given-names>T.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>983</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000983">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000983">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 activity in the 1,1′-binaphthyl series. Energy barriers to racemisation of 8-substituted 1,1′-binaphthyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000988</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooke</surname>
<given-names>Ann S.</given-names></name>
<name><surname>Harris</surname>
<given-names>Margaret M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>988</fpage>
<lpage>992</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000988">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000988">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 carrageenan system of &lt;i&gt;Gigartina skottsbergii&lt;/i&gt; S. et G. Part I. Studies on a fraction of &lt;i&gt;κ&lt;/i&gt;-carrageenan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000992</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cerezo</surname>
<given-names>Alberto S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>992</fpage>
<lpage>997</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000992">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000992">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The synthesis, by twinning, of cyclodepsipeptides related to serratamolide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670000997</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Martin</surname>
<given-names>T. G.</given-names></name>
<name><surname>Schofield</surname>
<given-names>J. A.</given-names></name>
<name><surname>Thomas</surname>
<given-names>Jean O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>997</fpage>
<lpage>1003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670000997">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670000997">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. 4-Nitroindoles and nitrophenylpyrazolones with tertiary amine substituents in the benzene ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001003</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainsworth</surname>
<given-names>D. P.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1003</fpage>
<lpage>1006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001003">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVIII. Aminolysis of 3-aryl-4-bromosydnones, and acid hydrolysis of 3-arylsydnoneimines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001006</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Puranik</surname>
<given-names>G. S.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1006</fpage>
<lpage>1008</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The addition of the Sn–O bond to the carbonyl group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001009</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Symes</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1009</fpage>
<lpage>1016</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001009">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001009">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The free-radical addition of alkanethiols, bromotrichloro-methane, and bromine to hexachloromethylenenorbornene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001017</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alden</surname>
<given-names>C. K.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1017</fpage>
<lpage>1020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001017">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001017">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dithiols. Part XXIII. Optically active forms of 2,3-dimercaptopropanol and related thiols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001021</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anisuzzaman</surname>
<given-names>A. K. M.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1021</fpage>
<lpage>1026</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001021">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001021">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 meliacins and related compounds. Part I. Gedunin and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>M. A.</given-names></name>
<name><surname>Loudon</surname>
<given-names>A. G.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1026</fpage>
<lpage>1034</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXV. The biosynthesis of benzenoid polyacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001035</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fairbrother</surname>
<given-names>J. R. F.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Thaller</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1035</fpage>
<lpage>1038</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001035">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001035">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. Transformations of phenyl-polyacetylenes in the tubers of &lt;i&gt;Dahlia&lt;/i&gt; hybrids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001038</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Safe</surname>
<given-names>S.</given-names></name>
<name><surname>Thaller</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1038</fpage>
<lpage>1041</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001038">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001038">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic substitution of conjugated eighteen-membered ring systems. Novel conformational effects in mono-substituted [18]annulenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calder</surname>
<given-names>I. C.</given-names></name>
<name><surname>Garratt</surname>
<given-names>P. J.</given-names></name>
<name><surname>Longuet-Higgins</surname>
<given-names>H. C.</given-names></name>
<name><surname>Sondheimer</surname>
<given-names>F.</given-names></name>
<name><surname>Wolovsky</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1041</fpage>
<lpage>1044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 amines. Part IV. 3,17-Diaminoandrostane derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>M.</given-names></name>
<name><surname>Parnell</surname>
<given-names>E. W.</given-names></name>
<name><surname>Rosenbaum</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1045</fpage>
<lpage>1052</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 identification of some &lt;i&gt;N&lt;/i&gt;-methylated aminonitrophenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Amery</surname>
<given-names>G. W.</given-names></name>
<name><surname>Corbett</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1053</fpage>
<lpage>1057</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cycloheptatriene and tropylium metal complexes. Part IV. Preparation of 7-&lt;i&gt;exo&lt;/i&gt;-substituted tricarbonylcycloheptatrienechromiums</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001057</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Smith</surname>
<given-names>G. H.</given-names></name>
<name><surname>Valentine</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1057</fpage>
<lpage>1061</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001057">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001057">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cycloheptatriene and tropylium metal complexes. Part V. 7-&lt;i&gt;endo&lt;/i&gt;-Substituted tricarbonylcycloheptatrienechromiums</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001061</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Smith</surname>
<given-names>G. H.</given-names></name>
<name><surname>Valentine</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1061</fpage>
<lpage>1065</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001061">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001061">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polysaccharides of soy-beans. Part III. Extraction and fractionation of polysaccharides from cotyledon meal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001065</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Begbie</surname>
<given-names>R.</given-names></name>
<name><surname>Hamilton</surname>
<given-names>A.</given-names></name>
<name><surname>Whyte</surname>
<given-names>J. N. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1065</fpage>
<lpage>1070</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001065">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001065">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polysaccharides of soy-beans. Part IV. Partial hydrolysis of the acidic polysaccharide complex from cotyledon meal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001071</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Cottrell</surname>
<given-names>I. W.</given-names></name>
<name><surname>Egan</surname>
<given-names>(Mrs.) Sylvia V.</given-names></name>
<name><surname>Morrison</surname>
<given-names>I. M.</given-names></name>
<name><surname>Whyte</surname>
<given-names>J. N. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1071</fpage>
<lpage>1080</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001071">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001071">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polysaccharides of soy-beans. Part V. Acidic polysaccharides from the hulls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001080</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Hunt</surname>
<given-names>K.</given-names></name>
<name><surname>Morrison</surname>
<given-names>I. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1080</fpage>
<lpage>1086</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001080">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001080">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gum tragacanth. Part III. The characterisation of three aldobiouronic acids as minor partial hydrolysis products from tragacanthic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001086</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. B.</given-names></name>
<name><surname>Fraser</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1086</fpage>
<lpage>1088</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001086">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001086">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. Active esters of some 5-aminoimidazole-4-carboxylic acids and their use in the preparation of 5-aminoimidazole-4-carboxyamides and their nucleoside and nucleotide derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001088</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burrows</surname>
<given-names>I. E.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1088</fpage>
<lpage>1093</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Indenylidenetriphenylphosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001093</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crofts</surname>
<given-names>P. C.</given-names></name>
<name><surname>Williamson</surname>
<given-names>M. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1093</fpage>
<lpage>1095</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001093">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001093">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. 1,3-di-&lt;i&gt;O&lt;/i&gt;-cyanophenyltriazene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stevens</surname>
<given-names>M. F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1096</fpage>
<lpage>1098</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2,2,2-Triphenyl-1,2-oxaphosph(V)olan and -oxa-ars(V)olan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hands</surname>
<given-names>A. R.</given-names></name>
<name><surname>Mercer</surname>
<given-names>A. J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1099</fpage>
<lpage>1100</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part XVII. A new method of effecting Pschorr-type cyclisations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001101</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Robson</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1101</fpage>
<lpage>1102</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001101">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001101">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part XLIV. Steroid acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001102</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jennings</surname>
<given-names>J. P.</given-names></name>
<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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1102</fpage>
<lpage>1108</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001102">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001102">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 Eleagnine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001109</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Kenneally</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1109</fpage>
<lpage>1110</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001109">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001109">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclobutanetetracarboxylic dianhydride from the reaction of tetramethyl tricyclo[4,2,2,0&lt;sup&gt;2,5&lt;/sup&gt;]dec-9-ene-3,4,7,8-tetracarboxylate with nitric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001111</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Starr</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1111</fpage>
<lpage>1111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001111">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001111">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinolizines. Part X. Experiments in the synthesis of 2-alkylquinolizinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001112</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>T. L.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1112</fpage>
<lpage>1114</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 two 3,3,3-triarylpropenes and two 2-methyl-3,3,3-triarylpropenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1115</fpage>
<lpage>1120</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 di-imide reduction of aromatic aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001120</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Curry</surname>
<given-names>D. C.</given-names></name>
<name><surname>Uff</surname>
<given-names>B. C.</given-names></name>
<name><surname>Ward</surname>
<given-names>N. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1120</fpage>
<lpage>1121</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001120">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001120">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thio-sugars. Part III. The thioseptanose ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001121</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>J. M.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1121</fpage>
<lpage>1130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001121">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001121">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hemithioacetals: analogues of thiosugars with sulphur in the ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001130</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>J. M.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1130</fpage>
<lpage>1134</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001130">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001130">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 acetic anhydride on 1-nitroso-4-phenyl-4-piperidinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001134</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheesman</surname>
<given-names>D. G.</given-names></name>
<name><surname>Garside</surname>
<given-names>P.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>A. C.</given-names></name>
<name><surname>Waring</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1134</fpage>
<lpage>1136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001134">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001134">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nitrous acid on &lt;i&gt;NNN&lt;/i&gt;′&lt;i&gt;N&lt;/i&gt;′-tetramethyl-&lt;i&gt;p&lt;/i&gt;-phenylenediamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>J. F.</given-names></name>
<name><surname>Fooks</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1136</fpage>
<lpage>1138</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Methanesulphonyl and benzenesulphonyl derivatives of indazolin-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001139</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Way</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1139</fpage>
<lpage>1141</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001139">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001139">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photochemistry. Part IV. Photonucleophilic substitution reactions of monosubstituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Bunce</surname>
<given-names>N. J.</given-names></name>
<name><surname>Thomson</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1142</fpage>
<lpage>1145</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Monomeric lignin sulphonic acids. Part II.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001145</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parrish</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1145</fpage>
<lpage>1150</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001145">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001145">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 chlorofluoroalkanes with triethyl phosphite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001150</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Platt</surname>
<given-names>A. E.</given-names></name>
<name><surname>Tittle</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1150</fpage>
<lpage>1152</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001150">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001150">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 arylbenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001153</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Liang</surname>
<given-names>Katherine S. Y.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
<name><surname>Williams</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1153</fpage>
<lpage>1153</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001153">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001153">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dihalogenoketens with carbodi-imides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001154</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hull</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1154</fpage>
<lpage>1155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001154">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001154">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and Walden inversion. Part LX. Some reactions of the epimeric 5α-cholestan-1-ols and the solvolysis of their toluene-p-sulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001155</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Lack</surname>
<given-names>Ruth E.</given-names></name>
<name><surname>Sharma</surname>
<given-names>S. C.</given-names></name>
<name><surname>Smith</surname>
<given-names>Lorraine R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1155</fpage>
<lpage>1159</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001155">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001155">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The stereochemistry of the reduction of cyclohexanones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001159</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Regan</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1159</fpage>
<lpage>1163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001159">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001159">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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, sulphonation, and nitration of pyrrolo[1,2-&lt;i&gt;a&lt;/i&gt;]quinoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Tuck</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1164</fpage>
<lpage>1167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;meso&lt;/i&gt;-reactivity of porphyrins and related compounds. Part III. Deuteriation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001168</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonnett</surname>
<given-names>R.</given-names></name>
<name><surname>Gale</surname>
<given-names>I. A. D.</given-names></name>
<name><surname>Stephenson</surname>
<given-names>G. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1168</fpage>
<lpage>1172</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001168">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001168">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrimidines. Part II. Nucleophilic substitution reactions of ethyl 4-chloro-2-methylthiopyrimidine-5-carboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001172</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shadbolt</surname>
<given-names>R. S.</given-names></name>
<name><surname>Ulbricht</surname>
<given-names>T. L. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1172</fpage>
<lpage>1178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001172">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001172">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-oxy-derivatives. Part VII. Some 5,6-dihydro-5-oxo-3-phenyl-1,4-dioxazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001178</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McHale</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1178</fpage>
<lpage>1179</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001178">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001178">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hemicellulose of sisal fibre (&lt;i&gt;Agave sisalana&lt;/i&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001179</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gupta</surname>
<given-names>P. C. Das</given-names></name>
<name><surname>Mukherjee</surname>
<given-names>P. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1179</fpage>
<lpage>1182</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001179">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001179">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Displacement reactions of acyclic carbohydrate derivatives. Part II. A 1,4-methoxyl group migration following acetal participation: 4-&lt;i&gt;O&lt;/i&gt;-methyl-L-lyxose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hughes</surname>
<given-names>N. A.</given-names></name>
<name><surname>Speakman</surname>
<given-names>P. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1182</fpage>
<lpage>1185</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Displacement reactions of acyclic carbohydrate derivatives. Part III. Aldehyde group participation in 2,3,5-tri-&lt;i&gt;O&lt;/i&gt;-benzyl-4-&lt;i&gt;O&lt;/i&gt;-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl-aldehydo-D-ribose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001186</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hughes</surname>
<given-names>N. A.</given-names></name>
<name><surname>Speakman</surname>
<given-names>P. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1186</fpage>
<lpage>1187</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001186">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001186">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 decomposition of 4-azido-4-&lt;i&gt;p&lt;/i&gt;-nitrophenylbutan-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001188</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Donald</surname>
<given-names>A. S. R.</given-names></name>
<name><surname>Marks</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1188</fpage>
<lpage>1189</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001188">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001188">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The preparation of 4,5,6,7-tetrafluoroindole by a new cyclisation reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001189</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooke</surname>
<given-names>G. M.</given-names></name>
<name><surname>Rutherford</surname>
<given-names>R. J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1189</fpage>
<lpage>1191</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001189">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001189">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;OO&lt;/i&gt;-dialkylphosphorodithioate derivatives of 1,3,5-triazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001192</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Osborne</surname>
<given-names>G. O.</given-names></name>
<name><surname>Page</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1192</fpage>
<lpage>1194</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001192">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001192">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrogen-containing carbohydrate derivatives. Part XIV. Configurational studies on amino-sugars using cuprammonium solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001194</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlow</surname>
<given-names>C. B.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1194</fpage>
<lpage>1197</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001194">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001194">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 closer examination of the mechanism for photolytic ring-opening of cyclohexa-2,4-dienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001197</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>Peter M.</given-names></name>
<name><surname>Hart</surname>
<given-names>Harold</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1197</fpage>
<lpage>1202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001197">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001197">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrimidines. Part XV. The nitrosation of 4,6-dimethyl- and 4-methyl-6-phenyl-pyrimidin-2-ols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hurst</surname>
<given-names>D. T.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>Tute</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1202</fpage>
<lpage>1204</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrimidines. Part XVI. Syntheses of bipyrimidinyls and of halogeno- and amidino-pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001204</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caton</surname>
<given-names>M. P. L.</given-names></name>
<name><surname>Hurst</surname>
<given-names>D. T.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>Hunt</surname>
<given-names>R. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1204</fpage>
<lpage>1209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001204">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001204">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proof of the imidoyl phosphate intermediate for oxidative phosphorylation in [&lt;sup&gt;18&lt;/sup&gt;O]dimethylformamide solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001210</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>Jack S.</given-names></name>
<name><surname>Lapidot</surname>
<given-names>Aviva</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1210</fpage>
<lpage>1213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001210">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001210">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Neighbouring-group participation by sulphinyl-oxygen. Part II. A Walden cycle at a sulphur atom</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cinquini</surname>
<given-names>M.</given-names></name>
<name><surname>Colonna</surname>
<given-names>S.</given-names></name>
<name><surname>Montanari</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1213</fpage>
<lpage>1217</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Three diastereoisomeric 4,6-linked bileucofisetinidins from the heartwood of &lt;i&gt;Acacia mearnsii&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001217</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drewes</surname>
<given-names>S. E.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
<name><surname>Eggers</surname>
<given-names>S. H.</given-names></name>
<name><surname>Feeney</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1217</fpage>
<lpage>1227</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001217">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001217">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 7β-acetoxy-5α-cholestan-4-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>A. R.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1227</fpage>
<lpage>1232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrrolizidine alkaloids. Biosynthesis of the angelate component of heliosupine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001233</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crout</surname>
<given-names>D. H. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1233</fpage>
<lpage>1234</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001233">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001233">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nitroquinols and their methyl ethers and benzenesulphonyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001235</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1235</fpage>
<lpage>1238</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 Steroid group. Part LXXVII. Derivatives of 22,23-di-hydroneoergosterol (3β-hydroxy-19-norergosta-5,7,9-triene)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001238</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McGinnis</surname>
<given-names>E. L.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Morris</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1238</fpage>
<lpage>1241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001238">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001238">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Perfluoroalkyl derivatives of nitrogen. Part XXV. The reactions of tristrifluoromethylhydroxylamine and mercuric bistrifluoromethylamide with unsaturated systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001241</article-id><contrib-group><contrib contrib-type="author">
<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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1241</fpage>
<lpage>1249</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIX. Preparation and nucleophilic reactions of polyhalogeno-substituted &lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001249</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellas</surname>
<given-names>M.</given-names></name>
<name><surname>Price</surname>
<given-names>D.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1249</fpage>
<lpage>1254</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 properties of 8-pyridylpurines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001254</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>F.</given-names></name>
<name><surname>Rashi</surname>
<given-names>M.</given-names></name>
<name><surname>Kleiner</surname>
<given-names>M.</given-names></name>
<name><surname>Knafo</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1254</fpage>
<lpage>1260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001254">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001254">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinones. Part VIII. Dehydro-α- and -β-lapachone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burnett</surname>
<given-names>A. R.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1261</fpage>
<lpage>1264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2-alkoxy-2-phenylacetamido-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lucente</surname>
<given-names>G.</given-names></name>
<name><surname>Pantanella</surname>
<given-names>F.</given-names></name>
<name><surname>Romeo</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1264</fpage>
<lpage>1264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 intermediates. Part I. The influence of electronic and steric effects on the direction of hydrocarboxylation of acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bird</surname>
<given-names>C. W.</given-names></name>
<name><surname>Hollins)</surname>
<given-names>E. M. Briggs (née</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1265</fpage>
<lpage>1267</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Investigations on plants of West Africa. Part VI. Constituents of &lt;i&gt;Bersama abyssinica&lt;/i&gt; Fres. subsp. Paullinioides Verdc. (Melianthaceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001268</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor-Smith</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1268</fpage>
<lpage>1269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 reduction of thiazolium salts with sodium borohydride. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clarke</surname>
<given-names>G. M.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1269</fpage>
<lpage>1273</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 optical rotatory dispersion of tetrahydropyranyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001273</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Mose</surname>
<given-names>W. P.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
<name><surname>Holder</surname>
<given-names>G. M.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1273</fpage>
<lpage>1276</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001273">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001273">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 biphenylenes. Part III. Syntheses of benzo- and dibenzo-biphenylenes &lt;i&gt;via&lt;/i&gt; aryne intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001276</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>J. W.</given-names></name>
<name><surname>Jones</surname>
<given-names>(Miss) S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1276</fpage>
<lpage>1278</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001276">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001276">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. The [1,2,3]-triazolo[5,1-&lt;i&gt;c&lt;/i&gt;][1,2,4]benzotriazine ring system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001279</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tennant</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1279</fpage>
<lpage>1283</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001279">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001279">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 reductive amination. Part I. Aminoalkylpiperidines from 2-hydroxy-1,6-hexanedial</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001284</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>David H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1284</fpage>
<lpage>1289</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001284">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001284">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 (±)-pulvilloric acid and of (±) methyl dihydropul-villorate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001289</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bullimore</surname>
<given-names>B. K.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
<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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1289</fpage>
<lpage>1293</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001289">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001289">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 note on the formation of 4,4′-dihydroxy-3,3′,5,5′-tetraiodobenzo-phenone from 4-hydroxy-3,5-di-iodophenylpyruvic acid and 4-hydroxy-3,5-di-iodobenzoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001294</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Matsuura</surname>
<given-names>Teruo</given-names></name>
<name><surname>Nakashima</surname>
<given-names>Ruka</given-names></name>
<name><surname>Ohe</surname>
<given-names>Takehiro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1294</fpage>
<lpage>1295</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001294">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001294">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and biosynthesis. Part XIV. (Alkaloids from Croton species. Part VII.) The biosynthesis of crotonosine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001295</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Bhakuni</surname>
<given-names>D. S.</given-names></name>
<name><surname>Chapman</surname>
<given-names>G. M.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
<name><surname>Stuart</surname>
<given-names>K. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1295</fpage>
<lpage>1298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001295">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001295">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Iodonium salt synthesis. Evidence for the formation of isomers in the synthesis of diaryliodonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001298</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Count</surname>
<given-names>D. J. Le</given-names></name>
<name><surname>Reid</surname>
<given-names>J. A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1298</fpage>
<lpage>1301</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereochemically identical biflavanols from the bark tannins of &lt;i&gt;Acacia mearnsii&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drewes</surname>
<given-names>S. E.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
<name><surname>Saayman</surname>
<given-names>H. M.</given-names></name>
<name><surname>Eggers</surname>
<given-names>S. H.</given-names></name>
<name><surname>Feeney</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1302</fpage>
<lpage>1308</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. Further addition reactions of tributyltin methoxide and of bistributyltin oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001309</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bloodworth</surname>
<given-names>A. J.</given-names></name>
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Vasishtha</surname>
<given-names>S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1309</fpage>
<lpage>1313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001309">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001309">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Addition reactions of dibutyltin dimethoxide and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001313</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1313</fpage>
<lpage>1317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 (±)-eschscholtzine. The absolute configuration of (–)-argemonine, (–)-eschscholtzine, and related alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>A. C.</given-names></name>
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1317</fpage>
<lpage>1323</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinone epoxides. Part II. Synthesis of (±)-terreic acid and some related epoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rashid</surname>
<given-names>A.</given-names></name>
<name><surname>Read</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1323</fpage>
<lpage>1325</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 method for the preparation of amides and esters of di-n-alkylphosphinic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001326</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Silver</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1326</fpage>
<lpage>1326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001326">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001326">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tembamide from &lt;i&gt;Fagara hyemalis&lt;/i&gt;(St. Hill.) Engler</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albónico</surname>
<given-names>S. M.</given-names></name>
<name><surname>Kuck</surname>
<given-names>A. M.</given-names></name>
<name><surname>Deulofeu</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1327</fpage>
<lpage>1328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anthraquinone dyes. Part III. Nitration of toluoylbenzoic acid and cyclisation of the corresponding amino-acids to amino-derivatives of 2-methylanthraquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arient</surname>
<given-names>J.</given-names></name>
<name><surname>Šlosar</surname>
<given-names>J.</given-names></name>
<name><surname>Štěrba</surname>
<given-names>V.</given-names></name>
<name><surname>Obruba</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1329</fpage>
<lpage>1331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anthraquinone dyes. Part IV. Nitration of 2-(3-chloro-4-methyl-benzoyl)benzoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arient</surname>
<given-names>J.</given-names></name>
<name><surname>Šlosar</surname>
<given-names>J.</given-names></name>
<name><surname>Štěrba</surname>
<given-names>V.</given-names></name>
<name><surname>Obruba</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1331</fpage>
<lpage>1334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dipeptides containing DL-&lt;i&gt;p&lt;/i&gt;-trimethylsilyphenylalanine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Frankel</surname>
<given-names>Max</given-names></name>
<name><surname>Gertner</surname>
<given-names>David</given-names></name>
<name><surname>Shenhar</surname>
<given-names>Avinoam</given-names></name>
<name><surname>Zilkha</surname>
<given-names>Albert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1334</fpage>
<lpage>1336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Transacylation reactions of amides with acids and anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001337</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Michman</surname>
<given-names>Michael</given-names></name>
<name><surname>Patai</surname>
<given-names>Saul</given-names></name>
<name><surname>Shenfeld</surname>
<given-names>Izhak</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1337</fpage>
<lpage>1340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Clemmensen reduction. Part IV. 1,4-Diketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001340</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buchanan</surname>
<given-names>J. G. St. C.</given-names></name>
<name><surname>Davis</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1340</fpage>
<lpage>1343</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001340">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001340">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photochemistry. Part III. The photocyclisation of 4-styrylpyrimidine to benzo[&lt;i&gt;f&lt;/i&gt;]quinazoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001343</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Loader</surname>
<given-names>C. E.</given-names></name>
<name><surname>Timmons</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1343</fpage>
<lpage>1344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001343">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001343">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cleavage of 6-methoxy-2-(2,4,6-trimethoxybenzoyl)coumaran-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001345</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryant</surname>
<given-names>Rhys</given-names></name>
<name><surname>Haslam</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1345</fpage>
<lpage>1345</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001345">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001345">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;i&gt;O&lt;/i&gt;-α-D-galactopyranosylglycerol from &lt;i&gt;Laurencia pinnatifida&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Durham</surname>
<given-names>L. J.</given-names></name>
<name><surname>Kanazawa</surname>
<given-names>Y.</given-names></name>
<name><surname>Safe</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1346</fpage>
<lpage>1347</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The complete structure of melianone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lavie</surname>
<given-names>D.</given-names></name>
<name><surname>Jain</surname>
<given-names>Mahendra K.</given-names></name>
<name><surname>Kirson</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1347</fpage>
<lpage>1351</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001347">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part II. The electrolysis of dialkyl sodiomalonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001352</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
<name><surname>Parkin</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1352</fpage>
<lpage>1355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001352">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001352">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 organophosphorus compounds. Part XX. A route to pyrophosphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001356</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. E.</given-names></name>
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1356</fpage>
<lpage>1360</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001356">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001356">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 abbeokutone, a diterpene from &lt;i&gt;Didymosalpinx abbeokutae&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001360</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1360</fpage>
<lpage>1362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001360">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001360">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 derivatives of maleic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001362</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mufti</surname>
<given-names>A. S.</given-names></name>
<name><surname>Poller</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1362</fpage>
<lpage>1364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001362">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001362">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 protection of terminal ethynyl groups in Grignard syntheses</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Thompson</surname>
<given-names>A. R.</given-names></name>
<name><surname>Walton</surname>
<given-names>D. R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1364</fpage>
<lpage>1366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001364">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part XLVI. Steroid 17-carboxylic acids (etianic acids) and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001366</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gottarelli</surname>
<given-names>G.</given-names></name>
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1366</fpage>
<lpage>1370</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001366">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001366">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part XLVII. Cholanic acids, related steroid acids and their esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001370</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gottarelli</surname>
<given-names>G.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1370</fpage>
<lpage>1373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001370">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001370">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-alkanethiols from amino-alcohols &lt;i&gt;via&lt;/i&gt; aminoalkyl sulphates and thiazolidinethiones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Owen</surname>
<given-names>Terence C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1373</fpage>
<lpage>1376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 oxygen heterocycles. Part IV. The mass spectra of some complex lignans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001376</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pelter</surname>
<given-names>Andrew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1376</fpage>
<lpage>1380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001376">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001376">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bi-indenyls. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
<name><surname>Spanswick</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1380</fpage>
<lpage>1381</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rearrangements of oxo-dicyclopentadienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001382</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Hudec</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>R. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1382</fpage>
<lpage>1385</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001382">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Interconversion of 5-arylbicyclo[2,2,1]hept-2-en-7-ones and 6-arylbicyclo[3,2,0]hept-3-en-2-ones by acid and by light</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Besford</surname>
<given-names>L. S.</given-names></name>
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Cooper</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1385</fpage>
<lpage>1391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 polyaryl-bicyclo[2,2,1]hept-2-en-7-ones and bicyclo-[3,2,0]hept-3-en-2-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001391</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Warrell</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1391</fpage>
<lpage>1400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001391">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001391">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The dimethanesulphonates of 3-phenylthiopropane-1,2-diol and of 2-phenylthiopropane-1,3-diol; their reactions with nucleophiles, and rearrangements through sulphonium ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001400</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baig</surname>
<given-names>M. V. A.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1400</fpage>
<lpage>1407</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001400">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001400">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of mopanin from &lt;i&gt;Colophospermum mopane&lt;/i&gt; and interrelation of flavonoid components of &lt;i&gt;Peltogyne&lt;/i&gt; spp.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001407</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drewes</surname>
<given-names>S. E.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1407</fpage>
<lpage>1410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001407">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001407">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 reduction of thiazolium salts with sodium borohydride. Part II. The mechanism and stereochemistry of reduction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clarke</surname>
<given-names>G. M.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1411</fpage>
<lpage>1414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LVIII. Double Skraup reaction to diaza-derivatives of some carcinogenic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001415</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dufour</surname>
<given-names>M.</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1415</fpage>
<lpage>1416</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001415">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001415">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 conformational free energies of allylic hydroxy-, acetoxy-, and methoxy-groups in cyclohexenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001417</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferrier</surname>
<given-names>R. J.</given-names></name>
<name><surname>Prasad</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1417</fpage>
<lpage>1420</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001417">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001417">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phosphorylation. Part XXX. Phosphorylation &lt;i&gt;via&lt;/i&gt; carbonium, phosphonium, and sulphonium intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kaye</surname>
<given-names>Howard</given-names></name>
<name><surname>Todd</surname>
<given-names>Lord</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1420</fpage>
<lpage>1423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the chemistry of melanins. Part III. Synthesis of 5,6-dihydroxyindoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001424</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mishra</surname>
<given-names>S. N.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1424</fpage>
<lpage>1427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001424">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001424">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the chemistry of melanins. Part IV. Oxidation of 5,6-dimethoxyindoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mishra</surname>
<given-names>S. N.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1428</fpage>
<lpage>1431</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the chemistry of melanins. Part V. Investigations on the specific deuteriation of 5,6-dihydroxyindoline and 5,6-dihydroxyindole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mishra</surname>
<given-names>S. N.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1431</fpage>
<lpage>1435</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. Synthesis of 1,2-disubstituted ferrocenes by metallation and nucleophilic substitution reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001436</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hadlington</surname>
<given-names>M.</given-names></name>
<name><surname>Rockett</surname>
<given-names>B. W.</given-names></name>
<name><surname>Nelhans</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1436</fpage>
<lpage>1440</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001436">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001436">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 (±)-glaucine methopicrate by phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001440</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>Tetsuji</given-names></name>
<name><surname>Noguchi</surname>
<given-names>Isao</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1440</fpage>
<lpage>1443</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001440">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001440">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 isomeric dithenyl sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>E.</given-names></name>
<name><surname>Moodie</surname>
<given-names>I. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1443</fpage>
<lpage>1444</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Purine studies. Part V. Formation and aminolysis of some methylthiopurines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001445</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Ford</surname>
<given-names>P. W.</given-names></name>
<name><surname>Tratt</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1445</fpage>
<lpage>1449</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001445">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001445">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 trifluoromethylcarbene with &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-but-2-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001450</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1450</fpage>
<lpage>1454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001450">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001450">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;N&lt;/i&gt;-methyl derivatives of 1,3-diamino-2-phenylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bedford</surname>
<given-names>G. R.</given-names></name>
<name><surname>Landquist</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1454</fpage>
<lpage>1456</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bi-indenyls. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001456</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
<name><surname>Spanswick</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1456</fpage>
<lpage>1457</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001456">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001456">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photochemistry. Part IV. The formation of 1- and 3-cyclohexylbenz[&lt;i&gt;h&lt;/i&gt;]isoquinoline in the course of the photocyclodehydrogenation of 4-stilbazole to benz[&lt;i&gt;h&lt;/i&gt;]isoquinoline in cyclohexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001457</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Loader</surname>
<given-names>C. E.</given-names></name>
<name><surname>Timmons</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1457</fpage>
<lpage>1460</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001457">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001457">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 epoxides. Part I. α-Substituted epoxy-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001460</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greenfield</surname>
<given-names>S.</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>Kashman</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1460</fpage>
<lpage>1469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001460">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001460">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 route to α-chloroalkylsilanes. Use of chloroalkyl-lithium compounds and chloroalkylmagnesium halides as &lt;i&gt;in situ&lt;/i&gt; reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001470</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bamford</surname>
<given-names>W. R.</given-names></name>
<name><surname>Pant</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1470</fpage>
<lpage>1472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001470">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001470">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some chromens and naphthopyrans with bromine and chlorine. Part V. Preparation of 6,6-disubstituted 4,5-dihydronaphtho(2′,1′:2,3)pyran-5-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001472</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abbott</surname>
<given-names>J. B.</given-names></name>
<name><surname>France</surname>
<given-names>C. J.</given-names></name>
<name><surname>Livingstone</surname>
<given-names>R.</given-names></name>
<name><surname>Morrey</surname>
<given-names>D. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1472</fpage>
<lpage>1475</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001472">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001472">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 uronic acid materials. Part XXI. Some structural features of &lt;i&gt;Acacia arabica&lt;/i&gt; gum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001476</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. M. W.</given-names></name>
<name><surname>Hirst</surname>
<given-names>Sir Edmund</given-names></name>
<name><surname>Stoddart</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1476</fpage>
<lpage>1486</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001476">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001476">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Reactions of some &lt;i&gt;p&lt;/i&gt;-quinones with aliphatic and aromatic aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001486</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>Ellis</surname>
<given-names>J. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1486</fpage>
<lpage>1490</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001486">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001486">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryl-substituted derivatives of 4,4′-bipyridylium salts: their spectroscopic properties and stereochemistry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001491</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Downes</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1491</fpage>
<lpage>1493</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001491">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001491">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 properties of some pyrazolyl ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001494</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
<name><surname>Foster</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1494</fpage>
<lpage>1497</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001494">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001494">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 acetylation of anthracene in nitrobenzene solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001498</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1498</fpage>
<lpage>1498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001498">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001498">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 5,6-chrysenequinodimethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>D.</given-names></name>
<name><surname>Millar</surname>
<given-names>Ian T.</given-names></name>
<name><surname>Richards</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1499</fpage>
<lpage>1503</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 javose (6-deoxy-2-&lt;i&gt;O&lt;/i&gt;-methyl-D-allose)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001503</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Husain</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1503</fpage>
<lpage>1506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001503">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001503">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 methods in peptide synthesis. Part IV. N &lt;b&gt;→&lt;/b&gt; S transfer of &lt;i&gt;N&lt;/i&gt;-&lt;i&gt;o&lt;/i&gt;-nitrophenylsulphenyl groups in cysteine peptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Phocas</surname>
<given-names>I.</given-names></name>
<name><surname>Yovanidis</surname>
<given-names>C.</given-names></name>
<name><surname>Photaki</surname>
<given-names>I.</given-names></name>
<name><surname>Zervas</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1506</fpage>
<lpage>1509</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 Leuckart reaction with 4-t-butylcyclohexanone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. G.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Whateley</surname>
<given-names>T. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1509</fpage>
<lpage>1512</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXI. Thermal decomposition of diazonium sulphates from alkoxy-&lt;i&gt;N&lt;/i&gt;-alkyl-2-aminobenzanilides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001513</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Leonard</surname>
<given-names>J. A.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
<name><surname>Todd</surname>
<given-names>Alan R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1513</fpage>
<lpage>1518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001513">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001513">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXII. Catalysed decomposition of diazonium fluoroborates from alkoxy-&lt;i&gt;N&lt;/i&gt;-alkyl-2-aminobenzanilides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001518</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
<name><surname>Todd</surname>
<given-names>Alan R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1518</fpage>
<lpage>1525</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001518">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001518">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photocyclisation of some stilbene analogues. Synthesis of dibenzo[&lt;i&gt;a&lt;/i&gt;,&lt;i&gt;l&lt;/i&gt;]pyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001525</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1525</fpage>
<lpage>1527</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001525">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001525">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrazinolysis of some purines and pyrimidines and their related nucleosides and nucleotides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001528</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hayes</surname>
<given-names>D. H.</given-names></name>
<name><surname>Hayes-Baron</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1528</fpage>
<lpage>1533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001528">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001528">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 replacement of the hydrazino-group by hydrogen and deuterium in azanaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001533</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Catterall</surname>
<given-names>Gordon</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1533</fpage>
<lpage>1541</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001533">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001533">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVII. 2-Pyridones with dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001542</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Tasker</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1542</fpage>
<lpage>1543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001542">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001542">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Ethyl pteridine-4-carboxylate and some methyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001543</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1543</fpage>
<lpage>1547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001543">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001543">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 tetraphenyldiphosphine with aromatic carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001547</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Sheldon</surname>
<given-names>R. A.</given-names></name>
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1547</fpage>
<lpage>1552</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001547">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001547">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Overcrowded molecules. Part II. The interaction of diphenylketen with 2-benzylidene-1,3-indanedione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001552</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heller</surname>
<given-names>H. G.</given-names></name>
<name><surname>Auld</surname>
<given-names>D.</given-names></name>
<name><surname>Salisbury</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1552</fpage>
<lpage>1554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001552">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001552">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dimeric by-products of the preparation of 2,4-dimethoxybenzyl cyanide from 2,4-dimethoxy-β-nitrostyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burns</surname>
<given-names>W. D. P.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Staniland</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1554</fpage>
<lpage>1556</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 long-chain acids. Part VIII. 9,10,18-Trihydroxyoctadecanoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001556</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Goodburn</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1556</fpage>
<lpage>1558</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001556">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001556">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the 1,2,5,6-tetrahydropyridine series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001558</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taub</surname>
<given-names>D.</given-names></name>
<name><surname>Kuo</surname>
<given-names>C. H.</given-names></name>
<name><surname>Wendler</surname>
<given-names>N. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1558</fpage>
<lpage>1564</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001558">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001558">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,8-Naphthyridines. Part II. Preparation and some reactions of 2-substituted derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001564</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hawes</surname>
<given-names>E. M.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1564</fpage>
<lpage>1568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001564">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001564">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The addition of dimethylketen to quinoline, isoquinoline, and phenanthridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001569</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pratt</surname>
<given-names>R. N.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. A.</given-names></name>
<name><surname>Proctor</surname>
<given-names>S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1569</fpage>
<lpage>1575</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001569">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001569">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sesquiterpenoids. Part XVI. A new synthetic method for α-methylene-γ-lactones; total synthesis of (±)-isoalantolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001575</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Minato</surname>
<given-names>Hitoshi</given-names></name>
<name><surname>Horibe</surname>
<given-names>Isao</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1575</fpage>
<lpage>1577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001575">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001575">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 xylan from perennial rye-grass (&lt;i&gt;Lolium perenne&lt;/i&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alam</surname>
<given-names>M.</given-names></name>
<name><surname>McIlroy</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1577</fpage>
<lpage>1580</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 routes to benz- and naphth-indenoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001581</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Antaki</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1581</fpage>
<lpage>1582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001581">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001581">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 linderone and methyl-inderone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001583</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lee</surname>
<given-names>H. H.</given-names></name>
<name><surname>Tan</surname>
<given-names>C. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1583</fpage>
<lpage>1585</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001583">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001583">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the chlorination of naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, and several chloro-methylnaphthalenes with sulphuryl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001586</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Suzuki</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1586</fpage>
<lpage>1590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001586">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001586">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1-methylnaphthalene by molecular chlorine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cum</surname>
<given-names>G.</given-names></name>
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1590</fpage>
<lpage>1598</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some indenoisoxazole derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001598</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bianchi</surname>
<given-names>G.</given-names></name>
<name><surname>Gandolfi</surname>
<given-names>R.</given-names></name>
<name><surname>Grünanger</surname>
<given-names>P.</given-names></name>
<name><surname>Perotti</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1598</fpage>
<lpage>1602</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001598">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001598">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 lichen constituents. Part III. Haemathamnolic acid: a new β-orcinol depside from &lt;i&gt;Pertusaria rhodesiaca&lt;/i&gt; vainio</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harper</surname>
<given-names>S. H.</given-names></name>
<name><surname>Letcher</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1603</fpage>
<lpage>1608</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Diels–Alder reactions of perfluorocyclopentadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001608</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Harrison</surname>
<given-names>A. C.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Orrell</surname>
<given-names>K. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1608</fpage>
<lpage>1621</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001608">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001608">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Rearrangements at C-21 in the hopane series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001622</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>R. E.</given-names></name>
<name><surname>Smith</surname>
<given-names>R. A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1622</fpage>
<lpage>1624</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001622">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001622">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photochemistry. Part V. The illumination of some quinones in the presence of conjugated dienes and other olefinic systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001625</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Hesp</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1625</fpage>
<lpage>1635</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001625">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001625">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. Di-[5,5-dimethyl-2-oxo-1,3,2-dioxaphosphorinan-2-yl] disulphide and its deoxygenation and desulphuration with triphenylphosphine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001635</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1635</fpage>
<lpage>1637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001635">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001635">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benzo[&lt;i&gt;c&lt;/i&gt;]cinnoline: a correction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1638</fpage>
<lpage>1638</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclisation reactions involving the oxidation of carboxylic acids with lead tetra-acetate. Part I. The conversion of 2′-substituted biphenyl-2-carboxylic acids into 3,4-benzocoumarin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001639</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Waring</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1639</fpage>
<lpage>1642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001639">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001639">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sulphur monochloride on aromatic primary amines: the Herz reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hope</surname>
<given-names>P.</given-names></name>
<name><surname>Wiles</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1642</fpage>
<lpage>1644</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2-azidotropone. Part I. Thermal and photochemical transformations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001645</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hobson</surname>
<given-names>J. D.</given-names></name>
<name><surname>Malpass</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1645</fpage>
<lpage>1648</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001645">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001645">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nickel 1-alkyltetradehydrocorrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001648</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clarke</surname>
<given-names>D. A.</given-names></name>
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Harris</surname>
<given-names>R. L. N.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Kay</surname>
<given-names>I. T.</given-names></name>
<name><surname>Shelton</surname>
<given-names>K. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1648</fpage>
<lpage>1656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cinnoline synthesis. Part III. Alternative routes to 4-hydroxy-6-nitrocinnoline and 4,6-diaminocinnoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001657</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barber</surname>
<given-names>H. J.</given-names></name>
<name><surname>Lunt</surname>
<given-names>E.</given-names></name>
<name><surname>Washbourn</surname>
<given-names>K.</given-names></name>
<name><surname>Wragg</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1657</fpage>
<lpage>1664</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001657">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001657">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transaminations of &lt;i&gt;NN&lt;/i&gt;-dimethylformamide azine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001664</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartlett</surname>
<given-names>R. K.</given-names></name>
<name><surname>Humphrey</surname>
<given-names>I. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1664</fpage>
<lpage>1666</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001664">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001664">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of cytochalasins A and B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aldridge</surname>
<given-names>D. C.</given-names></name>
<name><surname>Armstrong</surname>
<given-names>J. J.</given-names></name>
<name><surname>Speake</surname>
<given-names>R. N.</given-names></name>
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1667</fpage>
<lpage>1676</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photochemistry. Part V. The photocyclodehydrogenation of 2-furyl- and 2-thienyl-ethylenes: the mass spectra of the products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001677</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Loader</surname>
<given-names>C. E.</given-names></name>
<name><surname>Timmons</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1677</fpage>
<lpage>1681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001677">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001677">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-(2-acetylaminoethyl)-6-hydroxy-5-methoxyindole (6-hydroxymelatonin)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001681</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>D. E.</given-names></name>
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1681</fpage>
<lpage>1682</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001681">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001681">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrones. Part V. The reaction of a cyclic nitrone with diethyl malonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001683</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kaminsky</surname>
<given-names>L. S.</given-names></name>
<name><surname>Lamchen</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1683</fpage>
<lpage>1685</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001683">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001683">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. Synthesis of spirilloxanthin, “OH-spirilloxanthin,” and 3,4-dehydrorhodopin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001686</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schneider</surname>
<given-names>D. F.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1686</fpage>
<lpage>1689</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001686">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001686">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 Ullmann reaction. Part I. The reaction of 2,3-di-iodonitrobenzene with copper bronze</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001690</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Iqbal</surname>
<given-names>K.</given-names></name>
<name><surname>Wilson</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1690</fpage>
<lpage>1693</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001690">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001690">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tropones. Part I. The action of alkali on 2-halogenotropones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001693</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>E. J.</given-names></name>
<name><surname>Warrell</surname>
<given-names>D. C.</given-names></name>
<name><surname>Fry</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1693</fpage>
<lpage>1696</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001693">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001693">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;-carboxy-anhydrides derived from &lt;i&gt;threo&lt;/i&gt;- and &lt;i&gt;erythro&lt;/i&gt;-β-hydroxyaspartic acids and poly-β-methyl hydrogen &lt;i&gt;threo&lt;/i&gt;-β-methoxy-DL-aspartate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001696</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Liwschitz</surname>
<given-names>Y.</given-names></name>
<name><surname>Singerman</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1696</fpage>
<lpage>1700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001696">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001696">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Phenylazocholest-5-en-3β-ol: the so-called 3β,5α-dihydroxycholestan-6-one phenylhydrazone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001700</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckingham</surname>
<given-names>J.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1700</fpage>
<lpage>1702</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001700">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001700">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Phenylazocholestane derivatives: reassignment of the structures of products from phenylhydrazine and ozonised cholesterol derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001703</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckingham</surname>
<given-names>J.</given-names></name>
<name><surname>Chittenden</surname>
<given-names>G. J. F.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1703</fpage>
<lpage>1706</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001703">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001703">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. A novel sulphur-containing bicyclic system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001706</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ashby</surname>
<given-names>J.</given-names></name>
<name><surname>Eisner</surname>
<given-names>Ulli</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1706</fpage>
<lpage>1710</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001706">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001706">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The chemistry of hydroxyperezone and perezinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001710</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Archer</surname>
<given-names>D. A.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1710</fpage>
<lpage>1716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001710">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001710">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 inhibition of enolisation in triacylmethanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nonhebel</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1716</fpage>
<lpage>1718</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001716">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some substituted pyoluteorins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001718</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elix</surname>
<given-names>J. A.</given-names></name>
<name><surname>Sargent</surname>
<given-names>M. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1718</fpage>
<lpage>1720</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001718">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001718">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. The mechanism of dehydrogenation of steroidal ketones by 2,3-dichloro-5,6-dicyanobenzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001720</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
<name><surname>Ringold</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1720</fpage>
<lpage>1730</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001720">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001720">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Extension of the Hammick reaction to 2-pyridylacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001730</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Betts</surname>
<given-names>M. J.</given-names></name>
<name><surname>Brown</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1730</fpage>
<lpage>1731</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001730">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001730">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ketohexoses. Part I. Derivatives of 5-amino-5-deoxy-D-fructose and-L-sorbose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001732</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Murphy</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1732</fpage>
<lpage>1734</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001732">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001732">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gallotannins. Part XIV. Structure of the gallotannins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001734</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haslam</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1734</fpage>
<lpage>1738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001734">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001734">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. Structure and synthesis of (–)-melanthioidine, a bisphenethylisoquinoline alkaloid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Herbert</surname>
<given-names>R. B.</given-names></name>
<name><surname>Mo</surname>
<given-names>Mrs. Lucy</given-names></name>
<name><surname>Šantavý</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1739</fpage>
<lpage>1744</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001739">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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[3,2-&lt;i&gt;d&lt;/i&gt;]pyrimidines from 5-aminopyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001745</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1745</fpage>
<lpage>1750</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001745">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001745">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-carboxy-6-nitrobenzimidazole 1-oxides by intramolecular oxidation of α-(2,4-dinitrophenylamino)-αβ-unsaturated acyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001750</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Luetzow</surname>
<given-names>A. E.</given-names></name>
<name><surname>Vercellotti</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1750</fpage>
<lpage>1758</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001750">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001750">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclodehydration: the acid-catalysed conversion of α-(4-ethoxynaphth-1-yl)benzoin into 1,2-diphenyl-5-ethoxynaphto-[2,1-&lt;i&gt;b&lt;/i&gt;]furan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001758</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clowes</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1758</fpage>
<lpage>1760</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001758">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001758">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 synthesis of methyl 4-deoxy-α-D-&lt;i&gt;xylo&lt;/i&gt;-hexopyranoside (“methyl 4-deoxy-α-D-glucoside”) 2,3,6-triacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001761</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gero</surname>
<given-names>S. D.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1761</fpage>
<lpage>1762</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001761">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001761">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 terpene and steroid hydantoins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Chisholm</surname>
<given-names>(Mrs) Mary</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1762</fpage>
<lpage>1764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photolysis of &lt;i&gt;N&lt;/i&gt;-2,4-dinitrophenylamino-acids to give 2-substituted 6-nitrobenzimidazole 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001764</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Neadle</surname>
<given-names>D. J.</given-names></name>
<name><surname>Pollitt</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1764</fpage>
<lpage>1766</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001764">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001764">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 organotin maleates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001767</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mufti</surname>
<given-names>A. S.</given-names></name>
<name><surname>Poller</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1767</fpage>
<lpage>1768</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001767">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001767">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;i&gt;O&lt;/i&gt;-alkylidene-α-D-glycopyranoses. Part I. The diastereoisomeric 1,2-&lt;i&gt;O&lt;/i&gt;-(1-methylpropylidene)-α-D-glucopyranoses</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001768</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rees</surname>
<given-names>R. G.</given-names></name>
<name><surname>Tatchell</surname>
<given-names>A. R.</given-names></name>
<name><surname>Wells</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1768</fpage>
<lpage>1772</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001768">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001768">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Cholesta-1,3,5-trien-7-one and its dimer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001773</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connolly</surname>
<given-names>J. P.</given-names></name>
<name><surname>Manning</surname>
<given-names>A. R.</given-names></name>
<name><surname>Thomson</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1773</fpage>
<lpage>1775</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001773">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001773">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 triterpenoid acid from &lt;i&gt;Lenzites trabea&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001776</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawrie</surname>
<given-names>W.</given-names></name>
<name><surname>McLean</surname>
<given-names>J.</given-names></name>
<name><surname>Watson</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1776</fpage>
<lpage>1779</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001776">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001776">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 4-allyl- and 4-benzyl-2,6-dimethylbromobenzene from 2,6-xylidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001780</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1780</fpage>
<lpage>1782</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001780">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001780">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Oxaphenalen-3(2&lt;i&gt;H&lt;/i&gt;)-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001782</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alderson</surname>
<given-names>D.</given-names></name>
<name><surname>Livingstone</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1782</fpage>
<lpage>1784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001782">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001782">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkaloid biosynthesis. Part X. Terminal Steps in the Biosynthesis of the Morphine Alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001785</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Martin</surname>
<given-names>J. A.</given-names></name>
<name><surname>Brochmann-Hanssen</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1785</fpage>
<lpage>1788</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001785">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001785">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 aliphatic diphosphonic tetrachlorides. Part II. Some reactions of diphosphonic tetrachlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001789</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kosolapoff</surname>
<given-names>Gennady M.</given-names></name>
<name><surname>Brown jun. </surname>
<given-names>Alfred D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1789</fpage>
<lpage>1791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001789">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001789">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 relationship of bisanthranil to its structural isomer and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001792</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gibson</surname>
<given-names>G. K. J.</given-names></name>
<name><surname>Lindsey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Paisley</surname>
<given-names>H. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1792</fpage>
<lpage>1795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001792">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001792">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 rotenoids. Evidence for 1,2-aryl migration and the isoflavonoid construction of rings A, C, and D in rotenone and amorphigenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001796</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Thomas</surname>
<given-names>M. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1796</fpage>
<lpage>1801</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001796">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001796">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 equilibrium between γ-lactones and alkenoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001802</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Grimwood</surname>
<given-names>B. E.</given-names></name>
<name><surname>Kafka</surname>
<given-names>T. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1802</fpage>
<lpage>1803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001802">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001802">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 formaldehyde with methylene compounds. Part I. Products from acetoacetic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Richardson</surname>
<given-names>M. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1804</fpage>
<lpage>1808</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 basic and acidic derivatives of 2,5-dihydro-1&lt;i&gt;H&lt;/i&gt;-1-benzazepine as potential therapeutic agents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001808</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1808</fpage>
<lpage>1813</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001808">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001808">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. Keto–enol tautomerism in santonene and dihydrosantonene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001813</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Mollan</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1813</fpage>
<lpage>1817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001813">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001813">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 route to 9-phenanthrylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Altiparmakian</surname>
<given-names>R. H.</given-names></name>
<name><surname>Braithwaite</surname>
<given-names>R. S. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1818</fpage>
<lpage>1818</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some 12-oxygenated derivatives of oestradiol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001819</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coombs</surname>
<given-names>M. M.</given-names></name>
<name><surname>Roderick</surname>
<given-names>H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1819</fpage>
<lpage>1821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001819">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001819">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. Nucleophilic substitution in tetrafluoropyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001822</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Field</surname>
<given-names>D. S.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1822</fpage>
<lpage>1826</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001822">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001822">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Trihalogenomethyl compounds of potential therapeutic interest. Part VII. Some selective reductions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001827</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bishop</surname>
<given-names>D. C.</given-names></name>
<name><surname>Williamson</surname>
<given-names>W. R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1827</fpage>
<lpage>1827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001827">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001827">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrazolo-&lt;i&gt;as&lt;/i&gt;-triazines. Part III. Ring fission</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001828</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Partridge</surname>
<given-names>M. W.</given-names></name>
<name><surname>Stevens</surname>
<given-names>M. F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1828</fpage>
<lpage>1830</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001828">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001828">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 methods in peptide synthesis. Part V. On α- and &lt;i&gt;γ&lt;/i&gt;-diphenylmethyl and phenacyl esters of L-glutamic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001830</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor-Papadimitriou</surname>
<given-names>J.</given-names></name>
<name><surname>Yovanidis</surname>
<given-names>C.</given-names></name>
<name><surname>Paganou</surname>
<given-names>A.</given-names></name>
<name><surname>Zervas</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1830</fpage>
<lpage>1836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001830">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001830">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>8-Azachromones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonsall</surname>
<given-names>C.</given-names></name>
<name><surname>Hill</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1836</fpage>
<lpage>1839</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXI. Spectroscopic determination of the fine structures of imines derived from lupones and agglomerone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001839</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Laws</surname>
<given-names>D. R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1839</fpage>
<lpage>1842</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001839">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001839">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ferrocene derivatives. Part XVI. The aminomethylation of methylthio- and bismethylthio-ferrocene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001842</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knox</surname>
<given-names>G. R.</given-names></name>
<name><surname>Morrison</surname>
<given-names>I. G.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1842</fpage>
<lpage>1847</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001842">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001842">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ferrocene derivatives. Part XVII. The aminomethylation of methoxy- and dimethoxy-ferrocene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001847</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McVey</surname>
<given-names>S.</given-names></name>
<name><surname>Morrison</surname>
<given-names>I. G.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1847</fpage>
<lpage>1850</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001847">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001847">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ferrocene derivatives. Part XVIII. The aminomethylation of methyl- and dimethyl-ferrocene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001851</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Sandhu</surname>
<given-names>M. A.</given-names></name>
<name><surname>Watts</surname>
<given-names>W. E.</given-names></name>
<name><surname>Haley</surname>
<given-names>R. C.</given-names></name>
<name><surname>Knox</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1851</fpage>
<lpage>1853</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001851">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001851">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ferrocene derivatives. Part XIX. Substitution patterns</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001853</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knox</surname>
<given-names>G. R.</given-names></name>
<name><surname>Morrison</surname>
<given-names>I. G.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Sandhu</surname>
<given-names>M. A.</given-names></name>
<name><surname>Watts</surname>
<given-names>W. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1853</fpage>
<lpage>1856</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001853">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001853">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isomerisations akin to the Dimroth rearrangement. Part II. The equilibria of 4-mercapto-1,2,3,5,7-penta-azaindenes with 4-amino-1-thia-2,3,5,7-tetra-azaindenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001856</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Paddon-Row</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1856</fpage>
<lpage>1860</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001856">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001856">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 arynes by reaction of potassium t-butoxide with aryl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001860</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Hall</surname>
<given-names>Julia K. A.</given-names></name>
<name><surname>Sharp</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1860</fpage>
<lpage>1862</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001860">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001860">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 intermediates. Part III. The reactions of cyclopropenones with iron and cobalt carbonyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001862</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bird</surname>
<given-names>C. W.</given-names></name>
<name><surname>Hollins)</surname>
<given-names>E. M. Briggs (née</given-names></name>
<name><surname>Hudec</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1862</fpage>
<lpage>1864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001862">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001862">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;i&gt;O&lt;/i&gt;-benzyl-L-glycerol and D-(glycerol 1,2-carbonate)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001865</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gigg</surname>
<given-names>Jill</given-names></name>
<name><surname>Gigg</surname>
<given-names>Roy</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1865</fpage>
<lpage>1866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001865">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001865">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stable pyridine anhydro-bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001866</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Ezekiel</surname>
<given-names>A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1866</fpage>
<lpage>1868</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001866">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001866">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2,2′-biphenylylenebisdiethylphosphine. Formation of cyclic diquaternary dibromides with alkylene dibromides, and the nature and probable mechanism of their thermal decomposition</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001869</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>David W.</given-names></name>
<name><surname>Millar</surname>
<given-names>Ian T.</given-names></name>
<name><surname>Mann</surname>
<given-names>F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1869</fpage>
<lpage>1875</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001869">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001869">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetical studies of terpenoids. Part XI. A new synthesis of methyl (±)-β-(5,5,9-trimethyl-2-oxo-&lt;i&gt;trans&lt;/i&gt;-1-decalyl)propionate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001876</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mukhopadhyay</surname>
<given-names>Sunil Kumar</given-names></name>
<name><surname>Dutta</surname>
<given-names>Phanindra Chandra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1876</fpage>
<lpage>1878</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001876">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001876">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part III. The interaction of substituted diguanides with isothiocyanate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001878</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
<name><surname>Pitchfork</surname>
<given-names>Ernest D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1878</fpage>
<lpage>1885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001878">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001878">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part IV. The interaction of diguanide and its homologues with isocyanate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001886</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
<name><surname>Pitchfork</surname>
<given-names>Ernest D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1886</fpage>
<lpage>1892</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001886">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001886">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Uroterpenol β-D-glucuronide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001893</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Price</surname>
<given-names>A. W.</given-names></name>
<name><surname>Wade</surname>
<given-names>A. P.</given-names></name>
<name><surname>Wilkinson</surname>
<given-names>G. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1893</fpage>
<lpage>1896</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001893">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001893">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzo[b]thiophen derivatives. Part V. The syntheses of 3-(2-amino-ethyl)-6-hydroxybenzo[&lt;i&gt;b&lt;/i&gt;]thiophen and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001897</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin-Smith</surname>
<given-names>M.</given-names></name>
<name><surname>Reid</surname>
<given-names>S. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1897</fpage>
<lpage>1898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001897">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001897">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzo[&lt;i&gt;b&lt;/i&gt;]thiophen derivatives. Part VI. The syntheses of 3-(2-amino-ethyl)-5-hydroxybenzo[&lt;i&gt;b&lt;/i&gt;]thiophen and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001899</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin-Smith</surname>
<given-names>M.</given-names></name>
<name><surname>Sneader</surname>
<given-names>W. E.</given-names></name>
<name><surname>Brown</surname>
<given-names>Ivor</given-names></name>
<name><surname>Reid</surname>
<given-names>S. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1899</fpage>
<lpage>1905</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001899">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001899">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 4-phenyl-1,2,4-triazoline-3,5-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001905</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Gilani</surname>
<given-names>S. S. H.</given-names></name>
<name><surname>Stevens</surname>
<given-names>I. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1905</fpage>
<lpage>1909</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001905">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001905">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydroxy-quinones. Part III. The reaction of 2,5-dihydroxy-benzoquinones with alkali</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001909</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>John F.</given-names></name>
<name><surname>Fooks</surname>
<given-names>Alan G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1909</fpage>
<lpage>1913</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001909">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001909">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 (±)-di-&lt;i&gt;O&lt;/i&gt;-methylcurvularin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001913</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>Paul M.</given-names></name>
<name><surname>Bycroft</surname>
<given-names>B. W.</given-names></name>
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1913</fpage>
<lpage>1915</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001913">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001913">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXI. A comparison of the photolysis and pyrolysis of organic nitrites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001915</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Ramsay</surname>
<given-names>G. C.</given-names></name>
<name><surname>Wege</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1915</fpage>
<lpage>1919</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001915">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001915">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 metal chelates. Part III. Steric effects of the β-diketone ligand</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001919</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nonhebel</surname>
<given-names>D. C.</given-names></name>
<name><surname>Smith</surname>
<given-names>John</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1919</fpage>
<lpage>1922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001919">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001919">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The formation and isomerisations of propynyl (and related)-iminopyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001922</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1922</fpage>
<lpage>1927</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001922">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001922">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The exceptionally slow rearrangement of 1,2-dihydro-2-imino-1,4-dimethylpyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001928</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Paddon-Row</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1928</fpage>
<lpage>1933</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001928">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001928">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 oxygen heterocycles. Part (V). The mass spectra of 2′-hydroxyflavonoids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001933</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pelter</surname>
<given-names>Andrew</given-names></name>
<name><surname>Stainton</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1933</fpage>
<lpage>1937</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001933">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001933">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The addition of dimethylketen to some 9-substituted acridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001937</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Procter</surname>
<given-names>S. A.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1937</fpage>
<lpage>1943</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001937">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001937">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 marrubiin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001943</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Appleton</surname>
<given-names>R. A.</given-names></name>
<name><surname>Fulke</surname>
<given-names>J. W. B.</given-names></name>
<name><surname>Henderson</surname>
<given-names>M. S.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1943</fpage>
<lpage>1947</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001943">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001943">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Daphnandra&lt;/i&gt; species. Part VII. Chemical evidence for the structure of repanduline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001948</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harley-Mason</surname>
<given-names>John</given-names></name>
<name><surname>Howard</surname>
<given-names>A. S.</given-names></name>
<name><surname>Taylor</surname>
<given-names>W. I.</given-names></name>
<name><surname>Vernengo</surname>
<given-names>M. J.</given-names></name>
<name><surname>Bick</surname>
<given-names>I. R. C.</given-names></name>
<name><surname>Clezy</surname>
<given-names>P. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1948</fpage>
<lpage>1951</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001948">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001948">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Daphnandra&lt;/i&gt; species. Part VIII. The structure of repanduline. The evidence based on mass spectrometry and nuclear magnetic resonance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001951</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bick</surname>
<given-names>I. R. C.</given-names></name>
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Harley-Mason</surname>
<given-names>John</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1951</fpage>
<lpage>1957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001951">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001951">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Daphnandra&lt;/i&gt; species. Part IX. Synthesis of (±)-hemirepanduline, the racemate of a degradation product of repanduline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001957</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aoki</surname>
<given-names>K.</given-names></name>
<name><surname>Harley-Mason</surname>
<given-names>John</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1957</fpage>
<lpage>1959</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001957">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001957">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cephalosporanic acids. Part V. The action of bidentate nucleophiles on cephalosporanic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001959</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fazakerley</surname>
<given-names>H.</given-names></name>
<name><surname>Gilbert</surname>
<given-names>D. A.</given-names></name>
<name><surname>Gregory</surname>
<given-names>G. I.</given-names></name>
<name><surname>Lazenby</surname>
<given-names>J. K.</given-names></name>
<name><surname>Long</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1959</fpage>
<lpage>1963</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001959">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001959">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Decomposition of toluene-&lt;i&gt;p&lt;/i&gt;-sulphonylhydrazones by alkali. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001964</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartlett</surname>
<given-names>R. K.</given-names></name>
<name><surname>Stevens</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1964</fpage>
<lpage>1968</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001964">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001964">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 revised structure for neogmelinol: determinations of configurations in tetrahydrofuranoid lignans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001968</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Macdonald</surname>
<given-names>P. L.</given-names></name>
<name><surname>Pelter</surname>
<given-names>Andrew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1968</fpage>
<lpage>1972</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001968">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001968">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsymmetrical polynuclear cinnoline derivatives. Part II. Some pentacyclic and methyl substituted tetracyclic cinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001973</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Altiparmakian</surname>
<given-names>R. H.</given-names></name>
<name><surname>Braithwaite</surname>
<given-names>R. S. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1973</fpage>
<lpage>1979</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001973">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001973">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclic tetra-amines and their metal–ion complexes. Part IV. Two isomeric 5,7,7,12,12,14-hexamethyl-1,4,8,11-tetra-azacyclotetradecanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001979</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Curtis</surname>
<given-names>N. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1979</fpage>
<lpage>1980</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001979">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001979">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The formation and trapping of the 3-methyl-1,4-naphthaquinon-2-ylmethyl carbanion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001980</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>
<name><surname>Morton</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1980</fpage>
<lpage>1984</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001980">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001980">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Multimacrocyclic compounds. Part IV. Internal trimerisation of the triple bonds of linear triynes on a Ziegler catalyst</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001984</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1984</fpage>
<lpage>1985</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001984">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001984">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dimethyl acetylenedicarboxylate with derivatives of malonic acid: pentamethoxycarbonylcyclopentadienide anion, tetramethoxy-carbonylcyclopentadienone, cyanotetramethoxyfulvenolate anion, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001986</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Henstock</surname>
<given-names>J. B.</given-names></name>
<name><surname>Hudec</surname>
<given-names>J.</given-names></name>
<name><surname>Whitear</surname>
<given-names>B. R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1986</fpage>
<lpage>1993</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001986">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001986">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 condensation products of (+)-menthofuran with carbonyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001993</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>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Pratt</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1993</fpage>
<lpage>1998</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001993">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001993">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 allylic phosphines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670001998</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Savage</surname>
<given-names>M. P.</given-names></name>
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1998</fpage>
<lpage>1999</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670001998">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670001998">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 proton magnetic resonance of some coumarins and 2,2-dimethylchromens: further examples of inter-ring spin–spin coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002000</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lassak</surname>
<given-names>E. V.</given-names></name>
<name><surname>Pinhey</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2000</fpage>
<lpage>2001</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002000">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002000">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 eburicoic acid from sesquiterpene precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002002</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawrie</surname>
<given-names>W.</given-names></name>
<name><surname>McLean</surname>
<given-names>J.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Watson</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2002</fpage>
<lpage>2004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002002">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002002">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. A generalised monocyclic rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002005</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Hamid</surname>
<given-names>A. Majid</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2005</fpage>
<lpage>2007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002005">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The free-radical addition of polyhalogenomethanes and of thiols to 2,3-dichloronorborna-2,5-diene, and the preparation of 2,3-dichloroquadricyclene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alden</surname>
<given-names>C. K.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2007</fpage>
<lpage>2011</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thiophens. Part IV. Synthesis of some 2,2′-bithienyl derivatives from cuprous acetylides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. E.</given-names></name>
<name><surname>Curtis</surname>
<given-names>R. F.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2011</fpage>
<lpage>2015</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cleavage of tertiary bases with phenyl chloroformate: the reconversion of 21-deoxyajmaline into ajmaline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hobson</surname>
<given-names>J. D.</given-names></name>
<name><surname>McCluskey</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2015</fpage>
<lpage>2017</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 ylids. Part III. Reactions with acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2018</fpage>
<lpage>2021</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;NN&lt;/i&gt;-di-(1-cyanoalkyl)hydroxylamines. Part IV. Isolation of acyclic nitrones and their reaction with hydrogen cyanide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002022</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Masui</surname>
<given-names>Masaichiro</given-names></name>
<name><surname>Yijima</surname>
<given-names>Chino</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2022</fpage>
<lpage>2023</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002022">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002022">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and related natural products. Part XLI. 14α-Methyl oestranes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002024</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pettit</surname>
<given-names>George R.</given-names></name>
<name><surname>Brown</surname>
<given-names>Thomas H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2024</fpage>
<lpage>2026</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002024">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002024">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Diazoindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moss</surname>
<given-names>Robert A.</given-names></name>
<name><surname>Funk</surname>
<given-names>Joel D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2026</fpage>
<lpage>2027</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystalline modifications of salicylidenaminoguanidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002027</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>M. D.</given-names></name>
<name><surname>Spedding</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2027</fpage>
<lpage>2028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002027">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002027">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;i&gt;O&lt;/i&gt;-Ethylenepentopyranoses</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002028</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Inglis</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2028</fpage>
<lpage>2030</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 co-ordinated ligands. Part III. Reactions of Schiff bases co-ordinated with magnesium. A preparation of 3-aminocoumarin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Houghton</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2030</fpage>
<lpage>2032</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 addition of alcohols to the double bond in Δ&lt;sup&gt;16&lt;/sup&gt;-20-oxo-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bladon</surname>
<given-names>Peter</given-names></name>
<name><surname>Williams</surname>
<given-names>Ivor A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2032</fpage>
<lpage>2037</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vapour pressures, heats of sublimation, and heats of vaporisation for straight-chain ethyl esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002038</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Omar</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2038</fpage>
<lpage>2040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002038">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002038">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2,3-disubstituted chromones: cyclisation of the enolesters of &lt;i&gt;o&lt;/i&gt;-acyloxyphenyl alkyl ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Széll</surname>
<given-names>Thomas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2041</fpage>
<lpage>2044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Stepwise synthesis of porphyrins through &lt;i&gt;a&lt;/i&gt;-oxo-bilanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002045</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>Sach</surname>
<given-names>G. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2045</fpage>
<lpage>2059</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;o&lt;/i&gt;-cyanocinnamonitriles and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002059</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2059</fpage>
<lpage>2066</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002059">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002059">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVIII. The synthesis of phenanthridinium-5-vinyloxides and pyrrolo[1,2-&lt;i&gt;f&lt;/i&gt;]phenanthridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002066</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Selby</surname>
<given-names>I. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2066</fpage>
<lpage>2071</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002066">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002066">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rearrangements of diphenylamine derivatives. Part I. The rearrangement of &lt;i&gt;N&lt;/i&gt;-benzoyldiphenylamine and some related acylation reations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002071</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birchall</surname>
<given-names>J. M.</given-names></name>
<name><surname>Thorpe</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2071</fpage>
<lpage>2076</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002071">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002071">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;N&lt;/i&gt;-aryl-4-t-butylcyclohexylamines &lt;i&gt;via&lt;/i&gt; anils</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002077</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bull</surname>
<given-names>J. R.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. G.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Richards</surname>
<given-names>(Mrs) E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2077</fpage>
<lpage>2081</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002077">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002077">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 steroids. Part I. The preparation of 3β, 16α-dihydroxyandrost-5-ene-11,17-dione and 3β,11β,16α-trihydroxyandrost-5-en-17-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002082</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kelly</surname>
<given-names>R. W.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2082</fpage>
<lpage>2084</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002082">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002082">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 properties of some 3-acetyl- and 3-formyl-5-halogenobenzo[&lt;i&gt;b&lt;/i&gt;]thiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shanta</surname>
<given-names>M. S. El</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2084</fpage>
<lpage>2089</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. Synthesis and some reactions of 2,3,5,6-tetrafluoropyridine-4-aldehyde and -4-nitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002089</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>Young</surname>
<given-names>I. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2089</fpage>
<lpage>2091</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002089">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002089">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Synthesis and some reactions of 2,3,5,6-tetrafluoro-4-iodopyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002091</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>Phillips</surname>
<given-names>E.</given-names></name>
<name><surname>Young</surname>
<given-names>I. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2091</fpage>
<lpage>2095</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 micrococcin &lt;i&gt;P&lt;/i&gt;. Part XI. Application of a simple micromethod for the identification of lower volatile fatty acids to the structural study of 2-acylthiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002095</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>M.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2095</fpage>
<lpage>2096</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002095">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002095">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biphenylenes: the synthesis of 1-nitro- and 1-amino-biphenylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002097</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>J. W.</given-names></name>
<name><surname>Whitaker</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2097</fpage>
<lpage>2099</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002097">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002097">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The quinonoid constituents of &lt;i&gt;Tabebuia avellanedae&lt;/i&gt;(Bignoniaceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002100</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burnett</surname>
<given-names>A. R.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2100</fpage>
<lpage>2104</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002100">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002100">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of &lt;i&gt;N&lt;/i&gt;-benzyl-&lt;i&gt;threo&lt;/i&gt;-β-hydroxy-DL-aspartic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002104</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Liwschitz</surname>
<given-names>Y.</given-names></name>
<name><surname>Edlitz-Pfeffermann</surname>
<given-names>Yolan</given-names></name>
<name><surname>Singerman</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2104</fpage>
<lpage>2105</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002104">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002104">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benzotrifurazan and of some complexes which it forms with organic molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002105</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Evans</surname>
<given-names>Miss J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2105</fpage>
<lpage>2109</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002105">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002105">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 decomposition of some β-azido-carbonyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002109</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>A. J.</given-names></name>
<name><surname>Donald</surname>
<given-names>A. S. R.</given-names></name>
<name><surname>Marks</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2109</fpage>
<lpage>2112</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002109">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002109">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benz[&lt;i&gt;de&lt;/i&gt;]anthracene derivatives and related systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002113</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Kingston</surname>
<given-names>D. G. I.</given-names></name>
<name><surname>Schütz</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2113</fpage>
<lpage>2118</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002113">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002113">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 halogenated derivatives of 2,6-dihydroxyanthracene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002118</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Schütz</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2118</fpage>
<lpage>2120</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002118">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002118">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and reduction of some methoxy-anthracenes and their derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002121</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Schütz</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2121</fpage>
<lpage>2125</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002121">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002121">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and reduction of 5-hydroxy-2-methylnaphtho[1,2-&lt;i&gt;b&lt;/i&gt;]furan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002126</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Hildyard</surname>
<given-names>E. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2126</fpage>
<lpage>2128</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002126">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002126">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrones. Part VI. The pyrolysis of oxaziridines derived by photolysis of cyclic nitrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kaminsky</surname>
<given-names>L. S.</given-names></name>
<name><surname>Lamchen</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2128</fpage>
<lpage>2130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 trivalent phosphorus compounds by disulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002131</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2131</fpage>
<lpage>2134</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and biosynthesis. Part XV. The biosynthesis of roemerine, anonaine, and mecambrine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002134</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Bhakuni</surname>
<given-names>D. S.</given-names></name>
<name><surname>Chapman</surname>
<given-names>G. M.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2134</fpage>
<lpage>2140</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002134">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002134">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peptide cyclisations: the use of bis-&lt;i&gt;o&lt;/i&gt;-phenylene pyrophosphite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002140</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>A. W.</given-names></name>
<name><surname>Smith</surname>
<given-names>P. W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2140</fpage>
<lpage>2144</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002140">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002140">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Taxine. Part VII. The stereochemistry of hydrogenolysis of &lt;i&gt;O&lt;/i&gt;-β-phenylpropionyltaxicin-I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002144</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dukes</surname>
<given-names>M.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2144</fpage>
<lpage>2147</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002144">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002144">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 3,3-diethylpiperid-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002148</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>J. A.</given-names></name>
<name><surname>Harper</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2148</fpage>
<lpage>2148</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002148">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002148">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 method for the catalytic partial hydrogenation of diolefins to mono-olefins. Preparation of cycloalkenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002149</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2149</fpage>
<lpage>2152</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002149">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002149">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-2,3-dihydroxybenzoquinone dimer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002152</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>H. A.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2152</fpage>
<lpage>2155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002152">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002152">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Zanthoxylum caribaeum&lt;/i&gt; Lam</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002155</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casa</surname>
<given-names>Deanna Della</given-names></name>
<name><surname>C</surname>
<given-names>María Sojo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2155</fpage>
<lpage>2156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002155">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002155">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Butadiene sulphone chemistry. Part I. Addition reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Argyle</surname>
<given-names>C. S.</given-names></name>
<name><surname>Goadby</surname>
<given-names>S. C.</given-names></name>
<name><surname>Mason</surname>
<given-names>K. G.</given-names></name>
<name><surname>Reed</surname>
<given-names>R. A.</given-names></name>
<name><surname>Smith</surname>
<given-names>M. A.</given-names></name>
<name><surname>Stern</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2156</fpage>
<lpage>2170</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Butadiene sulphone chemistry. Part II. 3-Oxotetrahydrothiophen dioxide and its reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002171</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mason</surname>
<given-names>K. G.</given-names></name>
<name><surname>Smith</surname>
<given-names>M. A.</given-names></name>
<name><surname>Stern</surname>
<given-names>E. S.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2171</fpage>
<lpage>2176</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Butadiene sulphone chemistry. Part III. Condensation reactions of butadiene sulphone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002176</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Argyle</surname>
<given-names>C. S.</given-names></name>
<name><surname>Mason</surname>
<given-names>K. G.</given-names></name>
<name><surname>Smith</surname>
<given-names>M. A.</given-names></name>
<name><surname>Stern</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2176</fpage>
<lpage>2180</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002176">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002176">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 recemic &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-forms of 2-cyclohexylcyclohexaneacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002180</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robins</surname>
<given-names>P. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2180</fpage>
<lpage>2182</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002180">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002180">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 (±)-glaziovine and (±)-pronuciferine by phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Yagi</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2182</fpage>
<lpage>2184</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroaryl organometallic compounds. Part IV. Fluorocarbon derivatives of tricovalent aluminium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002185</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Cunningham</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2185</fpage>
<lpage>2188</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002185">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002185">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 compounds. Part XLI. The reaction of bis(trimethylsilyl)mercury with some ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002188</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Jackson</surname>
<given-names>R. A.</given-names></name>
<name><surname>Walsingham</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2188</fpage>
<lpage>2191</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002188">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002188">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bipyridylium quaternary salts and related compounds. Part II. The preparation of the 1,1′-diamino-4,4′-bipyridylium dication and its behaviour in alkaline solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002192</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Downes</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2192</fpage>
<lpage>2193</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002192">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002192">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>8-Hydroxy-1-naphthoyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002194</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Packer</surname>
<given-names>R. J.</given-names></name>
<name><surname>Smith</surname>
<given-names>D. C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2194</fpage>
<lpage>2201</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002194">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002194">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ginkgolides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002201</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Okabe</surname>
<given-names>K.</given-names></name>
<name><surname>Yamada</surname>
<given-names>K.</given-names></name>
<name><surname>Yamamura</surname>
<given-names>S.</given-names></name>
<name><surname>Takad</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2201</fpage>
<lpage>2206</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002201">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002201">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 fluorine compounds. Part XXXIX. Reactions of α-fluoro-β-keto-esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002206</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernest D.</given-names></name>
<name><surname>Shahak</surname>
<given-names>Israel</given-names></name>
<name><surname>Gruenwald</surname>
<given-names>Izchak</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2206</fpage>
<lpage>2207</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002206">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002206">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. Total syntheses of (±)-cryptaustoline and (±)-cryptowoline by the benzyne reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002208</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Ogasawara</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2208</fpage>
<lpage>2212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002208">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002208">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diaminobenzobisthiazoles and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002212</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2212</fpage>
<lpage>2220</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002212">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002212">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aminoalkylation of metal derivatives of indole. Part II. Coupling of indolylmagnesium iodides with halogenoalkylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002220</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ganellin</surname>
<given-names>C. R.</given-names></name>
<name><surname>Hollyman</surname>
<given-names>D. R.</given-names></name>
<name><surname>Ridley</surname>
<given-names>H. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2220</fpage>
<lpage>2225</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002220">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002220">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1-amino-2-nitrocyclopentanecarboxylic acid during acetylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2225</fpage>
<lpage>2228</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 structure determination of (+)-diaeudesmin, the first naturally occurring diaxially substituted 3,7-dioxabicyclo[3,3,0]octane lignan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002228</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atal</surname>
<given-names>C. K.</given-names></name>
<name><surname>Dhar</surname>
<given-names>K. L.</given-names></name>
<name><surname>Pelter</surname>
<given-names>Andrew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2228</fpage>
<lpage>2230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002228">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002228">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chlorinations with diphenyl sulphoxide and acid chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nagai</surname>
<given-names>U.</given-names></name>
<name><surname>Sammes</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2230</fpage>
<lpage>2232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 mass spectra of organic compounds. Part III. Synthesis and mass spectrum of 4-methylfuro(3′,2′ :3,4)coumarin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002232</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Goodchild</surname>
<given-names>J.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2232</fpage>
<lpage>2233</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002232">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002232">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 mass spectra of organic compounds. Part IV. Cyclopentane monoterpenes of the iridoid group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002234</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>T. W.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2234</fpage>
<lpage>2240</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002234">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002234">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Pyruvoylaminobenzamide, a metabolite of &lt;i&gt;Penicillium chrysogenum&lt;/i&gt; and &lt;i&gt;P. notatum&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002240</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Suter</surname>
<given-names>P. J.</given-names></name>
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2240</fpage>
<lpage>2242</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002240">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002240">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 metabolite of &lt;i&gt;Aspergillus melleus&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002242</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mills</surname>
<given-names>S. D.</given-names></name>
<name><surname>Turner</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2242</fpage>
<lpage>2244</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002242">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002242">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The addition of thiols and bromotrichloromethane to 1,2,3,4-tetrachloro-7,7-dimethoxynorborna-2,5-diene and the preparation of 1,2,3,4-tetrachloro-7,7-dimethoxyquadricyclene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002245</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2245</fpage>
<lpage>2249</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The addition of ethanethiol and thiophenol to 1,2,3,4-tetrachloronorborna-2,5-diene, 1,2,3,4,7-&lt;i&gt;syn&lt;/i&gt;-pentachloronorborna-2,5-diene, and 1,2,3,4,7-&lt;i&gt;anti&lt;/i&gt;-pentachloronorborna-2,5-diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002249</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2249</fpage>
<lpage>2254</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrocarbon–metal nitrosyls. Part II. Acyl derivatives of tricarbonylnitrosyliron, and their reactions with dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002255</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chaudhari</surname>
<given-names>F. M.</given-names></name>
<name><surname>Knox</surname>
<given-names>G. R.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2255</fpage>
<lpage>2260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002255">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002255">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. The preparation of allenic and acetylenic bromides by the triphenylphosphite dibromide method</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002260</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Black</surname>
<given-names>D. K.</given-names></name>
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Patel</surname>
<given-names>A. N.</given-names></name>
<name><surname>Whiter</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2260</fpage>
<lpage>2262</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002260">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002260">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>South African plant extractives. Part I. An alkaloid, tecleanine, from the family rutaceae</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wright</surname>
<given-names>Winifred G.</given-names></name>
<name><surname>Pegel</surname>
<given-names>K. H.</given-names></name>
<name><surname>Brown</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2262</fpage>
<lpage>2262</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Thermal reactions of perfluoro(tetrahydro-2-methyl-2&lt;i&gt;H&lt;/i&gt;-1,2-oxazine) and perfluoro-(3,6-dihydro-2-methyl-2&lt;i&gt;H&lt;/i&gt;-1,2-oxazine) : synthesis and properties of perfluoro-(1-methyl-2-pyrrolidone), perfluoro-(1-methyl-2-oxo-3-pyrroline), and perfluoro-(1-methylazetidine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002263</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>Matthews</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2263</fpage>
<lpage>2267</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002263">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002263">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrogen-containing carbohydrate derivatives. Part XVI. Re-investigation of the ‘mutarotation’ of 3,4,5,6-tetra-&lt;i&gt;O&lt;/i&gt;-benzoyl-D-glucose phenylhydrazone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002268</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckingham</surname>
<given-names>J.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2268</fpage>
<lpage>2268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 configuration of some decalin spiro-hydantoins and amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Chisholm</surname>
<given-names>(Mrs) Mary</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2269</fpage>
<lpage>2273</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 synthetic approach to 3,4-benzophenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002273</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burditt</surname>
<given-names>N. A.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
<name><surname>Venanzi</surname>
<given-names>L. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2273</fpage>
<lpage>2275</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002273">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002273">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 removal from benzene with aluminium chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>David H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2275</fpage>
<lpage>2281</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and pesticidal activities of derivatives of dinitro-phenols. Part IV. Preparation of certain 2-(α-branched alkyl)-4,6-dinitro- and 4-(α-branched alkyl)-2,6-dinitro-phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002281</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pianka</surname>
<given-names>M.</given-names></name>
<name><surname>Edwards</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2281</fpage>
<lpage>2290</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002281">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002281">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and pesticidal activities of derivatives of dinitrophenols. Part V. Reactions of certain dinitro-aryl thiocarbamates with potassium hydroxide in methanol and with various nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002290</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pianka</surname>
<given-names>M.</given-names></name>
<name><surname>Edwards</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2290</fpage>
<lpage>2295</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002290">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002290">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 alginic acid. Part VI. Minor features and structural variations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002295</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rees</surname>
<given-names>D. A.</given-names></name>
<name><surname>Samuel</surname>
<given-names>J. W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2295</fpage>
<lpage>2298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002295">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002295">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvent effects in the nuclear magnetic resonance spectra of steroidal ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002298</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glotter</surname>
<given-names>E.</given-names></name>
<name><surname>Lavie</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2298</fpage>
<lpage>2302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aqueous hydrolysis of perfluoro-αω-bisazomethines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002302</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2302</fpage>
<lpage>2305</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>7,12-Dihydropleiadene-7,12-dione: preparation and reaction with grignard reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>D. C. C.</given-names></name>
<name><surname>Steere</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2305</fpage>
<lpage>2307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The mechanism of the reaction between β-amino-ketones and thiophenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002307</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrisano</surname>
<given-names>R.</given-names></name>
<name><surname>Angeloni</surname>
<given-names>A. S.</given-names></name>
<name><surname>Maria</surname>
<given-names>P. De</given-names></name>
<name><surname>Tramontini</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2307</fpage>
<lpage>2311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002307">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002307">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 chemical effects of γ-radiation on organic systems. Part XIII. The system diethylamine–iodobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cunanan</surname>
<given-names>Miss S. A.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2311</fpage>
<lpage>2312</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organomercury compounds. Part V. Preparations of pentachlorophenylmercury compounds by decarboxylation reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002313</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deacon</surname>
<given-names>G. B.</given-names></name>
<name><surname>Felder</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2313</fpage>
<lpage>2314</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 products of 1-ethoxyvinyl esters of keto-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>D.</given-names></name>
<name><surname>Pattenden</surname>
<given-names>G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2314</fpage>
<lpage>2316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. Further observations on the influence of an &lt;i&gt;o&lt;/i&gt;-methoxy-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002316</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
<name><surname>Middleton</surname>
<given-names>B. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2316</fpage>
<lpage>2321</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002316">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002316">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 scission of cyclic acetals. Part III. Reaction of acetyl trifluoroacetate with 1,3:2,5:4,6-tri-&lt;i&gt;O&lt;/i&gt;-methylene-D-mannitol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002321</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>Bourne</surname>
<given-names>E. J.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2321</fpage>
<lpage>2326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002321">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002321">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 furan chemistry. Part V. The Diels–Alder adducts of 2,2′-bifuryl and dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Roffey</surname>
<given-names>Patrick</given-names></name>
<name><surname>Sargent</surname>
<given-names>M. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2327</fpage>
<lpage>2327</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some 1,3-benzodioxans and a revised structure for averufin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002328</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roffey</surname>
<given-names>Patrick</given-names></name>
<name><surname>Sargent</surname>
<given-names>M. V.</given-names></name>
<name><surname>Knight</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2328</fpage>
<lpage>2331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002328">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002328">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of 1-trifluoromethylethanol. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002332</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>J. W. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2332</fpage>
<lpage>2333</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 re-examination of the synthesis of perfluoro-γ-butyrolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002333</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Mullen</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2333</fpage>
<lpage>2335</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002333">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002333">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 calabash curare and &lt;i&gt;Strychnos&lt;/i&gt; species. Part IV. Caracurine-II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002335</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Hodson</surname>
<given-names>H. F.</given-names></name>
<name><surname>Rao</surname>
<given-names>G. V.</given-names></name>
<name><surname>Yeowell</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2335</fpage>
<lpage>2339</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002335">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002335">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazepines. Part VI. Condensation products from benzoylacetone and ethylenediamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002340</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gorringe</surname>
<given-names>Anita M.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
<name><surname>Marshall</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2340</fpage>
<lpage>2341</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002340">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002340">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1,4-diazabicyclo[4,3,0]nonane-2,5,9-triones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002341</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harnden</surname>
<given-names>Michael R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2341</fpage>
<lpage>2351</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002341">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002341">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 mass spectra of organic compounds. Part V. Some phenazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holliman</surname>
<given-names>F. G.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Millard</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2351</fpage>
<lpage>2356</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 comparison of the reduction of alginic acid by different methods</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002357</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Manning</surname>
<given-names>James H.</given-names></name>
<name><surname>Green</surname>
<given-names>John W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2357</fpage>
<lpage>2363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002357">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002357">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 3-acetamido-2-nitrobenzo[&lt;i&gt;b&lt;/i&gt;]thiophen and its 5-chloro- and 5-bromo- derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shanta</surname>
<given-names>M. S. El</given-names></name>
<name><surname>Scrowston</surname>
<given-names>R. M.</given-names></name>
<name><surname>Twigg</surname>
<given-names>M. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2364</fpage>
<lpage>2368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002364">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. A partial asymmetric synthesis of orixine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowman</surname>
<given-names>R. M.</given-names></name>
<name><surname>Grundon</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2368</fpage>
<lpage>2371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002368">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. The use of 1-piperidyl esters in peptide synthesis: further studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. H.</given-names></name>
<name><surname>Liberek</surname>
<given-names>B.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2371</fpage>
<lpage>2374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Methyl-5-nitrobenzaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002374</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beech</surname>
<given-names>W. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2374</fpage>
<lpage>2375</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002374">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002374">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 steroids. Part II. The deconjugation of Δ&lt;sup&gt;4&lt;/sup&gt;-3-oxo-steroids. An improved method for the preparation of 3β-hydroxyandrost-5-ene-11,17-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kelly</surname>
<given-names>R. W.</given-names></name>
<name><surname>McClenaghan</surname>
<given-names>I.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2375</fpage>
<lpage>2381</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gallotannis. Part XV. Some observations on the structure of chebulinic acid and its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002381</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haslam</surname>
<given-names>E.</given-names></name>
<name><surname>Uddin</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2381</fpage>
<lpage>2384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002381">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002381">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and Walden inversion. Part LXI. Chlorination of 5α-cholestan-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Sharma</surname>
<given-names>S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2385</fpage>
<lpage>2391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Pyrido[1,2-&lt;i&gt;a&lt;/i&gt;]pyrazin-5-ium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002391</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glover</surname>
<given-names>E. E.</given-names></name>
<name><surname>Loadman</surname>
<given-names>M. J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2391</fpage>
<lpage>2395</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002391">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002391">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 alkyl 1,1,2,2-tetrafluoroethyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002395</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>J. W. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2395</fpage>
<lpage>2396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002395">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002395">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 steroidal components of domestic plants. Part LIII. Structure of diotigenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ogata</surname>
<given-names>M.</given-names></name>
<name><surname>Yasuda</surname>
<given-names>F.</given-names></name>
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2397</fpage>
<lpage>2400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 synthesis of bisthiosemicarbazones of pentane-2,4-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002400</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Callaghan</surname>
<given-names>C. N.</given-names></name>
<name><surname>Twomey</surname>
<given-names>Dermot</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2400</fpage>
<lpage>2402</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002400">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002400">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benzofuran from the seeds of &lt;i&gt;Styrax officinalis&lt;/i&gt; L.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002402</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Segal</surname>
<given-names>Ruth</given-names></name>
<name><surname>Milo-Goldzweig</surname>
<given-names>Ilana</given-names></name>
<name><surname>Sokoloff</surname>
<given-names>Simone</given-names></name>
<name><surname>Zaitschek</surname>
<given-names>D. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2402</fpage>
<lpage>2404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002402">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002402">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the cyclohexane-1,2-diols and methyl 4,6-&lt;i&gt;O&lt;/i&gt;-benzylidene-α-D-gluco- and galacto-pyranoside with methylene halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Jones</surname>
<given-names>(the late) B. D.</given-names></name>
<name><surname>Willard</surname>
<given-names>J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2404</fpage>
<lpage>2407</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydroxy-quinones. Part IV. The reaction of 2,6-dihydroxy-benzoquinones with alkali</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002408</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbett</surname>
<given-names>John F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2408</fpage>
<lpage>2410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002408">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002408">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Syntheses of human gastrin (HI)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2410</fpage>
<lpage>2421</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fluorocarbohydrates. Part XVII. Formation of 2,5-anhydro-1-deoxy-1,1-difluoro-D-mannitol by fluorination of acetylated glucals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002422</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wood</surname>
<given-names>K. R.</given-names></name>
<name><surname>Kent</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2422</fpage>
<lpage>2425</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002422">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002422">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenylhydrazine derivatives of sugars. Part I. Evidence for the cyclic structures of some sugar phenylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002425</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blair</surname>
<given-names>H. S.</given-names></name>
<name><surname>Roberts</surname>
<given-names>G. A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2425</fpage>
<lpage>2427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002425">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002425">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and related natural products. Part XLII. 14α-Methyl cholestanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002427</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knight</surname>
<given-names>John C.</given-names></name>
<name><surname>Belletire</surname>
<given-names>John L.</given-names></name>
<name><surname>Pettit</surname>
<given-names>George R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2427</fpage>
<lpage>2432</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002427">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002427">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 t-butyl peroxide with toluene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002432</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huang</surname>
<given-names>H. H.</given-names></name>
<name><surname>Lim</surname>
<given-names>P. K. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2432</fpage>
<lpage>2436</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002432">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002432">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitration of some 2,3-dihydro-1,4-diazepinium perchlorates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002436</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnett</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2436</fpage>
<lpage>2437</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002436">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002436">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 studies of nucleic acids on polymer supports. Part I. Oligodeoxyribonucleotide synthesis on an insoluble polymer support</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002438</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackburn</surname>
<given-names>G. M.</given-names></name>
<name><surname>Brown</surname>
<given-names>M. J.</given-names></name>
<name><surname>Harris</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2438</fpage>
<lpage>2442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002438">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002438">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. A stable 1,2-diphosphorane. Restricted rotation in a stable alkylidene diphosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002442</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>M. A.</given-names></name>
<name><surname>Tebby</surname>
<given-names>J. C.</given-names></name>
<name><surname>Ward</surname>
<given-names>R. S.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2442</fpage>
<lpage>2446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002442">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002442">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Catalytic hydrogenation of some derivatives of 2-nitrophenylpyruvic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>I.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2446</fpage>
<lpage>2449</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part XLVIII. Some 3,3-diarylprop-1-enes and related quinones: the absolute configuration of latifolin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002450</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Donnelly</surname>
<given-names>D. M. X.</given-names></name>
<name><surname>Nangle</surname>
<given-names>B. J.</given-names></name>
<name><surname>Hulbert</surname>
<given-names>P. B.</given-names></name>
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Swan</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2450</fpage>
<lpage>2452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002450">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002450">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and isomerisation of α-benzyl-α′-benzylidenesuccinic acid and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heller</surname>
<given-names>H. G.</given-names></name>
<name><surname>Swinney</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2452</fpage>
<lpage>2456</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Overcrowded molecules. Part III. The synthesis and photorearrangement reactions of 2,3-bisdiphenylmethylene-1-indanone and 4&lt;i&gt;b&lt;/i&gt;,5-dihydro-5,5,10-triphenyl-11-diphenylmethylene-11&lt;i&gt;H&lt;/i&gt;-benzo[&lt;i&gt;b&lt;/i&gt;]fluorene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002457</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heller</surname>
<given-names>H. G.</given-names></name>
<name><surname>Auld</surname>
<given-names>D.</given-names></name>
<name><surname>Salisbury</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2457</fpage>
<lpage>2459</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002457">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002457">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereochemistry. Part XIX. Directive effects of remote substituents on the alkaline epoxidation of 3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002459</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2459</fpage>
<lpage>2465</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002459">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002459">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereochemistry. Part XX. The formation of 5-cyano-3-ketones from 3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002465</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2465</fpage>
<lpage>2466</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002465">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002465">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereochemistry. Part XXI. Hydrogenation of 3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-steroids over a palladium–calcium carbonate catalyst</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002467</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Combe</surname>
<given-names>Miss M. G.</given-names></name>
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2467</fpage>
<lpage>2469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002467">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002467">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereochemistry. Part XXII. Epoxidation and hydrogenation of 4-methyl-3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
<name><surname>Malunowicz</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2469</fpage>
<lpage>2471</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydrazine hydrate on isodithiobiurets</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002471</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>John S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2471</fpage>
<lpage>2472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002471">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002471">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Useful reactions of nucleophiles with some methylsulphonyl derivatives of nitrogen heterocycles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002473</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Brown</surname>
<given-names>W. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2473</fpage>
<lpage>2476</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002473">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002473">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 unsaturated acid halides. Part II. Aluminium chloride-catalysed reactions of phenylpropioloyl chloride with anisole, toluene, and naphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002476</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnston</surname>
<given-names>K. M.</given-names></name>
<name><surname>Shotter</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2476</fpage>
<lpage>2478</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002476">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002476">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Structural relationships of alkaloids of Demerara greenheart</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002479</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>K. C.</given-names></name>
<name><surname>Evans</surname>
<given-names>M. T. A.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Sangster</surname>
<given-names>A. M. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2479</fpage>
<lpage>2488</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002479">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002479">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some 4-hydroxy- and 4-methoxy-naphthylalanines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002488</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ablewhite</surname>
<given-names>A. J.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2488</fpage>
<lpage>2491</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002488">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002488">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 carrageenan system of &lt;i&gt;Gigartina skottsbergii&lt;/i&gt; S. et G. Part II. Analysis of the system and studies on the structure of the fraction precipitated at 0·3–0·4M-potassium chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002491</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cerezo</surname>
<given-names>Alberto S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2491</fpage>
<lpage>2495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002491">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002491">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclopropanes from αβ-unsaturated esters by the dimethylsulphoxonium methylide reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002495</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Punja</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2495</fpage>
<lpage>2500</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002495">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002495">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The isolation and structure of seven xanthones from &lt;i&gt;Calophyllum scriblitifolium&lt;/i&gt; Henderson and Wyatt-Smith</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002500</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2500</fpage>
<lpage>2507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002500">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002500">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 formazans from &lt;i&gt;ortho&lt;/i&gt;-substitued arylidene arylhydrazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hegarty</surname>
<given-names>A. F.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2507</fpage>
<lpage>2508</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hormones. Part XIX. (+)-9β-Androstenedione and ‘retro’-androstenedione from 9β-oestrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Rao</surname>
<given-names>G. S. R. Subba</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2509</fpage>
<lpage>2510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-2-hydroxybenzo[&lt;i&gt;b&lt;/i&gt;]furan-3-one, the cyclic hemiacetal of 2-hydroxyphenylglyoxal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002510</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howe</surname>
<given-names>R.</given-names></name>
<name><surname>Rao</surname>
<given-names>B. S.</given-names></name>
<name><surname>Heyneker</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2510</fpage>
<lpage>2514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002510">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002510">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;cis&lt;/i&gt;- into &lt;i&gt;trans&lt;/i&gt;-abienol: some reactions with mercuric acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mills</surname>
<given-names>John S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2514</fpage>
<lpage>2520</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peptides. Part XXV. The structure and synthesis of human gastrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002520</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beacham</surname>
<given-names>J.</given-names></name>
<name><surname>Bentley</surname>
<given-names>P. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>MacLeod</surname>
<given-names>J. K.</given-names></name>
<name><surname>Mendive</surname>
<given-names>J. J.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2520</fpage>
<lpage>2529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002520">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002520">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Ring a intermediates for the synthesis of tachysterol&lt;sub&gt;3&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bruck</surname>
<given-names>P. R.</given-names></name>
<name><surname>Clark</surname>
<given-names>R. D.</given-names></name>
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Günther</surname>
<given-names>W. H. H.</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2529</fpage>
<lpage>2533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The synthesis of tachysterol&lt;sub&gt;3&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002534</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Waddington-Feather</surname>
<given-names>Sheila M.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2534</fpage>
<lpage>2536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002534">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002534">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XX. Synthesis and reactions of 1,2-disubstituted benzimidazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garner</surname>
<given-names>R.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2536</fpage>
<lpage>2540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sorbifolin, a chromone from &lt;i&gt;Spathelia sorbifolia&lt;/i&gt; L.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002540</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>Willis</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2540</fpage>
<lpage>2542</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 organophosphorus compounds. Part XXII. Preparation of diethyl trichloromethylphosphonite and diethyl dichloromethylphosphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002542</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. E.</given-names></name>
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Dyson</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2542</fpage>
<lpage>2543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002542">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002542">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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′-bi-indenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002544</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kemp</surname>
<given-names>W.</given-names></name>
<name><surname>Spanswick</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2544</fpage>
<lpage>2545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002544">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002544">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of &lt;i&gt;Mammea americana&lt;/i&gt; L. Part I. The 4-n-alkylcoumarins. Isolation and structure of mammea B/BA, B/BB, B/BC, and C/BB</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002545</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>McCormick</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2545</fpage>
<lpage>2552</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of &lt;i&gt;Mammea americana&lt;/i&gt; L. Part II. The 4-phenylcoumarins. Isolation and structure of Mammea A/AA, A/A cyclo D, A/BA, A/AB, and A/BB</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002553</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>McCormick</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2553</fpage>
<lpage>2559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002553">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002553">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The reaction of bis(trimethylsilyl)mercury with aryl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002559</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>Hutton</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2559</fpage>
<lpage>2562</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002559">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002559">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thiazolopyridines and bisthiazolopyridines. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002562</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>J. A.</given-names></name>
<name><surname>Hill</surname>
<given-names>S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2562</fpage>
<lpage>2565</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002562">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002562">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Base-catalysed reactions of glyoxal. Part III. 1,2-Bis-(2-oxoimidazolidin-1-yl)ethane-1,2-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dinwoodie</surname>
<given-names>A. H.</given-names></name>
<name><surname>Fort</surname>
<given-names>G.</given-names></name>
<name><surname>Thompson</surname>
<given-names>J. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2565</fpage>
<lpage>2568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 mononitrophloroglucinol methyl ethers and benzenesulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002568</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2568</fpage>
<lpage>2570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002568">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002568">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nalgiolaxin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002570</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Stapleford</surname>
<given-names>K. S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2570</fpage>
<lpage>2571</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002570">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002570">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-(2-Naphthyl)benzo[&lt;i&gt;b&lt;/i&gt;]thiophen. Part II. Halides, and the keto-sulphone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002571</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lamberton</surname>
<given-names>Alex. H.</given-names></name>
<name><surname>Thorpe</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2571</fpage>
<lpage>2574</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002571">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002571">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Negligible steric retardation by the carboxy-group in the racemisation of 8′-methyl-1,1′-binaphthyl-8-carboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002575</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>Margaret M.</given-names></name>
<name><surname>Mazengo</surname>
<given-names>R. Z.</given-names></name>
<name><surname>Cooke</surname>
<given-names>Ann S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2575</fpage>
<lpage>2577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002575">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002575">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 trimethylamine–benzimide and related compounds: identification of by-products and their probable mechanism of formation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gibson</surname>
<given-names>Martin S.</given-names></name>
<name><surname>Callaghan</surname>
<given-names>Patrick D.</given-names></name>
<name><surname>Smith</surname>
<given-names>Richard F.</given-names></name>
<name><surname>Bates</surname>
<given-names>Alvin C.</given-names></name>
<name><surname>Davidson</surname>
<given-names>James R.</given-names></name>
<name><surname>Battisti</surname>
<given-names>Angello J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2577</fpage>
<lpage>2580</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aurofusarin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002580</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>J. S.</given-names></name>
<name><surname>Martin</surname>
<given-names>G. C. J.</given-names></name>
<name><surname>Rigby</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2580</fpage>
<lpage>2587</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002580">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002580">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 rearrangement of hydrazidic azides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002587</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hegarty</surname>
<given-names>A. F.</given-names></name>
<name><surname>Aylward</surname>
<given-names>J. B.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2587</fpage>
<lpage>2593</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002587">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002587">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 constituents of native Umbelliferae. Part I. Coumarins from dill (&lt;i&gt;Anetheum graveolens&lt;/i&gt; L.)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Page</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2593</fpage>
<lpage>2596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Ottonia vahlii&lt;/i&gt;, Kth. Part I. The volatile constituent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002597</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pinder</surname>
<given-names>A. R.</given-names></name>
<name><surname>Price</surname>
<given-names>S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2597</fpage>
<lpage>2598</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002597">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002597">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-(3-aminopropyl)indoles and 3-indol-1-ylpropionic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002599</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Basanagoudar</surname>
<given-names>L. D.</given-names></name>
<name><surname>Siddappa</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2599</fpage>
<lpage>2601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002599">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002599">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 mass spectrometry. Part XXI. Migrations to carbonium ion centres generated upon electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002601</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Ronayne</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2601</fpage>
<lpage>2607</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002601">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002601">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 high-boiling petroleum distillates. Part XII. Isolation and synthesis of some methylanthracenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002607</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
<name><surname>Stewart</surname>
<given-names>H. N. M.</given-names></name>
<name><surname>Hansell</surname>
<given-names>P. G.</given-names></name>
<name><surname>Kelly</surname>
<given-names>(Miss) K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2607</fpage>
<lpage>2613</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002607">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002607">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pyrido[4,3-&lt;i&gt;d&lt;/i&gt;]pyrimidin-4(3&lt;i&gt;H&lt;/i&gt;)-ones from 4-amino-nicotinic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002613</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ismail</surname>
<given-names>A. G.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2613</fpage>
<lpage>2617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002613">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002613">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and pesticidal activities of derivatives of dinitrophenols. Part VII. Formation of 3,3′,5,5′-tetra-t-butyl-4,4′-diphenoquinone from potassium 2,6-di-t-butyl-4-nitrophenoxide and chloroformates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002618</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pianka</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2618</fpage>
<lpage>2619</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002618">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002618">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 acetylation of phenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002619</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Girdler</surname>
<given-names>R. B.</given-names></name>
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Thadani</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2619</fpage>
<lpage>2624</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002619">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002619">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 decomposition of n-alkyltriarylphosphonium alkoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002625</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hamid</surname>
<given-names>A. Majid</given-names></name>
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2625</fpage>
<lpage>2625</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002625">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002625">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXIX. The synthesis of some fluoroaromatic acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002626</article-id><contrib-group><contrib contrib-type="author">
<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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2626</fpage>
<lpage>2628</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002626">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002626">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. The structure of an unusual product from the reduction of 1-acetylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002628</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
<name><surname>Rea</surname>
<given-names>E. J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2628</fpage>
<lpage>2631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002628">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002628">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The use of t-butyl 2,4,5-trichlorophenyl carbonate in the synthesis of &lt;i&gt;N&lt;/i&gt;-t-butoxycarbonyl amino-acids and their 2,4,5-trichlorophenyl esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002632</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Broadbent</surname>
<given-names>Wallace</given-names></name>
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
<name><surname>Stone</surname>
<given-names>B. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2632</fpage>
<lpage>2636</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002632">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002632">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sulphur monochloride on 2-acyl-1,1-dimethylhydrazines; the formation of tetrazans and oxadiazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002636</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hope</surname>
<given-names>P.</given-names></name>
<name><surname>Wiles</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2636</fpage>
<lpage>2638</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002636">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002636">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 with a known repeating sequence of amino-acids. Synthesis of poly-(α- and γ-L-glutamyl-L-alanylglycine)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>Brian J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2638</fpage>
<lpage>2642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvent effects in nuclear magnetic resonance spectroscopy. Part XIII. Solvent shifts induced by benzene in some α,β-unsaturated compounds. An aid to the determination of stereochemistry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ronayne</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2642</fpage>
<lpage>2645</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some &lt;i&gt;N&lt;/i&gt;-substituted 4-piperidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002645</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baty</surname>
<given-names>J. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>Gurnos</given-names></name>
<name><surname>Moore</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2645</fpage>
<lpage>2647</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002645">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002645">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Indol-3-ylpropane-1,2-dione and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002647</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Hall</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2647</fpage>
<lpage>2650</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002647">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002647">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 abnormal reaction between methyl 1-phenylpyrazole-4-carboxylate and phenylmagnesium bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002650</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
<name><surname>Rackham</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2650</fpage>
<lpage>2651</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002650">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002650">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 oxidative dimerisation of 1,2,3,4-tetrahydro-6-hydroxy-7-isopropylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Falshaw</surname>
<given-names>C. P.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>King</surname>
<given-names>T. J.</given-names></name>
<name><surname>Rodrigo</surname>
<given-names>Seetha I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2652</fpage>
<lpage>2655</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 acridine with maleic and fumaric acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002655</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hurd</surname>
<given-names>Charles D.</given-names></name>
<name><surname>Kotani</surname>
<given-names>Ryotaro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2655</fpage>
<lpage>2656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002655">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002655">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Butadiene sulphone chemistry. Part IV. Evidence for the structures of some butadiene sulphone derivatives from proton magnetic resonance measurements</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002656</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2656</fpage>
<lpage>2657</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002656">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002656">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The acid-catalysed conversion of [1,2,3]triazolo[5,1-&lt;i&gt;c&lt;/i&gt;][1,2,4]benzotriazine derivatives into 1,2,4-benzotriazines and their 1-&lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002658</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tennant</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2658</fpage>
<lpage>2662</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002658">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002658">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The preparation and reactions of trialkyl-lead alkoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002663</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Puddephatt</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2663</fpage>
<lpage>2669</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002663">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002663">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 analogues of angiotensin modified in the 1- or the 4-position</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002669</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cresswell</surname>
<given-names>M. A.</given-names></name>
<name><surname>Hanson</surname>
<given-names>R. W.</given-names></name>
<name><surname>Law</surname>
<given-names>H. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2669</fpage>
<lpage>2675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002669">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002669">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2,4-diethoxycarbonyl-5-hydroxy-5-methyl-3-phenylcyclohexanone with 2,4-dinitrophenylhydrazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002676</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Binns</surname>
<given-names>T. D.</given-names></name>
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2676</fpage>
<lpage>2677</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002676">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002676">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dienone–phenol type rearrangements. Part II. Synthesis of a bicyclic phenol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002677</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>B. R.</given-names></name>
<name><surname>Forrest</surname>
<given-names>L. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2677</fpage>
<lpage>2678</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002677">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002677">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nitro-substituted benzoyl peroxides with pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002679</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Liang</surname>
<given-names>Katherine S. Y.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2679</fpage>
<lpage>2680</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002679">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002679">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 compounds. Part V. Cationic reactions of vinyl acetate with &lt;i&gt;OO&lt;/i&gt;-dialkyl phosphorodithioates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002680</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishiwaki</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2680</fpage>
<lpage>2681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002680">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002680">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 D-psicose derivatives using recent oxidative procedures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002681</article-id><contrib-group><contrib contrib-type="author">
<name><surname>James</surname>
<given-names>K.</given-names></name>
<name><surname>Tatchell</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ray</surname>
<given-names>P. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2681</fpage>
<lpage>2686</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002681">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002681">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination–addition. Part XIV. Addition of carboxylate ions to allenes and acetylenes and use of the adducts in acylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002686</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Appleyard</surname>
<given-names>G. D.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2686</fpage>
<lpage>2691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002686">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002686">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 addition of polyhalogenomethanes and related compounds to norbornadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002691</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Parfitt</surname>
<given-names>L. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2691</fpage>
<lpage>2696</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002691">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002691">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phenylglyoxal hydrate and some aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002696</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
<name><surname>Rehman</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2696</fpage>
<lpage>2698</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002696">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002696">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 gongrine and some other amidinoureido-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002698</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Frankel</surname>
<given-names>Max</given-names></name>
<name><surname>Sheradsky</surname>
<given-names>Tuvia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2698</fpage>
<lpage>2699</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002698">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002698">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Alkoxy-5-amino- and -5-arenesulphonamido-1,3,4-thiadiazoles and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002700</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clarkson</surname>
<given-names>R.</given-names></name>
<name><surname>Landquist</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2700</fpage>
<lpage>2704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002700">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002700">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Index of authors, 1967</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002705</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2705</fpage>
<lpage>2728</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002705">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002705">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Index of subjects, 1967</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39670002729</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>2729</fpage>
<lpage>2755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39670002729">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J39670002729">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Errata</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J3967000X001</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>X001</fpage>
<lpage>X003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J3967000X001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J3/J3967000X001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
</articles>
