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<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J396800FP001</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J396800FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J396800FP001">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/J396800FP003</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J396800FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J396800FP003">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/J396800FP005</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>P005</fpage>
<lpage>P006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J396800FP005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J396800FP005">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The use of thiophen as a chain-extender. Part IV. Synthetic dihydroxyacids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McGhie</surname>
<given-names>J. F.</given-names></name>
<name><surname>Ross</surname>
<given-names>W. A.</given-names></name>
<name><surname>Laney</surname>
<given-names>D. H.</given-names></name>
<name><surname>Barker</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1</fpage>
<lpage>5</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naphthalene chemistry. Part II. Preparation of 1,2,3,4,5,6-hexachloro-7-nitronaphthalene and its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000005</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fenyes</surname>
<given-names>Joseph G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>5</fpage>
<lpage>6</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000005">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Periodate oxidation of 4,4,6,6-tetramethylcyclohexane-1,2,3-triol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McConaghy jun. </surname>
<given-names>John S.</given-names></name>
<name><surname>Bloomfield</surname>
<given-names>Jordan J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>7</fpage>
<lpage>8</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 during dehydrobromination of hydrazidic bromides derived from &lt;i&gt;o&lt;/i&gt;-nitrophenylhydrazine, and a comment on the nitration of &lt;i&gt;p&lt;/i&gt;-dibromobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnish</surname>
<given-names>I. T.</given-names></name>
<name><surname>Gibson</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>8</fpage>
<lpage>11</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphonohydrazides and related compounds. Part VIII. Some aryl carboxylic acid sulphonohydrazides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000011</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>11</fpage>
<lpage>16</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1-&lt;i&gt;O&lt;/i&gt;-octadec-&lt;i&gt;cis&lt;/i&gt;-1′-enyl-L-glycerol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000016</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>16</fpage>
<lpage>21</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000016">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000016">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mycological chemistry. Part XXII. Total synthesis of (±)-aflatoxin-B2</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000022</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>A. H.</given-names></name>
<name><surname>Knight</surname>
<given-names>J. A.</given-names></name>
<name><surname>Roffey</surname>
<given-names>Patrick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>22</fpage>
<lpage>24</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000022">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000022">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The synthesis and reactivity of 2-(&lt;i&gt;NN&lt;/i&gt;-dimethylaminomethyl)ferroceneboronic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000024</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marr</surname>
<given-names>G.</given-names></name>
<name><surname>Moore</surname>
<given-names>R. E.</given-names></name>
<name><surname>Rockett</surname>
<given-names>B. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>24</fpage>
<lpage>27</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000024">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000024">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzocyclo-octatetraenes. Part I. Bromo-derivatives formed in addition reactions of biphenylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000028</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>28</fpage>
<lpage>30</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 ethyl 2-hydroxyindoxyl-2-carboxylate to ethyl 3-hydroxyoxindole-3-carboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Booth</surname>
<given-names>S. R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>30</fpage>
<lpage>32</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 8- and 9-hydroxybenzo[&lt;i&gt;a&lt;/i&gt;]pyrene and the role of the products in benzo[&lt;i&gt;a&lt;/i&gt;]pyrene metabolism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sims</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>32</fpage>
<lpage>34</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bacterial degradation of riboflavin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000034</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Owen</surname>
<given-names>E. C.</given-names></name>
<name><surname>West</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>34</fpage>
<lpage>36</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000034">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000034">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Iron carbonyl complexes from Schiff bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bagga</surname>
<given-names>M. M.</given-names></name>
<name><surname>Flannigan</surname>
<given-names>W. T.</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>
<name><surname>Preston</surname>
<given-names>F. J.</given-names></name>
<name><surname>Reed</surname>
<given-names>R. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>36</fpage>
<lpage>40</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVII. The synthesis of some derivatives and analogues of &lt;i&gt;N&lt;/i&gt;-(5-amino-1-β-D-ribofuranosylimidazole-4-carbonyl)-L-aspartic acid 5′-phosphate (SAICAR) including a competitive enzyme (adenylosuccinate AMP-lyase no. 4.3.2.2.) inhibitor-&lt;i&gt;N&lt;/i&gt;-(5-amino-1-β-D-ribofuranosylimidazole-4-carbonyl)-L-threo-β-methyl aspartic acid 5′-phosphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000040</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>
<name><surname>Wilson</surname>
<given-names>D. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>40</fpage>
<lpage>45</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LIX. Thieno[3′,2′:5,6]thiopyrano[4,3-&lt;i&gt;b&lt;/i&gt;]indoles and thieno[3′,4′:5,6]thiopyrano[4,3-&lt;i&gt;b&lt;/i&gt;]indoles, two new families of &lt;i&gt;pseudo&lt;/i&gt;-azulenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
<name><surname>Croisy</surname>
<given-names>A.</given-names></name>
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>45</fpage>
<lpage>47</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. The tanshinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000048</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baillie</surname>
<given-names>A. C.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>48</fpage>
<lpage>52</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVII. Further studies on esters of 1-hydroxypiperidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. H.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>53</fpage>
<lpage>61</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemotherapy of schistosomiasis. Part IX. &lt;i&gt;p&lt;/i&gt;-Dialkylaminoacylamidophenyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000061</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>R. F.</given-names></name>
<name><surname>Davis</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>61</fpage>
<lpage>63</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000061">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000061">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XXXIV. Nucleophilic addition reactions of pteridine-2-thiol and 2-(methylthio)pteridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000063</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>McCormack</surname>
<given-names>John J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>63</fpage>
<lpage>68</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000063">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000063">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 behaviour of bridged compounds. Part II. Photolytic and some ground state reactions of carbonyl-bridged anhydrides and their decarbonylation products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fuchs</surname>
<given-names>Benzion</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>68</fpage>
<lpage>71</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Fluoropyridine &lt;i&gt;N&lt;/i&gt;-oxide and its reactions with amino-acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000072</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sarantakis</surname>
<given-names>D.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>J. K.</given-names></name>
<name><surname>Tortorella</surname>
<given-names>(Mrs.) C.</given-names></name>
<name><surname>Tortorella</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>72</fpage>
<lpage>73</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000072">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000072">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 some lignans of the 1-phenyl-1,2,3,4-tetrahydronaphthalene series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000074</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>74</fpage>
<lpage>79</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the reaction of benzoyl peroxide with &lt;i&gt;NN&lt;/i&gt;-dialkyl aromatic amines and other related compounds. Part II. Reactions of some primary and secondary amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000080</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roy</surname>
<given-names>R. B.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>80</fpage>
<lpage>83</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000080">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000080">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the reaction of benzoyl peroxide with &lt;i&gt;NN&lt;/i&gt;-dialkyl aromatic amines and other related compounds. Part III. Reactions of some phenolic ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000083</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roy</surname>
<given-names>R. B.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>83</fpage>
<lpage>85</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 XV. Some metabolites of &lt;i&gt;Penicillium citrinum&lt;/i&gt; related to citrinin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000085</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Curtis</surname>
<given-names>R. F.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Nazar</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>85</fpage>
<lpage>93</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000085">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000085">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mass spectra and molecular structure. Part I. Correlation studies and metastable transitions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000093</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hill</surname>
<given-names>(late) H. C.</given-names></name>
<name><surname>Reed</surname>
<given-names>R. I.</given-names></name>
<name><surname>Robert-Lopes</surname>
<given-names>(Miss) M. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>93</fpage>
<lpage>101</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000093">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000093">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydroxyrotenoids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000102</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ringshaw</surname>
<given-names>D. J.</given-names></name>
<name><surname>Smith</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>102</fpage>
<lpage>108</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000102">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000102">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 nezukone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000109</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Keeton</surname>
<given-names>Roger</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>109</fpage>
<lpage>109</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000109">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000109">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenylpropiolic acids. Part VIII. The self-condensation of 3-halogeno-4-methoxyphenylpropiolic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000110</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Moussa</surname>
<given-names>G. E. M.</given-names></name>
<name><surname>Omar</surname>
<given-names>M. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>110</fpage>
<lpage>112</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000110">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000110">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenolic cyclisation. Part I. Novel synthesis of 1-substituted isoquinoline and spiro[cycloalkane-1,1′-isoquinoline] derivatives and its application to the total synthesis of isoquinoline alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000112</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Agui</surname>
<given-names>H.</given-names></name>
<name><surname>Yagi</surname>
<given-names>H.</given-names></name>
<name><surname>Kigasawa</surname>
<given-names>K.</given-names></name>
<name><surname>Sugahara</surname>
<given-names>H.</given-names></name>
<name><surname>Hiiragi</surname>
<given-names>M.</given-names></name>
<name><surname>Hayasaka</surname>
<given-names>T.</given-names></name>
<name><surname>Ishimaru</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>112</fpage>
<lpage>118</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 simple aromatic nitro-compounds with transition-metal oxalates: the question of nitrene intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000119</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Davis</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>119</fpage>
<lpage>126</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000119">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000119">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Aminopivalic acid from hydroxypivalic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000126</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>126</fpage>
<lpage>130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000126">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000126">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;sup&gt;14&lt;/sup&gt;C, &lt;sup&gt;18&lt;/sup&gt;O, and mass spectral study of the pyrolytic formation of carbon suboxide from diacetyltartaric anhydride and acetoxymaleic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000130</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Gilbert</surname>
<given-names>P. A.</given-names></name>
<name><surname>Houghton</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>130</fpage>
<lpage>137</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000130">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000130">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 radiochemical study of the pyrolytic formation of carbon suboxide in the diethyl oxaloacetate–acetic anhydride system: isotopic exchange between the products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000137</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Gilbert</surname>
<given-names>P. A.</given-names></name>
<name><surname>Houghton</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>137</fpage>
<lpage>141</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000137">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000137">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 amidines. Part XXI. [&lt;sup&gt;14&lt;/sup&gt;C]Tricycloquinazoline and hydroxytricycloquinazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>H. G.</given-names></name>
<name><surname>Grout</surname>
<given-names>R. J.</given-names></name>
<name><surname>Partridge</surname>
<given-names>M. W.</given-names></name>
<name><surname>Vipond</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>142</fpage>
<lpage>144</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Halogenation of porphin and octaethylporphin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000145</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Samuels</surname>
<given-names>E.</given-names></name>
<name><surname>Shuttleworth</surname>
<given-names>R.</given-names></name>
<name><surname>Stevens</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>145</fpage>
<lpage>147</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000145">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000145">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sesquiterpenoids. Part XIV. The constitution and stereochemistry of culmorin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000148</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Werstiuk</surname>
<given-names>N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>148</fpage>
<lpage>155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000148">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000148">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The photolytic reactions of α-halogeno-ketones in solutions of olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000155</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Thomson</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>155</fpage>
<lpage>166</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000155">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000155">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 precursors of 1,3,8-naphthalenetriol and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000166</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>166</fpage>
<lpage>169</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000166">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000166">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 heterocyclic compounds. Part III. Studies on &lt;i&gt;Xanthorrhoea&lt;/i&gt; resins. Part IV. Some simple benzindazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000169</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duewell</surname>
<given-names>H.</given-names></name>
<name><surname>Haig</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>169</fpage>
<lpage>172</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000169">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000169">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 pantherine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000172</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Crank</surname>
<given-names>G.</given-names></name>
<name><surname>Ross</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>172</fpage>
<lpage>185</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000172">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000172">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The allylic halogenation of methyl 3-methylbut-2-enoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000185</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahmad</surname>
<given-names>Ilyas</given-names></name>
<name><surname>Gedye</surname>
<given-names>R. N.</given-names></name>
<name><surname>Nechvatal</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>185</fpage>
<lpage>187</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000185">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000185">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Macrocyclic compounds. Part XIII. Isomerisation of macrocyclic alkadienes by potassium dispersed on alumina</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000188</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
<name><surname>Dale</surname>
<given-names>Johannes</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>188</fpage>
<lpage>191</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000188">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000188">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Racemisation. Part I. Racemisation of protoberberines under the conditions of catalytic hydrogenation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000191</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>191</fpage>
<lpage>193</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000191">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000191">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 methanesulphonate of 2,2-dimethylcholesterol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000193</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pathak</surname>
<given-names>S. R.</given-names></name>
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>193</fpage>
<lpage>196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000193">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000193">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-dihydro-1&lt;i&gt;H&lt;/i&gt;-[1]benzothieno[2,3-&lt;i&gt;c&lt;/i&gt;]pyrroles and related aminomethylbenzo[&lt;i&gt;b&lt;/i&gt;]thiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000197</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>Ewing</surname>
<given-names>D. F.</given-names></name>
<name><surname>Saraf</surname>
<given-names>S. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>197</fpage>
<lpage>199</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000197">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000197">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 reaction of nitrosobenzenes with aralkyl amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000199</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Suzuki</surname>
<given-names>Kazuo</given-names></name>
<name><surname>Weisburger</surname>
<given-names>Elizabeth K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>199</fpage>
<lpage>202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000199">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000199">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIII. The mass spectra of dimethyl esters: methoxy-migrations in the mass spectra of dimethyl esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howe</surname>
<given-names>Ian</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>202</fpage>
<lpage>209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. Studies related to the formation and oxidation of reticuline in morphine biosynthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000210</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Foulkes</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hirst</surname>
<given-names>M.</given-names></name>
<name><surname>Parry</surname>
<given-names>G. V.</given-names></name>
<name><surname>Staunton</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>210</fpage>
<lpage>216</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000210">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000210">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The intramolecular acylation of some hex-, hept-, and oct-enoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000217</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Emmett</surname>
<given-names>J. C.</given-names></name>
<name><surname>Coombs</surname>
<given-names>R. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>217</fpage>
<lpage>225</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000217">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000217">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isomerisation of the ethylidene group in the acid moiety of retrorsine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000225</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>225</fpage>
<lpage>226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl azide on cyclic azomethines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ritchie</surname>
<given-names>A. C.</given-names></name>
<name><surname>Rosenberger</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>227</fpage>
<lpage>228</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 prototropic isomerisations. Part I. Preparation of &lt;i&gt;NN&lt;/i&gt;-dialkylprop-1-ynylamines and allenamines from &lt;i&gt;NN&lt;/i&gt;-dialkylprop-2-ynylamines (a novel method for the preparation of ynamines)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000228</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
<name><surname>Viehe</surname>
<given-names>H. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>228</fpage>
<lpage>230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000228">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000228">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitro-steroids. Part V. Spectra of nitro-steroids and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000231</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baylis</surname>
<given-names>A. J.</given-names></name>
<name><surname>Bull</surname>
<given-names>J. R.</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>231</fpage>
<lpage>235</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000231">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000231">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anacrotine, from &lt;i&gt;Crotalaria incana&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000235</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>235</fpage>
<lpage>237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive acyl dipeptides as potential penicillin analogues. Part I. α-(Acylaminosuccinimido)-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000237</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mardle</surname>
<given-names>M. J.</given-names></name>
<name><surname>Nayler</surname>
<given-names>J. H. C.</given-names></name>
<name><surname>Rustidge</surname>
<given-names>D. W.</given-names></name>
<name><surname>Waddington</surname>
<given-names>H. R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>237</fpage>
<lpage>242</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000237">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000237">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactive acyl dipeptides as potential penicillin analogues. Part II. &lt;i&gt;N&lt;/i&gt;-(Acylglycyl)-5-oxo-pyrrolidine-2-carboxylic acids and &lt;i&gt;N&lt;/i&gt;-(acylglycyl)-5,5-dimethyl-2-oxothiazolidine-4-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000242</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>D. B.</given-names></name>
<name><surname>Nayler</surname>
<given-names>J. H. C.</given-names></name>
<name><surname>Waddington</surname>
<given-names>H. R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>242</fpage>
<lpage>245</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000242">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000242">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXII. The chlorination of 5α-cholestan-1-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000245</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>245</fpage>
<lpage>249</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The preparation of some acylated dimethoxyphenylacetic acids and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000250</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
<name><surname>Templeton</surname>
<given-names>Richard</given-names></name>
<name><surname>Munro</surname>
<given-names>H. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>250</fpage>
<lpage>255</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000250">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000250">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 ethyl 2-(2-oxo-3-indolinylidene)-2-hydroxyacetate with propionic anhydride and pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000255</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alam</surname>
<given-names>M.</given-names></name>
<name><surname>Ballantine</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>255</fpage>
<lpage>257</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000255">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000255">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The absolute configurations of some aryl- and alkyl-substituted 3-phenylpropanoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000258</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Watson</surname>
<given-names>M. B.</given-names></name>
<name><surname>Youngson</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>258</fpage>
<lpage>262</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000258">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000258">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 compounds X and Y, two labdane diterpenoids, from &lt;i&gt;Leonotis leonurus&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kaplan</surname>
<given-names>E. R.</given-names></name>
<name><surname>Rivett</surname>
<given-names>D. E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>262</fpage>
<lpage>266</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fluoro-olefins. Part VI. A convenient synthesis of trifluoroacryloyl fluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000266</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Birchall</surname>
<given-names>J. M.</given-names></name>
<name><surname>Clarke</surname>
<given-names>T.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>M. J.</given-names></name>
<name><surname>Iserson</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>266</fpage>
<lpage>268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000266">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000266">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and some reactions of (±)-aleuritic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000268</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>
<name><surname>Jevans</surname>
<given-names>A. W.</given-names></name>
<name><surname>McGhie</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>268</fpage>
<lpage>270</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 homoproaporphine-type compounds by phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000271</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>
<name><surname>Satoh</surname>
<given-names>F.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>271</fpage>
<lpage>275</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000271">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000271">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The permanganate oxidation of thymidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howgate</surname>
<given-names>P.</given-names></name>
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Tittensor</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>275</fpage>
<lpage>279</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 maleic anhydride with dimedone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000279</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Molton</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>279</fpage>
<lpage>280</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000279">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000279">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. The synthesis of allenic cyanohydrins, amino-nitriles, and amino-acids from allenic aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000281</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>281</fpage>
<lpage>283</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000281">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000281">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVIII. The synthesis of allenic amino-acids from allenic bromides and diethyl formylaminomalonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000283</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>283</fpage>
<lpage>287</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000283">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000283">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIX. Synthesis of (±)-hypoglycin A and configuration of the natural isomer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000288</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>288</fpage>
<lpage>290</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000288">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000288">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XX. The preparation of 3-alkyl- and 3,3-dialkylallenenitriles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000291</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greaves</surname>
<given-names>P. M.</given-names></name>
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
<name><surname>Laws</surname>
<given-names>D. R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>291</fpage>
<lpage>294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000291">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000291">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Porphyrin synthesis through &lt;i&gt;b&lt;/i&gt;-oxobilanes and oxophlorins (oxyporphyrins)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000294</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>McGillivray</surname>
<given-names>G.</given-names></name>
<name><surname>Smith</surname>
<given-names>K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>294</fpage>
<lpage>302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000294">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000294">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. The structure and transformations of oxophlorins (oxyporphyrins)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Smith</surname>
<given-names>K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>302</fpage>
<lpage>310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of the constituents of &lt;i&gt;Xylopia aethiopica&lt;/i&gt;. The structure of xylopic acid, a new diterpene acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ekong</surname>
<given-names>D. E. U.</given-names></name>
<name><surname>Ogan</surname>
<given-names>A. U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>311</fpage>
<lpage>312</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Hydrates of ethyl pteridine-4-carboxylate and some methyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000313</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>313</fpage>
<lpage>317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. The preparation and reactions of some alkynyl-lead compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000317</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>317</fpage>
<lpage>322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXII. Some reactions of 2,4-dinitrobenzenesulphenyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000322</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Nakano</surname>
<given-names>T.</given-names></name>
<name><surname>Sammes</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>322</fpage>
<lpage>327</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000322">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000322">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVIII. Preparation and reactions of some 1-substituted biphenylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000328</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Chadwick</surname>
<given-names>J. B.</given-names></name>
<name><surname>Harrison</surname>
<given-names>Charles R.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>328</fpage>
<lpage>330</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000328">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000328">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The photocyclodehydrogenation of some styrylquinolines and styrylisoquinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000330</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>330</fpage>
<lpage>333</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000330">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000330">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. General Lewis acid catalysis of glycoside anomerisation and &lt;i&gt;O&lt;/i&gt;→&lt;i&gt;N&lt;/i&gt;-glycosyl rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000333</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thacker</surname>
<given-names>David</given-names></name>
<name><surname>Ulbricht</surname>
<given-names>T. L. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>333</fpage>
<lpage>337</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000333">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000333">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 3-acetoxy-4-methoxycholesta-3,5-diene with sodium borohydride: effect of methoxyl substitution on the mode of protonation of a conjugated dienolate anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000338</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
<name><surname>Wickramasinghe</surname>
<given-names>J. A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>338</fpage>
<lpage>340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000338">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000338">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homolytic reactions of perfluoroaromatic compounds. Part I. Arylation of hexafluorobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000341</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Claret</surname>
<given-names>P. A.</given-names></name>
<name><surname>Williams</surname>
<given-names>Gareth H.</given-names></name>
<name><surname>Coulson</surname>
<given-names>Judith</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>341</fpage>
<lpage>344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000341">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000341">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2,3,4,6-Penta-azaindenes (‘8-azapurines’). Part III. A new route to the 7-methyl-8-azapurines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Tratt</surname>
<given-names>Kenneth</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>344</fpage>
<lpage>347</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Heterolytic and homolytic decomposition of 1,3-di-&lt;i&gt;o&lt;/i&gt;-cyanophenyltriazene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000348</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>348</fpage>
<lpage>351</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000348">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000348">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIX. Cyclazines and quinolizines from stilbazole with dimethyl acetylenedicarboxylate, and their nuclear magnetic resonance spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Feinberg</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>351</fpage>
<lpage>362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXX. Acetylenedicarboxylic esters with benzopyridines possessing activated methyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000362</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Gagan</surname>
<given-names>J. M. F.</given-names></name>
<name><surname>Harrison</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>362</fpage>
<lpage>378</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000362">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000362">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXL. Methylquinoxalines with acetylenic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000378</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>378</fpage>
<lpage>382</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000378">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000378">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXII. The mass spectra of some azepines obtained from dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000383</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Harrison</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>383</fpage>
<lpage>387</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000383">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000383">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXIII. New adducts from some pyridines and dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000387</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>Hands</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>387</fpage>
<lpage>389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000387">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000387">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXIV. Dimethyl acetylenedicarboxylate with indazole, the triazoles, and diazoaminobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000389</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>389</fpage>
<lpage>391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000389">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000389">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 lactones and mercaptans. Part III. Lactam of 2-(β-carboxyethyl)-2-methylthiazolidine-4-carboxylic acid from α-angelica lactone (pent-3-en-4-olide) and cysteine, and its n.m.r. spectrum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hellström</surname>
<given-names>Nils</given-names></name>
<name><surname>Almqvist</surname>
<given-names>Sven-Olof</given-names></name>
<name><surname>Aamisepp</surname>
<given-names>Margarethe</given-names></name>
<name><surname>Rodmar</surname>
<given-names>Sören</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>392</fpage>
<lpage>398</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000392">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. The preparation and rearrangement of polyfluorovinylamines and of trifluoromethyl trifluorovinyl ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000398</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>398</fpage>
<lpage>405</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000398">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000398">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Schiff bases. Part I. Thermal decarboxylation of α-amino-acids in the presence of ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000406</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Sayyab</surname>
<given-names>A. F.</given-names></name>
<name><surname>Lawson</surname>
<given-names>Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>406</fpage>
<lpage>410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000406">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000406">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Schiff bases. Part II. Some ketimines prepared by decarboxylation of α-amino-acids in the presence of ketones and their reaction and that of aldimines with phenyl isocyanate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Sayyab</surname>
<given-names>A. F.</given-names></name>
<name><surname>Lawson</surname>
<given-names>A.</given-names></name>
<name><surname>Stevens</surname>
<given-names>J. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>411</fpage>
<lpage>415</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The preparation of 3β,15β,17β-trihydroxyandrost-5-ene and the attempted preparation of 3β,15α,17β-trihydroxyandrost-5-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000416</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>416</fpage>
<lpage>421</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000416">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000416">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The reaction of 3β-hydroxy-5α-cholest-1-ene and 3β-hydroxycholest-4-ene with toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl chloride in pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000421</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laing</surname>
<given-names>S. B.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>421</fpage>
<lpage>427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000421">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000421">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mass spectrometric studies on 2-alkylbenzimidazoles. Some evidence for fragmentation &lt;i&gt;via&lt;/i&gt; quinoxalinium ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000428</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>428</fpage>
<lpage>430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Geometrical isomerism in the &lt;i&gt;S&lt;/i&gt;-alkyl thiohydroximate series: a new oxime fragmentation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>J. H.</given-names></name>
<name><surname>Davis</surname>
<given-names>R. H.</given-names></name>
<name><surname>Kirby</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>431</fpage>
<lpage>435</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVIII. Anchimeric acceleration of the aminolysis of esters. The use of mono-esters of catechol in peptide synthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000436</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. H.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>436</fpage>
<lpage>441</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000436">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000436">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Constitution and biosynthesis of capsaicin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000442</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bennett</surname>
<given-names>D. J.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>442</fpage>
<lpage>446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000442">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000442">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Interaction of benzoin and hydrazine hydrochloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Comrie</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>446</fpage>
<lpage>447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Abnormal products from phenolic oxidation of a dihydroxy-1-benzyl-1,2,3,4-tetrahydroisoquinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000447</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Noguchi</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>447</fpage>
<lpage>451</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000447">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000447">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 pteridines. Part V. The synthesis of riboflavin from pteridine precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rowan</surname>
<given-names>Thomas</given-names></name>
<name><surname>Wood</surname>
<given-names>H. C. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>452</fpage>
<lpage>458</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular bonding and relative stabilities of &lt;i&gt;syn&lt;/i&gt;- and &lt;i&gt;anti&lt;/i&gt;-α-hydroximino-ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000459</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 (Mrs.) </surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>459</fpage>
<lpage>460</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000459">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000459">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. Acid-catalysed rearrangement of cholesta-1,3,5-trien-7-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000461</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connolly</surname>
<given-names>J. P.</given-names></name>
<name><surname>Dorchaí</surname>
<given-names>R. Ó.</given-names></name>
<name><surname>Thomson</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>461</fpage>
<lpage>466</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000461">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000461">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1-phenylpyrazol-4-ylmagnesium bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000466</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooklyn</surname>
<given-names>R. J.</given-names></name>
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>466</fpage>
<lpage>468</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000466">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000466">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cinnolines and indoles from 2,β-dinitrostyrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000468</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>468</fpage>
<lpage>470</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000468">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000468">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The hydroboration-oxidation of abietic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000471</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>B. E.</given-names></name>
<name><surname>Myers</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>471</fpage>
<lpage>480</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000471">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000471">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 elucidation of some derivatives of dimethylallyl-coumarin, chromone, quinoline, and phenol from &lt;i&gt;Fagara&lt;/i&gt; species, and from &lt;i&gt;Cedrelopsis grevei&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000481</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eshiett</surname>
<given-names>I. T.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>481</fpage>
<lpage>484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000481">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000481">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 V. The preparation of some stereoisomeric caranamines and a study of their conformations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000484</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Pratt</surname>
<given-names>A. C.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>484</fpage>
<lpage>489</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000484">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000484">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 VI. Pyrolysis and acid-catalysed rearrangements of (+)-car-3-ene and some derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000489</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Hanna</surname>
<given-names>D. P.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>489</fpage>
<lpage>495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000489">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000489">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 convicine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000496</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bien</surname>
<given-names>Shlomo</given-names></name>
<name><surname>Salemnik</surname>
<given-names>Gad</given-names></name>
<name><surname>Zamir</surname>
<given-names>Lolita</given-names></name>
<name><surname>Rosenblum</surname>
<given-names>Myron</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>496</fpage>
<lpage>499</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000496">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000496">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some cyclohexadienones. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Merchant</surname>
<given-names>J. R.</given-names></name>
<name><surname>Desai</surname>
<given-names>V. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>499</fpage>
<lpage>503</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The tautomerism and bromination of some 1-hydroxyindole-2-carboxylic acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000504</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Brookes</surname>
<given-names>C. J. Q.</given-names></name>
<name><surname>Dearnaley</surname>
<given-names>D. P.</given-names></name>
<name><surname>Quest</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>504</fpage>
<lpage>507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000504">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000504">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>γγ-Disubstituted itaconic acids. Part IV. The Stobbe condensation of 6-benzoyltetralin and 2-benzoylnaphthalene with diethyl succinate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Awad</surname>
<given-names>W. I.</given-names></name>
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Fouli</surname>
<given-names>F. A.</given-names></name>
<name><surname>Omran</surname>
<given-names>S. M. A.</given-names></name>
<name><surname>Selim</surname>
<given-names>M. I. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>507</fpage>
<lpage>511</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Glucuronic esters. Part IV. Synthesis of 1-&lt;i&gt;O&lt;/i&gt;-acyl-D-glucopyranuronic acids &lt;i&gt;via&lt;/i&gt; benzyl 1-&lt;i&gt;O&lt;/i&gt;-acyl-2,3,4-tri-&lt;i&gt;O&lt;/i&gt;-benzyl-D-glucopyranuronates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000511</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Keglević</surname>
<given-names>D.</given-names></name>
<name><surname>Pravdić</surname>
<given-names>N.</given-names></name>
<name><surname>Tomašić</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>511</fpage>
<lpage>514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000511">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000511">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. 5- and 6-Alkyl derivatives with an &lt;i&gt;N&lt;/i&gt;-alkyl-&lt;i&gt;N&lt;/i&gt;-(2-chloroethyl)aminomethyl group in the 3-position</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Clarke</surname>
<given-names>K.</given-names></name>
<name><surname>Gore</surname>
<given-names>B.</given-names></name>
<name><surname>Sawhney</surname>
<given-names>S. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>514</fpage>
<lpage>517</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. 3-(&lt;i&gt;N&lt;/i&gt;-alkyl-&lt;i&gt;N&lt;/i&gt;-2-chloroethylaminomethyl)-5- or 7-halogenobenzo[&lt;i&gt;b&lt;/i&gt;]thiophen hydrochlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000518</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>Sawhney</surname>
<given-names>S. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>518</fpage>
<lpage>522</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000518">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000518">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Variations of the terminal amide position in the &lt;i&gt;C&lt;/i&gt;-terminal tetrapeptide amide sequence of the gastrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000522</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>H.</given-names></name>
<name><surname>Laird</surname>
<given-names>A. H.</given-names></name>
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>522</fpage>
<lpage>531</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000522">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000522">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. Variations of the phenylalanyl position in the &lt;i&gt;C&lt;/i&gt;-terminal tetrapeptide amide sequence of the gastrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000531</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>H.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. S.</given-names></name>
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>531</fpage>
<lpage>540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000531">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000531">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry of hindered benzophenones: synthesis and resolution of 3-carboxymethyl-2,2′,4,4′,6,6′-hexamethyl-3′-nitrobenzophenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Narayanan</surname>
<given-names>K. V.</given-names></name>
<name><surname>Selvarajan</surname>
<given-names>R.</given-names></name>
<name><surname>Swaminathan</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>540</fpage>
<lpage>543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 7-methylpyrano[4,3-&lt;i&gt;b&lt;/i&gt;]pyran-2,5-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000543</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheng</surname>
<given-names>F. C.</given-names></name>
<name><surname>Tan</surname>
<given-names>S. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>543</fpage>
<lpage>547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000543">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000543">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Catalytic hydrogenation of perfluoro-(3,6-dihydro-2-methyl-2&lt;i&gt;H&lt;/i&gt;-1,2-oxazine) and of perfluorocyclopentene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000548</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Barlow</surname>
<given-names>M. G.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Lappin</surname>
<given-names>M.</given-names></name>
<name><surname>Matthews</surname>
<given-names>V.</given-names></name>
<name><surname>Tucker</surname>
<given-names>N. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>548</fpage>
<lpage>550</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000548">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000548">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amidines and guanidines related to congocidin. Part IV. Thiophen, pyridine, and benzene analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000550</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. H.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>550</fpage>
<lpage>554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pyrolysis. Part XXIII. Competitive routes in the pyrolysis of 1-anilino-&lt;i&gt;cis&lt;/i&gt;- and -&lt;i&gt;trans&lt;/i&gt;-2-methylcyclohexane-1-carbonitrile, and 1-benzoyloxy-&lt;i&gt;cis&lt;/i&gt;- and -&lt;i&gt;trans&lt;/i&gt;-2-methylcyclohexane-1-carbonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bain</surname>
<given-names>W. C.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>P. D.</given-names></name>
<name><surname>Wright</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>554</fpage>
<lpage>561</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part II. Reaction of 2,3:6,7-di-&lt;i&gt;O&lt;/i&gt;-isopropylidene-5-&lt;i&gt;O&lt;/i&gt;-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl-D-&lt;i&gt;glycero&lt;/i&gt;-D-&lt;i&gt;gulo&lt;/i&gt;-heptofuranose with sodium methoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000562</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Tucker</surname>
<given-names>L. C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>562</fpage>
<lpage>567</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000562">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000562">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part III. Displacements with 1,2:5,6-di-&lt;i&gt;O&lt;/i&gt;-isopropylidene-3-&lt;i&gt;O&lt;/i&gt;-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl-α-D-gulofuranose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000567</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Gent</surname>
<given-names>(Miss) P. A.</given-names></name>
<name><surname>Stacey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>567</fpage>
<lpage>569</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000567">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000567">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Sesquiterpene lactones from the root of &lt;i&gt;Lindera strychnifolia&lt;/i&gt; Vill</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000569</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
<name><surname>Horibe</surname>
<given-names>I.</given-names></name>
<name><surname>Minato</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>569</fpage>
<lpage>572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000569">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000569">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The mechanism of 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/J39680000572</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>572</fpage>
<lpage>575</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The photo-oxidation of tropolone methyl ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000575</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>575</fpage>
<lpage>580</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000575">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000575">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Some reactions 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/J39680000580</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>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>580</fpage>
<lpage>584</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000580">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000580">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The electrolysis of methyl hydrogen &lt;i&gt;cis&lt;/i&gt;-cyclopropane-1,2-dicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000584</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>
<name><surname>Cox</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>584</fpage>
<lpage>587</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000584">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000584">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nonadrides. Part V. Biosynthesis of glauconic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000588</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bloomer</surname>
<given-names>J. L.</given-names></name>
<name><surname>Moppett</surname>
<given-names>C. E.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>588</fpage>
<lpage>591</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000588">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000588">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 diphenyl-1-phenylvinylphosphine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000591</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>591</fpage>
<lpage>595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000591">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000591">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The synthesis of 8-(5-hexyl-2-furyl)octanoic acid, a fatty acid found in &lt;i&gt;Exocarpus&lt;/i&gt; seed oil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000595</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>595</fpage>
<lpage>596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carrageenans. Part III. Oxidative hydrolysis of methylated &lt;i&gt;κ&lt;/i&gt;-carrageenan and evidence for a masked repeating structure</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000596</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>N. S.</given-names></name>
<name><surname>Dolan</surname>
<given-names>T. C. S.</given-names></name>
<name><surname>Rees</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>596</fpage>
<lpage>601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000596">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000596">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carrageenans. Part IV. Variations in the structure and gel properties of &lt;i&gt;κ&lt;/i&gt;-carrageenan, and the characterisation of sulphate esters by infrared spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000602</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>N. S.</given-names></name>
<name><surname>Dolan</surname>
<given-names>T. C. S.</given-names></name>
<name><surname>Penman</surname>
<given-names>A.</given-names></name>
<name><surname>Rees</surname>
<given-names>D. A.</given-names></name>
<name><surname>Mueller</surname>
<given-names>G. P.</given-names></name>
<name><surname>Stancioff</surname>
<given-names>D. J.</given-names></name>
<name><surname>Stanley</surname>
<given-names>N. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>602</fpage>
<lpage>606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000602">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000602">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 prototropic isomerisations. Part II. The isomerisation of &lt;i&gt;N&lt;/i&gt;-prop-2-ynyl heterocycles into &lt;i&gt;N&lt;/i&gt;-substituted allenes and acetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000606</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
<name><surname>Reimlinger</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>606</fpage>
<lpage>608</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000606">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000606">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LX. New nitrogen heterocycles bearing a selenophen, thiophen, thiazole, or pyrazole ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000609</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Saint-Ruf</surname>
<given-names>G.</given-names></name>
<name><surname>Martani</surname>
<given-names>A.</given-names></name>
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
<name><surname>Balucani</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>609</fpage>
<lpage>611</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000609">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000609">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isothiazoles. Part XI. Carbinols, aryl ketones, and aminomethyl derivatives of isothiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000611</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Layton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Lunt</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>611</fpage>
<lpage>614</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000611">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000611">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Dehydro-&lt;i&gt;O&lt;/i&gt;-(2-pyrrolylcarbonyl)virgiline, an alkaloid from &lt;i&gt;Readea membranaceae&lt;/i&gt; Gillespie (rubiaceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000615</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Manchanda</surname>
<given-names>A. H.</given-names></name>
<name><surname>Nabney</surname>
<given-names>J.</given-names></name>
<name><surname>Young</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>615</fpage>
<lpage>616</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000615">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000615">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 conjugated double bonds. Part II. The occurrence of 1,4- or 1,2-addition in the reduction of some aryl αβ-unsaturated ketones with metal hydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000616</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Iqbal</surname>
<given-names>K.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>616</fpage>
<lpage>620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000616">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000616">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. Total synthesis of (±)-lindestrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Minato</surname>
<given-names>Hitoshi</given-names></name>
<name><surname>Nagasaki</surname>
<given-names>Tohru</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>621</fpage>
<lpage>624</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoro-heterocyclic compounds. Part XI. Factors controlling the orientation of nucleophilic substitution in octafluoro-3,3′-bipyridyl and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000625</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Lomas</surname>
<given-names>D.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>625</fpage>
<lpage>629</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000625">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000625">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 symmetrically trisubstituted benzene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000630</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cochrane</surname>
<given-names>W. P.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Stevens</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>630</fpage>
<lpage>632</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000630">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000630">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation and diazotisation of some &lt;i&gt;o&lt;/i&gt;- and &lt;i&gt;p&lt;/i&gt;-aminophenyl benzoates and benzamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000632</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Vickers</surname>
<given-names>S.</given-names></name>
<name><surname>Triggle</surname>
<given-names>D. J.</given-names></name>
<name><surname>Garrison</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>632</fpage>
<lpage>634</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000632">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000632">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 epoxides. Part XV. Boron trifluoride-catalysed rearrangements of 5,6-epoxides in the 4,4-dimethylcholestane series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000635</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blunt</surname>
<given-names>J. W.</given-names></name>
<name><surname>Hartshorn</surname>
<given-names>M. P.</given-names></name>
<name><surname>Kirk</surname>
<given-names>D. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>635</fpage>
<lpage>640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000635">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000635">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Osmium tetroxide-catalysed oxidation of olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000640</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cairns</surname>
<given-names>J. F.</given-names></name>
<name><surname>Roberts</surname>
<given-names>H. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>640</fpage>
<lpage>642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The dithiole series. Part III. Dithiolocyanines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Easton</surname>
<given-names>D. B. J.</given-names></name>
<name><surname>Leaver</surname>
<given-names>D.</given-names></name>
<name><surname>McKinnon</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>642</fpage>
<lpage>644</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sucrose and tetrahydro-2-hydroxymethylpyran with dichlorosilanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000644</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>S. A.</given-names></name>
<name><surname>Harnden</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>644</fpage>
<lpage>648</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000644">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000644">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 substitutions with rearrangements. Part I. Products of the chlorination of 1-naphthol and some related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000648</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>648</fpage>
<lpage>652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. A transannular hydrogen transfer encountered in the formation of 1α,5-cyclo-5α-cholest-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000653</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laing</surname>
<given-names>S. B.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>653</fpage>
<lpage>656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Addition and metallation in the reaction of n-butyl-lithium with 2-ferrocenylpyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000656</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>D. J.</given-names></name>
<name><surname>Rockett</surname>
<given-names>B. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>656</fpage>
<lpage>659</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000656">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000656">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 sulphides with iodobenzene dichloride in aqueous pyridine. Synthesis of sulphoxides free from sulphone and &lt;sup&gt;18&lt;/sup&gt;O-labelled sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000659</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barbieri</surname>
<given-names>G.</given-names></name>
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>659</fpage>
<lpage>663</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000659">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000659">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryne chemistry. Part V. Some addition reactions of tetrafluorobenzyne</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000664</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brewer</surname>
<given-names>J. P. N.</given-names></name>
<name><surname>Eckhard</surname>
<given-names>I. F.</given-names></name>
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
<name><surname>Marples</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>664</fpage>
<lpage>676</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000664">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000664">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies of tautomeric systems. Part I. Triacylmethanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000676</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>676</fpage>
<lpage>678</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000676">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000676">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 unexpected products from the treatment of organoboranes from α,β-unsaturated ketones with acetic acid–acetic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000679</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>K.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>679</fpage>
<lpage>681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000679">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000679">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of picryl azide with olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000682</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Wedgwood</surname>
<given-names>(Mrs.) J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>682</fpage>
<lpage>684</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000682">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000682">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transesterification versus nucleophilic displacement in cyclic and open-chain organic sulphites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000684</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bristow</surname>
<given-names>P. A.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>684</fpage>
<lpage>687</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000684">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000684">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Nitration and sulphonation of chloro-(5,6,7,8)-4-hydroxy-cinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000687</article-id><contrib-group><contrib contrib-type="author">
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>687</fpage>
<lpage>695</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000687">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000687">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Restricted rotation about the aliphatic carbon–carbon bond in 1,2-disubstituted tetra-arylethanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000696</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burchill</surname>
<given-names>P. J. M.</given-names></name>
<name><surname>Thorne</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>696</fpage>
<lpage>700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000696">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000696">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrogenolysis reactions of some polychlorinated norborn-2-enes, and the synthesis of 1,4-dichloronorborn-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000700</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>700</fpage>
<lpage>704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000700">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000700">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The addition of methanethiol, bromotrichloromethane, and chloroform to 1,4-dichloronorborn-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000705</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>
<name><surname>Rowley</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>705</fpage>
<lpage>708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000705">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000705">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The 2-methylenenorborn-3-yl ↔ norborn-2-en-2-ylmethyl allylic radical system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000709</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>709</fpage>
<lpage>711</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000709">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. &lt;i&gt;para&lt;/i&gt;-Quinols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>B. R.</given-names></name>
<name><surname>Woodgate</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>712</fpage>
<lpage>715</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Variations of the aspartyl position in the &lt;i&gt;C&lt;/i&gt;-terminal tetrapeptide amide sequence of the gastrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000715</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>H.</given-names></name>
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. M.</given-names></name>
<name><surname>Smithers</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>715</fpage>
<lpage>725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000715">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000715">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. Variations of the methionyl position in the &lt;i&gt;C&lt;/i&gt;-terminal tetrapeptide amide sequence of the gastrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>726</fpage>
<lpage>733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000726">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The reduction of pyrimidines with complex metal hydrides to give 1,6-dihydropyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000733</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>733</fpage>
<lpage>740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000733">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of the &lt;i&gt;N&lt;/i&gt;-carbazolyl radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000740</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
<name><surname>White</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>740</fpage>
<lpage>745</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000740">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000740">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments with thioacetals and related substances. Part IV. Anionotropic rearrangements of &lt;i&gt;gem&lt;/i&gt;-bisalkylthio-propenes and -butenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000746</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rothstein</surname>
<given-names>Eugene</given-names></name>
<name><surname>Stanbank</surname>
<given-names>Derek J.</given-names></name>
<name><surname>Whiteley</surname>
<given-names>Ronald</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>746</fpage>
<lpage>752</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000746">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000746">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments with thioacetals and related substances. Part V. Reactions of some chloro-&lt;i&gt;gem&lt;/i&gt;-bisalkylthiobutanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000753</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rothstein</surname>
<given-names>Eugene</given-names></name>
<name><surname>Stanbank</surname>
<given-names>Derek J.</given-names></name>
<name><surname>Whiteley</surname>
<given-names>Ronald</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>753</fpage>
<lpage>760</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000753">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000753">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. Analogues of gastrin containing leucine in place of methionine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000761</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenner</surname>
<given-names>G. W.</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>761</fpage>
<lpage>764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000761">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000761">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 spectra of some benzo[&lt;i&gt;b&lt;/i&gt;]thiophen derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000764</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Ewing</surname>
<given-names>D. F.</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>764</fpage>
<lpage>769</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000764">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000764">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-bromo-2-pyrones and their reactions with bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000769</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>769</fpage>
<lpage>775</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000769">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000769">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 esters of Feist's acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000776</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>776</fpage>
<lpage>778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000776">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000776">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 salts of 2-substituted acrylic acids. Novel reduction of a vinyl bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilchrist</surname>
<given-names>T. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>779</fpage>
<lpage>782</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 in &lt;i&gt;NN&lt;/i&gt;-dimethylformamide. Part II. Halogen replacement in the anthraquinone series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000783</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lord</surname>
<given-names>W. M.</given-names></name>
<name><surname>Peters</surname>
<given-names>A. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>783</fpage>
<lpage>785</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000783">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000783">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIX. The structure of digacetigenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000786</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Hughes</surname>
<given-names>N. W.</given-names></name>
<name><surname>Lack</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>786</fpage>
<lpage>793</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000786">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000786">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 adducts of 9-anthrol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000793</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>793</fpage>
<lpage>795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000793">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000793">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoroalkyl derivatives of nitrogen. Part XXVII. Some reactions of &lt;i&gt;NN&lt;/i&gt;-bistrifluoromethylvinylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000796</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alexander</surname>
<given-names>E. S.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Newlands</surname>
<given-names>M. J.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>796</fpage>
<lpage>801</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000796">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000796">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Action of primary and secondary aromatic amines on cephalosporanic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000801</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradshaw</surname>
<given-names>(Miss) J.</given-names></name>
<name><surname>Eardley</surname>
<given-names>S.</given-names></name>
<name><surname>Long</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>801</fpage>
<lpage>806</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000801">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000801">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the diterpene marrubiin and its congeners</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000807</article-id><contrib-group><contrib contrib-type="author">
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>807</fpage>
<lpage>810</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000807">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000807">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 glutinosin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000810</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grove</surname>
<given-names>John Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>810</fpage>
<lpage>812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000810">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000810">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Highly condensed polycyclic systems. Part I. Tetracyclo-[6,4,0,0&lt;sup&gt;4,12&lt;/sup&gt;,0&lt;sup&gt;5,9&lt;/sup&gt;]dodec-10-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000812</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akhtar</surname>
<given-names>I. A.</given-names></name>
<name><surname>Fray</surname>
<given-names>G. I.</given-names></name>
<name><surname>Yarrow</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>812</fpage>
<lpage>815</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000812">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000812">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structural effects in reactions of organophosphorus compounds. I. Reactions of phosphorus oxychloride with hindered phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000815</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kosolapoff</surname>
<given-names>Gennady M.</given-names></name>
<name><surname>Arpke</surname>
<given-names>Charles K.</given-names></name>
<name><surname>Lamb</surname>
<given-names>Robert W.</given-names></name>
<name><surname>Reich</surname>
<given-names>Hans</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>815</fpage>
<lpage>818</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000815">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000815">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Radical abstraction of iodine from aromatic iodides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000819</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brydon</surname>
<given-names>D. L.</given-names></name>
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>819</fpage>
<lpage>824</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000819">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000819">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. 1,2,4-Triazolyl ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000824</article-id><contrib-group><contrib contrib-type="author">
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>824</fpage>
<lpage>830</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000824">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000824">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photocyclisation of anilino-pyridines to carbolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000831</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>V. M.</given-names></name>
<name><surname>Cox</surname>
<given-names>A.</given-names></name>
<name><surname>Herbert</surname>
<given-names>E. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>831</fpage>
<lpage>833</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000831">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000831">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steroids. Part XII. A 1,10-seco-steroid from the pyrolysis of bisergostatrienol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flanagan</surname>
<given-names>P. J.</given-names></name>
<name><surname>Thomson</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>833</fpage>
<lpage>836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. Nitration of 5-acetamido-2-phenylpyrimidine and the synthesis of some 5-nitropyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caton</surname>
<given-names>M. P. L.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>836</fpage>
<lpage>838</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structural effects in reactions of organophosphorus compounds. II. Reaction of Grignard reagents with phosphonic dichlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000839</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown jun. </surname>
<given-names>Alfred D.</given-names></name>
<name><surname>Kosolapoff</surname>
<given-names>Gennady M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>839</fpage>
<lpage>842</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000839">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000839">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Persulphate oxidation of carboxylic acids. Part III. Oxidation of &lt;i&gt;cis&lt;/i&gt;-cinnamic and biphenyl-2-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000842</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>P. Margaret</given-names></name>
<name><surname>Russell</surname>
<given-names>J.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
<name><surname>Wylie</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>842</fpage>
<lpage>848</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000842">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000842">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 biphenyl-2-carboxylic acid silver salts with iodine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000848</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chalmers</surname>
<given-names>D. J.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>848</fpage>
<lpage>850</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000848">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000848">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Extractives from &lt;i&gt;Tabebuia chrysantha&lt;/i&gt; nichols and other bignoniaceae</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000850</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>850</fpage>
<lpage>853</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000850">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000850">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Anthraquinones and related naphthalenic compounds in &lt;i&gt;Galium&lt;/i&gt; spp. and in &lt;i&gt;Asperula odorata&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000854</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>854</fpage>
<lpage>857</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000854">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000854">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. The quinonoid constituents of &lt;i&gt;Pyrola media&lt;/i&gt; Sw. (Pyrolaceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000857</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>857</fpage>
<lpage>860</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000857">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000857">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XX. Functionally substituted fulvenes and cyclopentadienes as potential precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000860</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>860</fpage>
<lpage>863</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000860">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000860">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Stobbe condensation. Part IV. The cyclisation of 3-methoxycarbonyl-&lt;i&gt;cis&lt;/i&gt;-4-(1- and 2-naphthyl)but-3-enoic acids into the corresponding phenanthrene derivatives, and of 3-methoxycarbonyl-&lt;i&gt;cis&lt;/i&gt;-4-(5,6,7,8-tetrahydro-2-naphthyl)but-3-enoic acid into the corresponding isomeric phenanthrene and anthracene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000863</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abdel-Wahhab</surname>
<given-names>(Mrs.) S. M.</given-names></name>
<name><surname>El-Assal</surname>
<given-names>Lanson S.</given-names></name>
<name><surname>Ramses</surname>
<given-names>(Miss) Nadia</given-names></name>
<name><surname>Shehab</surname>
<given-names>(Mrs.) A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>863</fpage>
<lpage>866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000863">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000863">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Stobbe condensation. Part V. The cyclisation of 3-methoxy-carbonyl-&lt;i&gt;cis&lt;/i&gt;-4-(2-furyl)but-3-enoic acid and αβ-difurfurylidenesuccinic anhydride to the corresponding benzofuran derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000867</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abdel-Wahhab</surname>
<given-names>(Mrs.) S. M.</given-names></name>
<name><surname>El-Assal</surname>
<given-names>Lanson S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>867</fpage>
<lpage>869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000867">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000867">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photoalkylation of &lt;i&gt;γ&lt;/i&gt;-butyrolactone with olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000870</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elad</surname>
<given-names>D.</given-names></name>
<name><surname>Friedman</surname>
<given-names>G.</given-names></name>
<name><surname>Youssefyeh</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>870</fpage>
<lpage>875</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000870">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000870">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 styrene and related compounds with &lt;i&gt;NN&lt;/i&gt;-dichlorosulphonamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000876</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Seden</surname>
<given-names>T. P.</given-names></name>
<name><surname>Turner</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>876</fpage>
<lpage>878</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000876">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000876">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The alkylation of 8-hydroxy-6-methylthiopurine and the reactivity of 8-hydroxy-3-methyl-6-methylthiopurine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000878</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Diller</surname>
<given-names>D.</given-names></name>
<name><surname>Neiman</surname>
<given-names>Z.</given-names></name>
<name><surname>Bergmann</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>878</fpage>
<lpage>881</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000878">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000878">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-, aryl-, and acyl-metal(III) complexes of aetioporphyrin I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000881</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clarke</surname>
<given-names>D. A.</given-names></name>
<name><surname>Dolphin</surname>
<given-names>D.</given-names></name>
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Pinnock</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>881</fpage>
<lpage>885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000881">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000881">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photoaddition of acrylonitrile to benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000886</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Job</surname>
<given-names>B. E.</given-names></name>
<name><surname>Littlehailes</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>886</fpage>
<lpage>889</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000886">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000886">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryne chemistry. Part IX. Cycloaddition reactions of the isomeric trifluorobenzynes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>R.</given-names></name>
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>889</fpage>
<lpage>892</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 polycyclic compounds. Part VIII. Friedel–Crafts acylation with anhydrides of tricarboxylic acids. Synthesis of 16,17-dihydro-17-methyl-15&lt;i&gt;H&lt;/i&gt;-cyclopenta[&lt;i&gt;a&lt;/i&gt;]phenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000893</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tatta</surname>
<given-names>K. R.</given-names></name>
<name><surname>Bardhan</surname>
<given-names>(the late) J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>893</fpage>
<lpage>900</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000893">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000893">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phosphorylated sugars. Part XII. An unexpected phosphate-group migration during the attempted preparation of 2-deoxy-d-&lt;i&gt;erythro&lt;/i&gt;-pentose 5-(dihydrogen phosphate) from glucometasaccharinic acid 6-phosphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000901</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Trigalo</surname>
<given-names>F.</given-names></name>
<name><surname>Szabó</surname>
<given-names>Patricia</given-names></name>
<name><surname>Szabó</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>901</fpage>
<lpage>905</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000901">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000901">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aliphatic hydroxy-acids. Part III. Syntheses with alkyl 2-acetoxy-3-carboxypropionates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000906</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
<name><surname>Latham</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>906</fpage>
<lpage>910</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000906">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000906">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. Variations of the tryptophyl position in the &lt;i&gt;C&lt;/i&gt;-terminal tetrapeptide amide sequence of the gastrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000910</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>H.</given-names></name>
<name><surname>Morley</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>910</fpage>
<lpage>915</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000910">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000910">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 9-[&lt;i&gt;p&lt;/i&gt;-(bis-2-chloroethylamino)phenyl]-6-substituted purines as potential cytotoxic agents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000915</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spaziano</surname>
<given-names>V. T.</given-names></name>
<name><surname>Shah</surname>
<given-names>H. C.</given-names></name>
<name><surname>Chou</surname>
<given-names>T. C.</given-names></name>
<name><surname>Price</surname>
<given-names>C. C.</given-names></name>
<name><surname>Lin</surname>
<given-names>H. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>915</fpage>
<lpage>918</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000915">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000915">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The action of hydroxylamine on 4-hydroxypteridine and its methyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000919</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Neath</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>919</fpage>
<lpage>922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000919">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000919">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unusual reactions of aryl diazonium sulphonates possessing &lt;i&gt;ortho&lt;/i&gt;-t-amino-substituents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000923</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainsworth</surname>
<given-names>D. P.</given-names></name>
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>923</fpage>
<lpage>926</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000923">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000923">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXV. Methyl pyrimidines and methyl pyrazines with dimethyl acetylenedicarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000926</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>Stubbs</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>926</fpage>
<lpage>929</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000926">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000926">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. Investigations on the biosynthesis of sinomenine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000929</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Kirby</surname>
<given-names>(Mrs.) A. J.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>929</fpage>
<lpage>936</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000929">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000929">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Some reactions of 1α,5-cyclo-5α-cholest-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000937</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laing</surname>
<given-names>S. B.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>937</fpage>
<lpage>941</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000937">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000937">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;i&gt;O&lt;/i&gt;-β-D-glucosyl-8-&lt;i&gt;C&lt;/i&gt;-β-D-glucosyl-4′-&lt;i&gt;O&lt;/i&gt;-methylapigenin. A new flavone from &lt;i&gt;Trema aspera&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000941</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oelrichs</surname>
<given-names>P.</given-names></name>
<name><surname>Marshall</surname>
<given-names>J. T. B.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>941</fpage>
<lpage>947</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 routes to pyrazino[2,3-&lt;i&gt;b&lt;/i&gt;]quinoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000947</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nyquist</surname>
<given-names>E. B.</given-names></name>
<name><surname>Joullie</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>947</fpage>
<lpage>949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000947">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000947">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 benzil mono- and bis-arylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000949</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>El-Shafei</surname>
<given-names>Z. M.</given-names></name>
<name><surname>Hashem</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>949</fpage>
<lpage>951</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000949">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000949">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;Croton&lt;/i&gt; species. Part VIII. Morphinandienone derivatives from &lt;i&gt;Croton linearis&lt;/i&gt; Jacq.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000951</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
<name><surname>Husbands</surname>
<given-names>G. E. M.</given-names></name>
<name><surname>Stuart</surname>
<given-names>K. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>951</fpage>
<lpage>957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000951">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000951">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nitration of 1-thiaphenalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000957</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>C. C.</given-names></name>
<name><surname>Sutcliffe</surname>
<given-names>F. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>957</fpage>
<lpage>960</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000957">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000957">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Salts of 4-alkyl-3,5-dicyano-6-mercapto-2-pyridinethiones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000960</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brunskill</surname>
<given-names>J. S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>960</fpage>
<lpage>966</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000960">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000960">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Friedel-Crafts acylation of aromatic halogen derivatives. Part III. The benzoylation of chlorobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000966</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodman</surname>
<given-names>P. A.</given-names></name>
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>966</fpage>
<lpage>969</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000966">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000966">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Some reactions with furans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000969</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baggaley</surname>
<given-names>A. J.</given-names></name>
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>969</fpage>
<lpage>974</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000969">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000969">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 carbonhydrates. Part VIII. Intramolecular allylic isomerisations of 1-deoxyald-1-enopyranose (2-hydroxyglycal) esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000974</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>
<name><surname>Sankey</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>974</fpage>
<lpage>977</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000974">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000974">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cigarette smoke. Part X. Evidence for 1,5-hydrogen transfer in the formation of non-conjugated isoprenoid polyolefins during pyrolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000977</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dare</surname>
<given-names>D. L.</given-names></name>
<name><surname>Entwistle</surname>
<given-names>I. D.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>977</fpage>
<lpage>980</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000977">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000977">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXX. Some properties of the cholest-5-ene-3β,7ξ-diols and their esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000981</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Newman</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>981</fpage>
<lpage>983</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000981">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000981">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Water-soluble polysaccharides of the red alga &lt;i&gt;Laurencia pinnatifida&lt;/i&gt;. Part I. Constituent units</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000983</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowker</surname>
<given-names>D. M.</given-names></name>
<name><surname>Turvey</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>983</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000983">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000983">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Water-soluble polysaccharides of the red alga &lt;i&gt;Laurencia pinnatifida&lt;/i&gt;. Part II. Methylation analysis of the galactan sulphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000989</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowker</surname>
<given-names>D. M.</given-names></name>
<name><surname>Turvey</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>989</fpage>
<lpage>992</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000989">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000989">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 aromatic vinyl sulphonyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000992</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Culbertson</surname>
<given-names>B. M.</given-names></name>
<name><surname>Dietz</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>992</fpage>
<lpage>993</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000992">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000992">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 spectrometry of dimedone and anhydrodimedone derivatives of some aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000993</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blythin</surname>
<given-names>D. J.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>993</fpage>
<lpage>995</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000993">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000993">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in the dithiocarbamate series. Part I. Synthesis and decomposition of some 4-hydroxybenzyl dithiocarbamates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680000996</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fitton</surname>
<given-names>A. O.</given-names></name>
<name><surname>Rigby</surname>
<given-names>A.</given-names></name>
<name><surname>Hurlock</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>996</fpage>
<lpage>999</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680000996">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680000996">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bromination of cumene and some 4-hydroxycumenes with &lt;i&gt;N&lt;/i&gt;-bromosuccinimide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001000</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fitton</surname>
<given-names>A. O.</given-names></name>
<name><surname>Rigby</surname>
<given-names>A.</given-names></name>
<name><surname>Hurlock</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1000</fpage>
<lpage>1001</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001000">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001000">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 substituted benzoic acids. Part III. Isopropylbenzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>Malcolm</given-names></name>
<name><surname>Supanekar</surname>
<given-names>V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1001</fpage>
<lpage>1003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and novel enol-ether addition in homoproaporphines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001003</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Satoh</surname>
<given-names>F.</given-names></name>
<name><surname>Yagi</surname>
<given-names>H.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1003</fpage>
<lpage>1005</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001003">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrenes. Part I. Modified syntheses of β-carboline derivatives through nitrene intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001006</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>
<name><surname>Yamanaka</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1006</fpage>
<lpage>1007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2,3,6-Tri-&lt;i&gt;O&lt;/i&gt;-benzoyl-α-D-glucopyranosyl bromide: syntheses, methanolyses, and attempted self-condensations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wadsworth</surname>
<given-names>William W.</given-names></name>
<name><surname>Schroeder</surname>
<given-names>Leland R.</given-names></name>
<name><surname>Green</surname>
<given-names>John W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1008</fpage>
<lpage>1011</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 amino-acid and peptide derivatives. Part I. Benzyloxycarbonyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Jones</surname>
<given-names>J. H.</given-names></name>
<name><surname>Liberek</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1011</fpage>
<lpage>1016</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIII. Formation and rearrangement of 2-methylisoindoline-1-spirocyclohexa-2′,5′-diene-3,4′-dione. Synthesis of the octahydro-derivative of an unsaturated dimer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001017</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collington</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1017</fpage>
<lpage>1020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001017">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001017">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIV. Catalysed decomposition of diazonium fluoroborates from amino-&lt;i&gt;N&lt;/i&gt;-methyl-naphthanilides and -&lt;i&gt;N&lt;/i&gt;-naphthylbenzamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001021</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collington</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
<name><surname>Wessels)</surname>
<given-names>E. le R. Bradley (née</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1021</fpage>
<lpage>1025</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001021">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001021">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXV. Aromatisation of some spiro-cyclohexadiene dimers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collington</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1026</fpage>
<lpage>1028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrolysis of 3-phenyl-1,2,3-benzotriazin-4-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001028</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1028</fpage>
<lpage>1029</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrolysis of potassium 2′-fluoro- and 2′-bromo-biphenyl-2-carboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collington</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1030</fpage>
<lpage>1031</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 β-amyrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001031</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Lier</surname>
<given-names>E. F.</given-names></name>
<name><surname>McGhie</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1031</fpage>
<lpage>1040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001031">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001031">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LIV. Synthesis of isodiotigenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
<name><surname>Lukacs</surname>
<given-names>Gabor</given-names></name>
<name><surname>Yasuda</surname>
<given-names>Fumio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1041</fpage>
<lpage>1044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The peroxyacid oxidation of acridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Adcock</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1045</fpage>
<lpage>1047</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dipterocarpaceae resins. Part I. Triterpene acids of &lt;i&gt;Dryobalanops aromatica&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheung</surname>
<given-names>H. T.</given-names></name>
<name><surname>Feng</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1047</fpage>
<lpage>1051</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pseudouridine and of 5-β-D-ribofuranosyluridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001051</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Burdon</surname>
<given-names>M. G.</given-names></name>
<name><surname>Slatcher</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1051</fpage>
<lpage>1053</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001051">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001051">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 the gibberellins. Part III</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001054</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>B. E.</given-names></name>
<name><surname>Norton</surname>
<given-names>K.</given-names></name>
<name><surname>Stewart</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1054</fpage>
<lpage>1063</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001054">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001054">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXI. Extractives from &lt;i&gt;Daniellia&lt;/i&gt; species. The structure of a new diterpene, ozic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001063</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>Okogun</surname>
<given-names>J. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1063</fpage>
<lpage>1066</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001063">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001063">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXII. The diterpenes of &lt;i&gt;Oxystigma oxyphyllum&lt;/i&gt; Harms</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001067</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>Okogun</surname>
<given-names>J. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1067</fpage>
<lpage>1070</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001067">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001067">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 2,2-dialkyl-1,2-dihydroquinolines. Part III. Reactions of 4-bromomethyl-1,2-dihydro-2,2-dimethylquinolines with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001071</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1071</fpage>
<lpage>1073</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001071">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001071">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 2,2-dialkyl-1,2-dihydroquinolines. Part IV. 4,5-Dihydro-4,4-dimethyl-1&lt;i&gt;H&lt;/i&gt;-1,2-dithiolo[3,4-&lt;i&gt;c&lt;/i&gt;]quinoline-1-thiones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1074</fpage>
<lpage>1075</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 2,2-dialkyl-1,2-dihydroquinolines. Part V. The dimer of 1,2-dihydro-2,2,4-trimethylquinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001075</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. P.</given-names></name>
<name><surname>Tidd</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1075</fpage>
<lpage>1077</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001075">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001075">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>5-Thiation of 1,2-dithiole-3-thiones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001077</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1077</fpage>
<lpage>1082</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001077">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001077">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinolizinines. Part XI. Synthesis of some amino-quinolizinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001082</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1082</fpage>
<lpage>1087</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001082">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001082">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Reactions of some 1- and 2-aminoquinolizinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001088</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1088</fpage>
<lpage>1090</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Branched-chain sugars. Part VIII. A contribution to the chemistry of 2-&lt;i&gt;C&lt;/i&gt;-methyl-L-arabinose and -ribose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001091</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferrier</surname>
<given-names>R. J.</given-names></name>
<name><surname>Overend</surname>
<given-names>W. G.</given-names></name>
<name><surname>Rafferty</surname>
<given-names>G. A.</given-names></name>
<name><surname>Wall</surname>
<given-names>H. M.</given-names></name>
<name><surname>Williams</surname>
<given-names>N. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1091</fpage>
<lpage>1095</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fluorinated acetylenes. Part I. The preparation of &lt;i&gt;NN&lt;/i&gt;-bistrifluoromethylethynylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Freear</surname>
<given-names>J.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1096</fpage>
<lpage>1103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXVIII. The reaction of hydrazines with 6-chloro-2-chloromethyl-4-phenylquinazoline 3-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001103</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Derieg</surname>
<given-names>M. E.</given-names></name>
<name><surname>Fryer</surname>
<given-names>R. Ian</given-names></name>
<name><surname>Sternbach</surname>
<given-names>L. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1103</fpage>
<lpage>1105</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001103">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001103">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation and conformation of 1-alkyl- and 1-aryl-4-t-butylcyclohexanols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001106</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Percy</surname>
<given-names>R. K.</given-names></name>
<name><surname>Richards</surname>
<given-names>(Mrs.) E. E.</given-names></name>
<name><surname>Young</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1106</fpage>
<lpage>1109</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001106">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001106">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bicyclononanes. Part III. Chair–boat equilibria in bicyclo[3,3,1]nonanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001110</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Appleton</surname>
<given-names>R. A.</given-names></name>
<name><surname>Egan D.H.G. </surname>
<given-names>Sister C.</given-names></name>
<name><surname>Evans</surname>
<given-names>J. M.</given-names></name>
<name><surname>Graham</surname>
<given-names>S. H.</given-names></name>
<name><surname>Dixon</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1110</fpage>
<lpage>1115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001110">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001110">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 1-1′-naphthyl-8-phenylnaphthalene (8-phenyl-1,1′-binaphthyl)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Shuttleworth</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1115</fpage>
<lpage>1120</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphonation of arylpyrazoles. Part II. Some 1-phenylpyrazolesulphonic acids and their derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001120</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barry</surname>
<given-names>W. J.</given-names></name>
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
<name><surname>Khatkhate</surname>
<given-names>G. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1120</fpage>
<lpage>1122</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001120">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001120">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Desulphuration of heterocyclic thiols with nickel boride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Grantham</surname>
<given-names>R. K.</given-names></name>
<name><surname>Lydiate</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1122</fpage>
<lpage>1124</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Some 2-substituted derivatives of ethyl pteridine-4-carboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001124</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Jim</given-names></name>
<name><surname>Pendergast</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1124</fpage>
<lpage>1127</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001124">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001124">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Synthesis of the lactone of (±)-α-(2-hydroxy-4-methyl-5-oxocycloheptyl)propionic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhanot</surname>
<given-names>Opinder Singh</given-names></name>
<name><surname>Mahajan</surname>
<given-names>Jaswant Rai</given-names></name>
<name><surname>Dutta</surname>
<given-names>Phanindra Chandra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1128</fpage>
<lpage>1134</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. 2- and 3-Amino-5α-androstanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001134</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1134</fpage>
<lpage>1140</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001134">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001134">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 derivatives of some flavan-3,4-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001140</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drewes</surname>
<given-names>S. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1140</fpage>
<lpage>1148</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001140">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001140">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phototransformations of tropolones. Part VI. New rearrangements in the benztropone series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001149</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>
<name><surname>Ripley</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1149</fpage>
<lpage>1152</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001149">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001149">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. 4-Substituted amino-cinnolines as potential antiprotozoal agents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001152</article-id><contrib-group><contrib contrib-type="author">
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1152</fpage>
<lpage>1155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001152">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001152">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. 4-Mercaptocinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001156</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1156</fpage>
<lpage>1158</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Naphthalene dichloride and its derivatives. Part I. The preparation and structure of a 1,2,3,4,8-pentachloro-1,2-dihydronaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001159</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1159</fpage>
<lpage>1162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001159">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001159">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure and stereochemistry of the hexahydroisochromanone from the carvenone–benzaldehyde condensation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001162</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>C. A. R.</given-names></name>
<name><surname>Forward</surname>
<given-names>G. C.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1162</fpage>
<lpage>1168</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001162">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001162">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the chemistry of the hexahydroisochromanone from the carvenone–benzaldehyde condensation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001169</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>C. A. R.</given-names></name>
<name><surname>Forward</surname>
<given-names>G. C.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1169</fpage>
<lpage>1173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001169">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001169">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry and structure in the tetrahydro-1-thio-4-pyrone and tetrahydro-4-pyrone series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001174</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>C. A. R.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1174</fpage>
<lpage>1178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001174">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001174">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 capaurimine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001178</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Yagi</surname>
<given-names>H.</given-names></name>
<name><surname>Iida</surname>
<given-names>H.</given-names></name>
<name><surname>Kikuchi</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1178</fpage>
<lpage>1180</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001178">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001178">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XXXV. The structure of the hydrated dimer formed by the action of dilute acid on 4-methylpteridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001181</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Yamamoto</surname>
<given-names>Hiroshi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1181</fpage>
<lpage>1187</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001181">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001181">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 aromatic systems. Part V. 5′-Hydroxy- and 5′-methoxy-benzocycloheptatrien-4′-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001187</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
<name><surname>Renfrew</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1187</fpage>
<lpage>1192</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001187">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001187">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 hop constituents. Part XXXII. Further studies on the oxidation of hop α-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001193</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connett</surname>
<given-names>B. E.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1193</fpage>
<lpage>1195</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001193">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001193">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Perfluoroacyl thiophens. Part I. The behaviour of 2-thienyl metals with perfluoroaliphatic acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001195</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1195</fpage>
<lpage>1196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001195">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001195">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclopropano-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001197</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>D. E.</given-names></name>
<name><surname>Lewis</surname>
<given-names>G. S.</given-names></name>
<name><surname>Palmer</surname>
<given-names>P. J.</given-names></name>
<name><surname>Weyell</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1197</fpage>
<lpage>1202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001197">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001197">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The preparation of some analogues of vitamin B&lt;sub&gt;6&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001203</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1203</fpage>
<lpage>1208</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001203">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001203">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structural biochemistry. Part VIII. 9-Amino-(9-deoxy)-cinchona alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001208</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pettit</surname>
<given-names>G. R.</given-names></name>
<name><surname>Gupta</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1208</fpage>
<lpage>1213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001208">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001208">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Halogeno-1,4-dioxans and their derivatives. Part IV. Some 2,3-disubstituted &lt;i&gt;cis&lt;/i&gt;-1,4,5,8-tetraoxadecalins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bramley</surname>
<given-names>R.</given-names></name>
<name><surname>Cort</surname>
<given-names>L. A.</given-names></name>
<name><surname>Pearson</surname>
<given-names>Ronald G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1213</fpage>
<lpage>1215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic analogues of polynucleotides. Part II. Studies on copolymers of 5′-&lt;i&gt;O&lt;/i&gt;-acryloyluridine with acrylamide and their interaction with deoxyribonucleic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001216</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>M. G.</given-names></name>
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1216</fpage>
<lpage>1218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001216">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001216">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIX. The use of &lt;i&gt;S&lt;/i&gt;-benzylthiomethyl-L-cysteine in peptide synthesis: synthesis of glutathione and homoglutathione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001219</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Camble</surname>
<given-names>R.</given-names></name>
<name><surname>Purkayastha</surname>
<given-names>R.</given-names></name>
<name><surname>Young</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1219</fpage>
<lpage>1224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001219">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001219">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XL. The preparation and some nucleophilic replacement reactions of 4,5,6,7-tetrafluorobenzo(&lt;i&gt;b&lt;/i&gt;)-thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Castle</surname>
<given-names>M. D.</given-names></name>
<name><surname>Plevey</surname>
<given-names>R. G.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1225</fpage>
<lpage>1227</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. The addition of thiols to 1,2,3,4,7,7-hexachloro-5,6-dimethylenenorborn-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001228</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alden</surname>
<given-names>C. K.</given-names></name>
<name><surname>Claisse</surname>
<given-names>J. A.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1228</fpage>
<lpage>1230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001228">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001228">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The deoxygenative chlorination of heterocyclic &lt;i&gt;S&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bird</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1230</fpage>
<lpage>1232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XL. Further reactions of diethyl fluoro-oxaloacetate with aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001232</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Shahak</surname>
<given-names>Israel</given-names></name>
<name><surname>Sal'i</surname>
<given-names>Etan</given-names></name>
<name><surname>Aizenshtat</surname>
<given-names>Zeev</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1232</fpage>
<lpage>1235</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001232">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001232">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in the indole series. Part IV. Tetrahydro-1&lt;i&gt;H&lt;/i&gt;-pyrido[4,3-&lt;i&gt;b&lt;/i&gt;]-indoles as serotonin antagonists</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001235</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cattanach</surname>
<given-names>C. J.</given-names></name>
<name><surname>Cohen</surname>
<given-names>A.</given-names></name>
<name><surname>Heath-Brown</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1235</fpage>
<lpage>1243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 indole in an attempted cyclisation of &lt;i&gt;o&lt;/i&gt;-nitrophenylsuccinic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001243</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Askam</surname>
<given-names>V.</given-names></name>
<name><surname>Deeks</surname>
<given-names>R. H. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1243</fpage>
<lpage>1245</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001243">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001243">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and optical rotatory dispersion of steroid 3-ethylenedithio-4-ketones and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001245</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robinson</surname>
<given-names>C. H.</given-names></name>
<name><surname>Milewich</surname>
<given-names>L.</given-names></name>
<name><surname>Snatzke</surname>
<given-names>G.</given-names></name>
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Wallis</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1245</fpage>
<lpage>1251</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 some highly substituted pyridines, 2,7-naphthyridines and 1&lt;i&gt;H&lt;/i&gt;-pyrimido[4,5,6-&lt;i&gt;i&lt;/i&gt;,&lt;i&gt;j&lt;/i&gt;][2,7]naphthyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001252</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>J. D.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1252</fpage>
<lpage>1258</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001252">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001252">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 deuterioporphyrin IX, pemptoporphyrin, and spirographis porphyrin dimethyl esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001259</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bamfield</surname>
<given-names>P.</given-names></name>
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Kenyon</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1259</fpage>
<lpage>1265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001259">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001259">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 arenesulphonyl chlorides from Grignard reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhattacharya</surname>
<given-names>S. N.</given-names></name>
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Walton</surname>
<given-names>D. R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1265</fpage>
<lpage>1267</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Halogeno-&lt;i&gt;o&lt;/i&gt;-phenylenediamines and derived heterocycles. Part I. Reductive fission of benzotriazoles to &lt;i&gt;o&lt;/i&gt;-phenylenediamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001268</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burton</surname>
<given-names>D. E.</given-names></name>
<name><surname>Lambie</surname>
<given-names>A. J.</given-names></name>
<name><surname>Lane</surname>
<given-names>D. W. J.</given-names></name>
<name><surname>Newbold</surname>
<given-names>G. T.</given-names></name>
<name><surname>Percival</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1268</fpage>
<lpage>1273</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Halogeno-&lt;i&gt;o&lt;/i&gt;-phenylenediamines and derived heterocycles. Part II. Hydrodechlorination of chloroquinoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001274</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burton</surname>
<given-names>D. E.</given-names></name>
<name><surname>Hughes</surname>
<given-names>D.</given-names></name>
<name><surname>Newbold</surname>
<given-names>G. T.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1274</fpage>
<lpage>1280</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001274">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001274">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The chemistry of some bromobenz[&lt;i&gt;b&lt;/i&gt;]azepines and the syntheis of an azatropone dimer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001280</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hannah</surname>
<given-names>E. D.</given-names></name>
<name><surname>Peaston</surname>
<given-names>W. C.</given-names></name>
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1280</fpage>
<lpage>1284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001280">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001280">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 leucoquinizarins with alkylenediamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001284</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greenhalgh</surname>
<given-names>C. W.</given-names></name>
<name><surname>Hughes</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1284</fpage>
<lpage>1288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001284">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001284">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>exo-2-Hydroxyepicamphor</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001289</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>Ian</given-names></name>
<name><surname>Woodward</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1289</fpage>
<lpage>1291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001289">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001289">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkylations and thermal sigmatropic rearrangements of nickel 1-methyl-tetradehydrocorrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001291</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grigg</surname>
<given-names>R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Shelton</surname>
<given-names>K. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1291</fpage>
<lpage>1296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001291">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001291">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 imines and amines. Part XI. Reactions of &lt;i&gt;o&lt;/i&gt;-cyanocinnamonitriles and related compounds with nitrogen bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001297</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1297</fpage>
<lpage>1300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001297">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001297">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carrageenans. Part VI. Reinvestigation of the acetolysis products of λ-carrageenan, revision of the structure of ‘α-1,3-galactotriose,’ and a further example of the reverse specificities of glycoside hydrolysis and acetolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001301</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawson</surname>
<given-names>C. J.</given-names></name>
<name><surname>Rees</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1301</fpage>
<lpage>1304</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001301">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001301">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The circular dichroism and optical rotatory dispersion of protoberberines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001305</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1305</fpage>
<lpage>1310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis of aryloxyacetones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dirania</surname>
<given-names>M. K. M.</given-names></name>
<name><surname>Hill</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1311</fpage>
<lpage>1316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 induction and configurational correlations in oxidations at sulphur. Part III. Oxidations of aryl alkyl sulphides to sulphoxides by optically active peroxy-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Folli</surname>
<given-names>U.</given-names></name>
<name><surname>Iarossi</surname>
<given-names>D.</given-names></name>
<name><surname>Montanari</surname>
<given-names>F.</given-names></name>
<name><surname>Torre</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1317</fpage>
<lpage>1322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Apetalactone, a new triterpene lactone from &lt;i&gt;Calophyllum&lt;/i&gt; species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Govindachari</surname>
<given-names>T. R.</given-names></name>
<name><surname>Prakash</surname>
<given-names>D.</given-names></name>
<name><surname>Viswanathan</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1323</fpage>
<lpage>1324</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrosoacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001324</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robson</surname>
<given-names>E.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
<name><surname>Woodcock</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1324</fpage>
<lpage>1328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001324">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001324">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 1-aryl 1,2,3-triazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Mansour</surname>
<given-names>H. A. R.</given-names></name>
<name><surname>Meshreki</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1329</fpage>
<lpage>1331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 sodium hydride with ω-hydroxyalkyl-phosphonium, -arsonium and -ammonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001331</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1331</fpage>
<lpage>1337</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 &lt;i&gt;NN&lt;/i&gt;-di-(2-chloroethyl)[3,5-&lt;sup&gt;3&lt;/sup&gt;H&lt;sub&gt;2&lt;/sub&gt;]aniline of high specific activity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001338</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ball</surname>
<given-names>C. R.</given-names></name>
<name><surname>Wade</surname>
<given-names>Roy</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1338</fpage>
<lpage>1339</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001338">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001338">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition of sulphenyl chlorides to acetylenes. Part VII. Factors affecting the orientation of the addition</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calo'</surname>
<given-names>V.</given-names></name>
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Scorrano</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1339</fpage>
<lpage>1344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition of sulphenyl chlorides to acetylenes. Part VIII. Effect of acids on the orientation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calo'</surname>
<given-names>V.</given-names></name>
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Scorrano</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1344</fpage>
<lpage>1347</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and structure of phorbol, the diterpene parent of the co-carcinogens of croton oil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>M. L.</given-names></name>
<name><surname>Pointer</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1347</fpage>
<lpage>1362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001347">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Pyrolysis, absolute configuration, and optical rotatory dispersion of steroidal methyl sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001362</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>
<name><surname>Saeed</surname>
<given-names>M. A.</given-names></name>
<name><surname>Whitehouse</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1362</fpage>
<lpage>1372</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001362">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001362">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 induction and configurational correlations in oxidations at sulphur. Part IV. Oxidation of aryl alkyl sulphoxides to sulphones by optically active peroxy-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001372</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Folli</surname>
<given-names>U.</given-names></name>
<name><surname>Iarossi</surname>
<given-names>D.</given-names></name>
<name><surname>Montanari</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1372</fpage>
<lpage>1374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001372">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001372">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Addition–cyclisations of ethoxycarbonylhydrazine and carbodi-imides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001375</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1375</fpage>
<lpage>1380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part V. Reaction of 2,3-&lt;i&gt;O&lt;/i&gt;-isopropylidene-5-&lt;i&gt;O&lt;/i&gt;-methylsulphonyl-D-lyxofuranose with sodium methoxide: aldehyde-group participation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001381</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Hunedy</surname>
<given-names>F.</given-names></name>
<name><surname>Tucker</surname>
<given-names>L. C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1381</fpage>
<lpage>1384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001381">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001381">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVII. Synthesis of five heptadecapeptides related to human gastrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Agarwal</surname>
<given-names>K. L.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1384</fpage>
<lpage>1391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A synthesis of 2,6-diacetyldeuterioporphyrin II dimethyl ester</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Janette L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1392</fpage>
<lpage>1396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001392">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 4-acetyl-oxazoles and the corresponding acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allan</surname>
<given-names>A. W.</given-names></name>
<name><surname>Walter</surname>
<given-names>B. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1397</fpage>
<lpage>1399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 δ-aminolaevulinic acid analogues as potential antimalarial agents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001399</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Salerni</surname>
<given-names>O. L.</given-names></name>
<name><surname>Smart</surname>
<given-names>B. E.</given-names></name>
<name><surname>Post</surname>
<given-names>A.</given-names></name>
<name><surname>Cheng</surname>
<given-names>C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1399</fpage>
<lpage>1401</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001399">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001399">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isothiazoles. Part XII. Isothiazole analogues of phenothiazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001402</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caton</surname>
<given-names>M. P. L.</given-names></name>
<name><surname>Slack</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1402</fpage>
<lpage>1404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001402">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001402">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 phospholipids. Part I. Phosphatidyl and lysophosphatidyl ethanolamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Billimoria</surname>
<given-names>J. D.</given-names></name>
<name><surname>Lewis</surname>
<given-names>K. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1404</fpage>
<lpage>1412</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3-Hydroxy-2-methyl-and 3-hydroxy-2,4-dimethyl-substituted long-chain carboxylic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001412</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coles</surname>
<given-names>Lydia</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1412</fpage>
<lpage>1419</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001412">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001412">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyanions and their complexes. Part III. Reactions of heparin, hyaluronic acid, sodium poly(ethylenesulphonate), sodium poly(styrenesulphonate), and sodium carboxymethylcellulose with hydroxyl radicals and hydrated electrons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Balazs</surname>
<given-names>E. A.</given-names></name>
<name><surname>Davies</surname>
<given-names>J. V.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. O.</given-names></name>
<name><surname>Scheufele</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1420</fpage>
<lpage>1423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyanions and their complexes. Part IV. A pulse radiolysis study of the interaction between methylene blue and heparin in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001424</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Balazs</surname>
<given-names>E. A.</given-names></name>
<name><surname>Davies</surname>
<given-names>J. V.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. O.</given-names></name>
<name><surname>Scheufele</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1424</fpage>
<lpage>1429</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001424">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001424">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyanions and their complexes. Part V. Examination of polyanion–cation interaction using pulse radiolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001429</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Balazs</surname>
<given-names>E. A.</given-names></name>
<name><surname>Davies</surname>
<given-names>J. V.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. O.</given-names></name>
<name><surname>Scheufele</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1429</fpage>
<lpage>1433</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001429">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001429">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. The oxidation products of some polymethoxyphenols, and the mechanism of demethylation in neutral solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001434</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adderley</surname>
<given-names>C. J. R.</given-names></name>
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1434</fpage>
<lpage>1438</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001434">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001434">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 alkoxphenols. Part XIII. Oxidation of t-butylated resorcinol monoethers and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001438</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adderley</surname>
<given-names>C. J. R.</given-names></name>
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1438</fpage>
<lpage>1443</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001438">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001438">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Thermal rearrangements of some aryloxycyclohexadienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adderley</surname>
<given-names>C. J. R.</given-names></name>
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1443</fpage>
<lpage>1445</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arylazo-steroids. Part III. 3-, 7-, and 17-Arylazo-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001445</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1445</fpage>
<lpage>1451</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001445">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001445">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrimidine reactions. Part XVII. Ring fission of 1,2-dihydro-2-imino-1-methyl-, 5-methylsulphonyl-, and 5-methylsulphinyl-pyrimidine by amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001452</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>Paddon-Row</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1452</fpage>
<lpage>1454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic analogues of polynucleotides. Part III. The synthesis and polymerisation of 2′,3′-&lt;i&gt;O&lt;/i&gt;-isopropylidene-5′-&lt;i&gt;O&lt;/i&gt;-(3-vinylacryloyl)uridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Khan</surname>
<given-names>M. K. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1454</fpage>
<lpage>1457</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Protein–carbohydrate interaction. Part XIV. Carbohydrates containing groups for the alkylation of proteins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001457</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buss</surname>
<given-names>D. H.</given-names></name>
<name><surname>Goldstein</surname>
<given-names>I. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1457</fpage>
<lpage>1461</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001457">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001457">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 formation of benzoxazoline derivatives from aminated quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001461</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Giles</surname>
<given-names>R. G. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1461</fpage>
<lpage>1464</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001461">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001461">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001465</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Nassr</surname>
<given-names>M. A. M.</given-names></name>
<name><surname>Shaban</surname>
<given-names>M. A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1465</fpage>
<lpage>1467</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001465">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001465">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. The photochemical reduction of nitro-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001467</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1467</fpage>
<lpage>1474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001467">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001467">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. The stereochemistry of the oxidative and hydrolytic cleavage of the 1-phenylethyl–boron bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001474</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Roberts</surname>
<given-names>B. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1474</fpage>
<lpage>1478</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001474">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001474">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Addition reactions catalysed by organolead compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001479</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1479</fpage>
<lpage>1483</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001479">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001479">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry of β-carboxy- and β-hydroxymethyl-muconic derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001483</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainsworth</surname>
<given-names>A. T.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1483</fpage>
<lpage>1487</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001483">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001483">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-[4,3-&lt;i&gt;b&lt;/i&gt;]- and [3,4-&lt;i&gt;c&lt;/i&gt;]-pyridines. Reactions of 2- and 4-bromomethyl-3-nitropyridine with aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001487</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hurst</surname>
<given-names>J.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1487</fpage>
<lpage>1490</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001487">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001487">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bicyclononanes. Part IV. 2-Dialkylaminobicyclononan-9-ols and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001491</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>C. S.</given-names></name>
<name><surname>Dixon</surname>
<given-names>J. R.</given-names></name>
<name><surname>Graham</surname>
<given-names>S. H.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1491</fpage>
<lpage>1494</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001491">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001491">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The synthesis of the fourteen-membered cyclodepsipeptides D-D-, L-L-, and D-L-cyclodi-(β-seryloxypropionyl)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001495</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Thomas</surname>
<given-names>Jean O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1495</fpage>
<lpage>1501</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001495">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001495">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation and chemical properties of 3-acyl-5-arylidene-4-hydroxy-2,5-dihydro-2-oxothiophens, a new class of immunosuppressive agent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001501</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Mant</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1501</fpage>
<lpage>1505</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001501">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001501">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 thebainone-A enol methyl ether with benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1506</fpage>
<lpage>1507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cycloaddition reactions of 2,2,2-trifluorodiazoethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001507</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1507</fpage>
<lpage>1513</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Schiff bases. Part III. Amine and ketone exchange reactions with Schiff bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawson</surname>
<given-names>Alexander</given-names></name>
<name><surname>Stevens</surname>
<given-names>J. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1514</fpage>
<lpage>1515</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVIII. Syntheses of 9-β-D-ribofuranosylzeatin 5′-phosphate, a naturally occurring adenylic acid derivative with plant cell-division promoting activity, and a new synthesis of 6-chloro-9-β-D-ribofuranosylpurine 5′-phosphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001516</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
<name><surname>Smallwood</surname>
<given-names>B. M.</given-names></name>
<name><surname>Wilson</surname>
<given-names>D. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1516</fpage>
<lpage>1519</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001516">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001516">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIX. Some reactions of &lt;i&gt;N&lt;/i&gt;-acetyl-&lt;i&gt;N&lt;/i&gt;′-(β-ethoxyacryloyl)ureas leading to uracils, aminopyrazoles and pyrazolo[3,4-&lt;i&gt;d&lt;/i&gt;]pyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lees</surname>
<given-names>P.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1519</fpage>
<lpage>1521</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Thiazoline-4-carboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001522</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1522</fpage>
<lpage>1526</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001522">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001522">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Experiments on the dehydrogenation of some thiazolines derived from cysteine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001526</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fuller</surname>
<given-names>N. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1526</fpage>
<lpage>1529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001526">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001526">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVIII. The structure and biosynthesis of &lt;i&gt;Erythrina&lt;/i&gt; alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>James</surname>
<given-names>R.</given-names></name>
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
<name><surname>Turner</surname>
<given-names>D. W.</given-names></name>
<name><surname>Widdowson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1529</fpage>
<lpage>1537</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polychloroaromatic compounds. Part I. Oxidation of pentachloropyridine and its &lt;i&gt;NN&lt;/i&gt;-disubstituted amino-derivatives with peroxyacids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001537</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roberts</surname>
<given-names>S. M.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1537</fpage>
<lpage>1541</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001537">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001537">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mycolipanolic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001541</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coles</surname>
<given-names>Lydia</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1541</fpage>
<lpage>1544</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001541">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001541">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIX. Reactions of mono- and di-methoxybiphenylenes and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001545</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>
<name><surname>Watts</surname>
<given-names>M. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1545</fpage>
<lpage>1549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. Autoxidation of 2- and 3-mono- and 2,5-di-t-butyl-4-methoxyphenol and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001549</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
<name><surname>Lee</surname>
<given-names>S. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1549</fpage>
<lpage>1556</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001549">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001549">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. The reaction of 4-methoxy-2,5-di-t-butylphenol with lead tetra-acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001556</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
<name><surname>Lee</surname>
<given-names>S. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1556</fpage>
<lpage>1558</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001556">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001556">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tetracycline studies. Part I. The selective oxidation of 6-methylpretetramid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001558</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1558</fpage>
<lpage>1560</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001558">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001558">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Synthesis of and nucleophilic substitution in octafluorodibenzofuran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001560</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>
<name><surname>Spring</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1560</fpage>
<lpage>1565</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-&lt;sup&gt;14&lt;/sup&gt;C]abscisic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cornforth</surname>
<given-names>J. W.</given-names></name>
<name><surname>Mallaby</surname>
<given-names>R.</given-names></name>
<name><surname>Ryback</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1565</fpage>
<lpage>1568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XLI. Some reactions of pentafluorobenzaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001569</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroskar</surname>
<given-names>(the late) E. V.</given-names></name>
<name><surname>Brown</surname>
<given-names>P. J. N.</given-names></name>
<name><surname>Plevey</surname>
<given-names>R. G.</given-names></name>
<name><surname>Stephens</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1569</fpage>
<lpage>1575</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001569">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001569">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The photocyclisation of some nuclear-substituted stilbenes to substituted phenanthrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001576</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackburn</surname>
<given-names>E. V.</given-names></name>
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1576</fpage>
<lpage>1580</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001576">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001576">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXI. Attempted modification of the 14α-methyl group in 4,4,14α-trimethyl steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001581</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Coll</surname>
<given-names>J. C.</given-names></name>
<name><surname>Lack</surname>
<given-names>Ruth E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1581</fpage>
<lpage>1585</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001581">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001581">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LII. Tri- and tetra-peptides of leucine and their protected derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001585</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dunstan</surname>
<given-names>D. R.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1585</fpage>
<lpage>1592</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001585">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001585">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>12-Aminoacetyl-12&lt;i&gt;H&lt;/i&gt;-benzo[&lt;i&gt;b&lt;/i&gt;]phenothiazine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001592</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jackson</surname>
<given-names>T. G.</given-names></name>
<name><surname>Morris</surname>
<given-names>S. R.</given-names></name>
<name><surname>Turner</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1592</fpage>
<lpage>1593</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001592">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001592">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-substituted-4&lt;i&gt;H&lt;/i&gt;-3,1-benzoxazin-4-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bain</surname>
<given-names>D. I.</given-names></name>
<name><surname>Smalley</surname>
<given-names>R. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1593</fpage>
<lpage>1597</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of &lt;i&gt;ortho&lt;/i&gt;-benzoquinones. Part I. Cycloaddition reactions with cyclic 1,3-dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001597</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Horspool</surname>
<given-names>W. M.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
<name><surname>Din</surname>
<given-names>Zia ud</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1597</fpage>
<lpage>1601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001597">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001597">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 3-diazo-2,4,5-triphenylpyrrole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001601</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartholomew</surname>
<given-names>R. F.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1601</fpage>
<lpage>1601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001601">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001601">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The interaction of toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl azide and some β-keto-sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001602</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hodson</surname>
<given-names>D.</given-names></name>
<name><surname>Holt</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1602</fpage>
<lpage>1603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001602">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001602">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vilsmeier adducts of dimethylformamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001603</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1603</fpage>
<lpage>1609</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Structure revision of a so-called phosphole. A stable alkylidene-1,6-diphosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001609</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1609</fpage>
<lpage>1612</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001609">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001609">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phenylsulphine and phenylsulphene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001612</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1612</fpage>
<lpage>1615</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001612">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001612">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,6-Addition of t-butylmagnesium chloride to anthraquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001615</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Meckel</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1615</fpage>
<lpage>1619</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001615">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001615">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Racemisation. Part II. Racemisation of 1-benzyltetrahydroisoquinolines under the conditions of catalytic hydrogenation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001619</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Ihara</surname>
<given-names>M.</given-names></name>
<name><surname>Shima</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1619</fpage>
<lpage>1620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001619">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001619">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fulvenes and thermochromic ethylenes. Part L. The reaction of diphenylcyclopropenone with (2-naphthylmethylene)triphenylphosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Agranat</surname>
<given-names>Israel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1621</fpage>
<lpage>1623</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXVI. Dialkyl acetylenedicarboxylates with 2-substituted benzimidazoles, benzoxazoles and benzothiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001623</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Tully</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1623</fpage>
<lpage>1629</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001623">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001623">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXVII. Dimethyl acetylenedicarboxylate with some substituted pyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Robinson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1629</fpage>
<lpage>1633</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXVIII. Cycl[3,2,2]azines and indolizines from pyridines and methyl propiolate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001633</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Robinson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1633</fpage>
<lpage>1638</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001633">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001633">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and some properties of 2-aminoethyl β-D-glucopyranoside</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Graham</surname>
<given-names>E. R. B.</given-names></name>
<name><surname>Neuberger</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1638</fpage>
<lpage>1641</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part VI. The solvolysis of methyl 2,3-di-&lt;i&gt;O&lt;/i&gt;-benzyl-6-&lt;i&gt;O&lt;/i&gt;-methylsulphonyl-β-D-galactopyranoside: participation by a benzyloxy-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Ching</surname>
<given-names>O. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1642</fpage>
<lpage>1646</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Epoxidation of allylic alcohols with chromium trioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001646</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glotter</surname>
<given-names>E.</given-names></name>
<name><surname>Greenfield</surname>
<given-names>S.</given-names></name>
<name><surname>Lavie</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1646</fpage>
<lpage>1653</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001646">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001646">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The reaction of dimethylketen with heteroaromatic &lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001653</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1653</fpage>
<lpage>1657</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Adamantane chemistry. Part I. The synthesis of 1,2-disubstituted adamantanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001657</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lunn</surname>
<given-names>W. H. W.</given-names></name>
<name><surname>Podmore</surname>
<given-names>W. D.</given-names></name>
<name><surname>Szinai</surname>
<given-names>S. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1657</fpage>
<lpage>1660</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001657">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001657">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereochemistry of some halogeno-derivatives of aucubin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001661</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Quesne</surname>
<given-names>P. W. Le</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1661</fpage>
<lpage>1663</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001661">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001661">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzocyclo-octatetraenes. Part II. Nitro derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001663</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1663</fpage>
<lpage>1667</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001663">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001663">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 reactions of indolenines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Smith</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1667</fpage>
<lpage>1675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The rearrangements of 1,4-disubstituted 4-chloromethyl-3,5-dicyano-2,6-dimethyl-1,4-dihydropyridines to 1,4-disubstituted 3,6-dicyano-2,7-dimethyl-1&lt;i&gt;H&lt;/i&gt;-azepines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001675</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gill</surname>
<given-names>G. B.</given-names></name>
<name><surname>Harper</surname>
<given-names>D. J.</given-names></name>
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1675</fpage>
<lpage>1683</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001675">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001675">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Stereospecific synthesis of benzylic centres. Some 6-deoxy-5-&lt;i&gt;C&lt;/i&gt;-phenylhexose derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001683</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Inch</surname>
<given-names>T. D.</given-names></name>
<name><surname>Ley</surname>
<given-names>R. V.</given-names></name>
<name><surname>Rich</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1683</fpage>
<lpage>1692</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001683">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001683">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. Stereospecific synthesis of (&lt;i&gt;R&lt;/i&gt;)-2-hydroxy-2-phenylpropionic acid, and (&lt;i&gt;R&lt;/i&gt;)- and (&lt;i&gt;S&lt;/i&gt;)-2-cyclohexyl-2-hydroxy-2-phenylacetic acid. Configurational relationship between (&lt;i&gt;R&lt;/i&gt;)(–)-2-hydroxy-2-phenylpropionic acid and (&lt;i&gt;S&lt;/i&gt;)(+)-2-phenylpropionic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001693</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Inch</surname>
<given-names>T. D.</given-names></name>
<name><surname>Ley</surname>
<given-names>R. V.</given-names></name>
<name><surname>Rich</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1693</fpage>
<lpage>1699</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001693">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001693">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 tetraphenyldiphosphine with aliphatic carboxylic acids and with aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001700</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1700</fpage>
<lpage>1703</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001700">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001700">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The use of aminomagnesium compounds in the preparation of α-amino-acid amides from α-amino-acid ethyl esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001704</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blažević</surname>
<given-names>K.</given-names></name>
<name><surname>Houghton</surname>
<given-names>R. P.</given-names></name>
<name><surname>Williams</surname>
<given-names>C. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1704</fpage>
<lpage>1708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001704">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001704">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dimers, and benz[&lt;i&gt;d&lt;/i&gt;,&lt;i&gt;e&lt;/i&gt;]isoquinolines from 4-phenacylidenehomophthalimides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001709</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>Bell</surname>
<given-names>P. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1709</fpage>
<lpage>1710</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001709">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 substituted 2-alkyl-2&lt;i&gt;H&lt;/i&gt;-tetrazol-5-ylhydrazones with bromine and lead tetra-acetate: routes to 6-aryl-1-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/J39680001711</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1711</fpage>
<lpage>1716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001711">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001711">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The solvolytic behaviour of &lt;i&gt;exo&lt;/i&gt;- and &lt;i&gt;endo&lt;/i&gt;-bicyclo[3,2,1]octane-6-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Appleton</surname>
<given-names>R. A.</given-names></name>
<name><surname>Fairlie</surname>
<given-names>J. C.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Parker</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1716</fpage>
<lpage>1721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001716">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclisations of &lt;i&gt;o&lt;/i&gt;-substituted anilines and benzoic acids with manganese dioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001722</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meth-Cohn</surname>
<given-names>O.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
<name><surname>Sutton</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1722</fpage>
<lpage>1726</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001722">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001722">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;vic&lt;/i&gt;-Enediamines. Reaction of some tert-β-dichloroalkylamines with lithium-dialkylamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Halleux</surname>
<given-names>A.</given-names></name>
<name><surname>Viehe</surname>
<given-names>H. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1726</fpage>
<lpage>1730</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001726">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 aspects of the chemistry of &lt;i&gt;N&lt;/i&gt;(1)- and &lt;i&gt;N&lt;/i&gt;(6)-dimethylallyl derivatives of adenosine and adenine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001731</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>D. M. G.</given-names></name>
<name><surname>Reese</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1731</fpage>
<lpage>1738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001731">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001731">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphonohydrazides and related compounds. Part IX. The ultraviolet spectra of some related aromatic sulphonamides, sulphonohydrazides, acetone sulphonohydrazones, and sulphonyl azides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001738</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
<name><surname>Pryce-Jones</surname>
<given-names>T.</given-names></name>
<name><surname>Swinbourne</surname>
<given-names>F. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1738</fpage>
<lpage>1739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001738">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001738">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transformations of steroidal neopentyl systems. Part IV. Stereochemistry of products of reaction of methyl-lithium with Δ&lt;sup&gt;5&lt;/sup&gt;-19-aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001740</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wicha</surname>
<given-names>J.</given-names></name>
<name><surname>Caspi</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1740</fpage>
<lpage>1746</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001740">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001740">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amination of &lt;i&gt;NN&lt;/i&gt;′-dibenzenesulphonyl-1,4-benzoquinone di-imines: photochemical formation of benzimidazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>I.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1747</fpage>
<lpage>1752</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acid-catalysed ring-cleavage of some pyrimidine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001753</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrews</surname>
<given-names>K. J. M.</given-names></name>
<name><surname>Tong</surname>
<given-names>B. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1753</fpage>
<lpage>1761</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001753">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001753">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nitration of 3-methoxyfluoranthene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001761</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrew</surname>
<given-names>H. F.</given-names></name>
<name><surname>Campbell</surname>
<given-names>Neil</given-names></name>
<name><surname>Craig</surname>
<given-names>J. T.</given-names></name>
<name><surname>Nichol</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1761</fpage>
<lpage>1764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001761">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001761">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic replacement reactions of sulphonates. Part III. The synthesis of derivatives of 2,3,4,6-tetra-amino-2,3,4,6-tetradeoxy-D-galactose and -D-idose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001764</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ali</surname>
<given-names>Y.</given-names></name>
<name><surname>Richardson</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1764</fpage>
<lpage>1769</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001764">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001764">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 amino-acid and peptide derivatives. Part II. Phthaloylamino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001770</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Jones</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1770</fpage>
<lpage>1774</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001770">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001770">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 some α-acetylenic ketones and the related αβ-dibromoketones into 3,5-diarylisoxazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001774</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1774</fpage>
<lpage>1777</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001774">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001774">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reissert compounds. The reaction of some thiocarbonyl chlorides with quinoline, isoquinoline, and pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001777</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1777</fpage>
<lpage>1780</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001777">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001777">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 long-chain unsaturated fatty acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001781</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whitfield</surname>
<given-names>G. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1781</fpage>
<lpage>1784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001781">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001781">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 size and conformation of some (5&lt;i&gt;R&lt;/i&gt;)-5-&lt;i&gt;C&lt;/i&gt;-alkyl-5-&lt;i&gt;C&lt;/i&gt;-phenyl-D-xylose derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001784</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Inch</surname>
<given-names>T. D.</given-names></name>
<name><surname>Rich</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1784</fpage>
<lpage>1790</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001784">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001784">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Fluorescent derivatives of melphalan and other amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001791</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Everett</surname>
<given-names>J. L.</given-names></name>
<name><surname>Baker</surname>
<given-names>M. H.</given-names></name>
<name><surname>Bergel</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1791</fpage>
<lpage>1792</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001791">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001791">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Poly- and copoly-(amino-acyl) derivatives of melphalan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001792</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Szekerke</surname>
<given-names>(Miss) M.</given-names></name>
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1792</fpage>
<lpage>1795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001792">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001792">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Indoles from quinones: the synthesis of 1-alkyl 5-hydroxy-2-phenylindole derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001795</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Betkerur</surname>
<given-names>Suresh N.</given-names></name>
<name><surname>Siddappa</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1795</fpage>
<lpage>1797</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001795">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001795">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stebisimine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001798</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Kusama</surname>
<given-names>O.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1798</fpage>
<lpage>1800</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001798">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001798">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dihydropyran derivatives from the dimerisation of crotonaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001801</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1801</fpage>
<lpage>1802</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001801">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001801">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The total synthesis of dihydrocrinine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001802</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irie</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Uyeo</surname>
<given-names>Shojiro</given-names></name>
<name><surname>Yoshitake</surname>
<given-names>Akira</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1802</fpage>
<lpage>1804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001802">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001802">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. Evidence for electronically excited ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001805</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Ward</surname>
<given-names>S. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1805</fpage>
<lpage>1807</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001805">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001805">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 XVI. Further carbon-14 labelling studies relating to the biosynthesis of sulochrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001807</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Curtis</surname>
<given-names>R. F.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Pike</surname>
<given-names>R. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1807</fpage>
<lpage>1810</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001807">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001807">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 5-acetamido-5-deoxy-D-lyxopyranose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001811</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Hunedy</surname>
<given-names>F.</given-names></name>
<name><surname>Stacey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1811</fpage>
<lpage>1813</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001811">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001811">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 the biosynthesis of steroids and terpenoids. Part I. A preliminary study of the biosynthesis of santonin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001813</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Moss</surname>
<given-names>G. P.</given-names></name>
<name><surname>Whittle</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1813</fpage>
<lpage>1818</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001813">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001813">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cigarette smoke. Part XI. The isolation and synthesis of acenaphthylenes and macrocyclic polyolefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001818</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1818</fpage>
<lpage>1822</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Dehydration rearrangements of 7-hydroxyhopanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001823</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>
<name><surname>Young</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1823</fpage>
<lpage>1827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001823">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001823">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Limonoids from the timber of &lt;i&gt;Trichilia heudelottii&lt;/i&gt; Planch. ex Oliv.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001828</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Okorie</surname>
<given-names>D. A.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1828</fpage>
<lpage>1831</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001828">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001828">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The free-radical addition of thiophenol to bornylene and apobornylene: structures of product sulphides and sulphones formed on oxidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001832</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1832</fpage>
<lpage>1836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001832">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001832">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phosphate esters. Part I. The synthesis of phenolic isoprenoids from allylic phosphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001837</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>J. A.</given-names></name>
<name><surname>Wood</surname>
<given-names>H. C. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1837</fpage>
<lpage>1843</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001837">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001837">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;threo&lt;/i&gt;-β-Hydroxyaspartyl dipeptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001843</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>
<name><surname>Sokoloff</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1843</fpage>
<lpage>1845</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001843">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001843">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 spectra of 1-arylpyrazolemonocarboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001845</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>Hassan El</given-names></name>
<name><surname>Rateb</surname>
<given-names>Latif</given-names></name>
<name><surname>Mokhtar</surname>
<given-names>Hassan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1845</fpage>
<lpage>1848</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001845">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001845">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformation of the side chain in cortisone and related compounds; an infra red and nuclear magnetic resonance study</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001849</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cole</surname>
<given-names>W. G.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1849</fpage>
<lpage>1852</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001849">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001849">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The resolution of 2-(α-hydroxybenzyl)-1,4,5,6-tetrahydropyrimidines and a comparison of their optical rotary dispersion curves with those of related mandelic acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001853</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Neilson</surname>
<given-names>D. G.</given-names></name>
<name><surname>Khan</surname>
<given-names>I. A.</given-names></name>
<name><surname>Whitehead</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1853</fpage>
<lpage>1856</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001853">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001853">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The catalytic dimerisation of dienes by nitrosylcarbonyl transition-metal compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001856</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Candlin</surname>
<given-names>J. P.</given-names></name>
<name><surname>Janes</surname>
<given-names>W. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1856</fpage>
<lpage>1860</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001856">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001856">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 catalytic properties of the pentapeptide, Thr-Ala-Cys-His-Asp</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001860</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Photaki</surname>
<given-names>I.</given-names></name>
<name><surname>Bardakos</surname>
<given-names>V.</given-names></name>
<name><surname>Lake</surname>
<given-names>A. W.</given-names></name>
<name><surname>Lowe</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1860</fpage>
<lpage>1864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001860">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001860">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. The conversion of 5-arylvaleric acids into 1,2,3,4-tetrahydronaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001865</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1865</fpage>
<lpage>1869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001865">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001865">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 methanesulphonyl- and of certain arylsulphonyl-esters of hydroxyalkyl-substituted primary aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001869</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1869</fpage>
<lpage>1872</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001869">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001869">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 syntheses of sulphones from benzoyl peroxide and sulphur dioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001872</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corrêa</surname>
<given-names>C. M. M. da Silva</given-names></name>
<name><surname>Lindsay</surname>
<given-names>A. S.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1872</fpage>
<lpage>1874</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001872">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001872">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of the free toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl radical. Part I. Diagnostic reactions of free radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001874</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corrêa</surname>
<given-names>C. M. M. da Silva</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1874</fpage>
<lpage>1879</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001874">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001874">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of the free toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl radical. Part II. Reactions with polycyclic aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001880</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corrêa</surname>
<given-names>C. M. M. da Silva</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1880</fpage>
<lpage>1882</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001880">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001880">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and some rearrangements of 2-acetyl-4,6-diethyl-1,3,4-trihydroxycyclo-2,6-dien-5-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001882</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>S. J.</given-names></name>
<name><surname>Smith</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1882</fpage>
<lpage>1885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001882">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001882">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lignans and related phenols. Part VI. Synthesis of 2-aryltertrahydrooxofuran derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001885</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Mhasalkar</surname>
<given-names>S. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1885</fpage>
<lpage>1887</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001885">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001885">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 4,5,6,6&lt;i&gt;a&lt;/i&gt;,6&lt;i&gt;b&lt;/i&gt;,7,8,12&lt;i&gt;b&lt;/i&gt;-octahydrobenzo[&lt;i&gt;j&lt;/i&gt;]fluoranthene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001887</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>Neil</given-names></name>
<name><surname>Gorrie</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1887</fpage>
<lpage>1890</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001887">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001887">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 quaternary ammonium hydroxides. Part IV. Methohydroxides of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-2-alkyl-&lt;i&gt;NN&lt;/i&gt;-dimethylcyclohexylamines: evidence for elimination from a twist boat conformation.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001891</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>H.</given-names></name>
<name><surname>Franklin</surname>
<given-names>N. C.</given-names></name>
<name><surname>Gidley</surname>
<given-names>G. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1891</fpage>
<lpage>1894</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001891">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001891">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryne chemistry. Part XII. Some cycloaddition reactions of tetrachlorobenzyne</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
<name><surname>Jablonski</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1895</fpage>
<lpage>1898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 of auriculatin, extractive of &lt;i&gt;Milletia auriculata&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001899</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shabbir</surname>
<given-names>Mohammad</given-names></name>
<name><surname>Zaman</surname>
<given-names>Asif</given-names></name>
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Tuck</surname>
<given-names>B.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1899</fpage>
<lpage>1901</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001899">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001899">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Selective dibromination of adamantane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001902</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Talaty</surname>
<given-names>Erach R.</given-names></name>
<name><surname>Cancienne jun. </surname>
<given-names>Albert E.</given-names></name>
<name><surname>Dupuy jun. </surname>
<given-names>Aubry E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1902</fpage>
<lpage>1903</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001902">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001902">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The allyl ether as a protecting group in carbohydrate chemistry. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001903</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gigg</surname>
<given-names>Roy</given-names></name>
<name><surname>Warren</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1903</fpage>
<lpage>1911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001903">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001903">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Auto-oxidation of lanostenyl acetate: the major peroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001911</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scotney</surname>
<given-names>J.</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1911</fpage>
<lpage>1913</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001911">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001911">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 dimers of 4,6-di-t-butyl-3-hydroxy-&lt;i&gt;o&lt;/i&gt;-benzoquinone and 5-t-butyl-3-hydroxy-&lt;i&gt;o&lt;/i&gt;-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001914</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waldron</surname>
<given-names>N. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1914</fpage>
<lpage>1917</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001914">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001914">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The photochemistry and cycloaddition of a monocyclic α-dinitrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001917</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lamchen</surname>
<given-names>M.</given-names></name>
<name><surname>Mittag</surname>
<given-names>T. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1917</fpage>
<lpage>1921</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001917">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001917">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction between hydroxylamine and cytosine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001922</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hewlins</surname>
<given-names>M. J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1922</fpage>
<lpage>1924</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001922">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001922">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The tautomeric state of &lt;i&gt;N&lt;/i&gt;(4)-hydroxy- and of &lt;i&gt;N&lt;/i&gt;(4)-amino-cytosine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hewlins</surname>
<given-names>M. J. E.</given-names></name>
<name><surname>Schell</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1925</fpage>
<lpage>1929</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The formation of anomeric nucleosides from the silver salt of hypoxanthine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001929</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogers</surname>
<given-names>G. T.</given-names></name>
<name><surname>Ulbricht</surname>
<given-names>T. L. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1929</fpage>
<lpage>1933</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001929">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001929">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Some reactions of tetrafluoroisonicotinic acid and pentafluorobenzoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001933</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Heaton</surname>
<given-names>C. A.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1933</fpage>
<lpage>1937</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001933">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001933">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXI. Oxazoles from pyrolysis of aryl and heterocyclic azides in a mixture of acetic and polyphosphoric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001937</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1937</fpage>
<lpage>1940</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001937">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001937">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Modified anthraquinones from &lt;i&gt;Penicillium islandicum&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001941</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>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1941</fpage>
<lpage>1943</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazoline studies. Part XII. Action of acid and alkali on quinazoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001944</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Yamamoto</surname>
<given-names>Hiroshi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1944</fpage>
<lpage>1949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001944">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001944">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LIII. Diterpenecarboxylic acids and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001949</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Renwick</surname>
<given-names>J. D.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1949</fpage>
<lpage>1954</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001949">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001949">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LIV. Some D-homo-steroid lactones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001954</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>R. C.</given-names></name>
<name><surname>Turner</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1954</fpage>
<lpage>1957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001954">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001954">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXX. Some further syntheses of &lt;i&gt;N&lt;/i&gt;-glycyl-D-ribofuranosylamine 5-phosphate (GAR) and &lt;i&gt;N&lt;/i&gt;-(&lt;i&gt;N&lt;/i&gt;-formylglycyl)-D-ribofuranosylamine 5-phosphate (FGAR), intermediates in the biosynthesis &lt;i&gt;de novo&lt;/i&gt; of purine nucleotides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001957</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carrington</surname>
<given-names>R.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1957</fpage>
<lpage>1961</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001957">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001957">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metals in the synthesis of macrocycles. Part I. Metal complexes of 2,6-bis-(1-iminoisoindolin-3-ylideneamino)pyridine as templates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001961</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bamfield</surname>
<given-names>P.</given-names></name>
<name><surname>Mack</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1961</fpage>
<lpage>1964</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001961">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001961">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. The nitration of 2-chlorotropone: a new rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001964</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1964</fpage>
<lpage>1968</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001964">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001964">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. The mechanism of the production of &lt;i&gt;m&lt;/i&gt;-hydroxybenzaldehydes from 2-chlorotropones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001969</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>E. J.</given-names></name>
<name><surname>Gregory</surname>
<given-names>M. J.</given-names></name>
<name><surname>Warrell</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1969</fpage>
<lpage>1973</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001969">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001969">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Khaya senegalensis&lt;/i&gt;(Desr.) A. Juss</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001974</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adesogan</surname>
<given-names>E. K.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1974</fpage>
<lpage>1981</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001974">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001974">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;cis&lt;/i&gt;-2,&lt;i&gt;cis&lt;/i&gt;-4-vitamin A acid by a Wittig condensation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001982</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garbers</surname>
<given-names>C. F.</given-names></name>
<name><surname>Schneider</surname>
<given-names>D. F.</given-names></name>
<name><surname>Merwe</surname>
<given-names>J. P. van der</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1982</fpage>
<lpage>1983</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001982">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001982">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVIII. Synthesis of &lt;i&gt;cis&lt;/i&gt;- and di-&lt;i&gt;cis&lt;/i&gt;-polyenes by reactions of the Wittig type</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001984</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pattenden</surname>
<given-names>Gerald</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1984</fpage>
<lpage>1997</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001984">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001984">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIX. The geometrical isomers of 2- and 3-methyl-5-phenylpenta-2,4-dienoic acid and their methyl esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680001997</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pattenden</surname>
<given-names>Gerald</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1997</fpage>
<lpage>2006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680001997">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680001997">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pyrolysis. Part XXIV. Competitive routes in the pyrolysis of carboxylic acid anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>A. L.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2007</fpage>
<lpage>2013</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pyrolysis. Part XXV. Acrylic, methacrylic, and crotonic acid, and some derivatives: novel decarbonylation of αβ-unsaturated carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002013</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forman</surname>
<given-names>R. L.</given-names></name>
<name><surname>Mackinnon</surname>
<given-names>H. M.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2013</fpage>
<lpage>2016</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002013">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002013">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 pyrolysis. Part XXVI. Model systems for the pyrolysis of poly(ethylene fumarate) and allied polyesters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002016</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forman</surname>
<given-names>R. L.</given-names></name>
<name><surname>Mackinnon</surname>
<given-names>H. M.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2016</fpage>
<lpage>2023</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002016">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002016">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 aromatic systems. Part VI. Some aspects of the bromination of indane and 2,3-dimethylfluorenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002023</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2023</fpage>
<lpage>2025</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002023">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002023">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation and properties of some benzylated nucleosides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brookes</surname>
<given-names>P.</given-names></name>
<name><surname>Dipple</surname>
<given-names>A.</given-names></name>
<name><surname>Lawley</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2026</fpage>
<lpage>2028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Compounds derived from nitration of the halogeno-derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002028</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2028</fpage>
<lpage>2030</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 neutral plasmalogens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002030</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2030</fpage>
<lpage>2032</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bicyclononanes. Part V. Formation of substituted bicyclononanes from enamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Appleton</surname>
<given-names>R. A.</given-names></name>
<name><surname>Baggaley</surname>
<given-names>K. H.</given-names></name>
<name><surname>Egan</surname>
<given-names>Sister C.</given-names></name>
<name><surname>Davies</surname>
<given-names>(Miss) J. M.</given-names></name>
<name><surname>Graham</surname>
<given-names>S. H.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2032</fpage>
<lpage>2039</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bicyclononanes. Part VI. Bicyclo[3,3,1]nonenols and bicyclononanediols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>(Miss) J. M.</given-names></name>
<name><surname>Graham</surname>
<given-names>S. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2040</fpage>
<lpage>2041</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The alkaline degradation of deoxyribonucleic acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002042</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Mian</surname>
<given-names>A. M.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2042</fpage>
<lpage>2044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002042">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002042">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 structures of 1,2,3,4-tetrahydro-1,4-dioxopyrazino[1,2-&lt;i&gt;a&lt;/i&gt;]indoles from cultures of &lt;i&gt;Penicillium terlikowskii&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ali</surname>
<given-names>M. S.</given-names></name>
<name><surname>Shannon</surname>
<given-names>J. S.</given-names></name>
<name><surname>Taylor</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2044</fpage>
<lpage>2048</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 prototropic isomerization. Part V. A novel method for the preparation of enamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002048</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2048</fpage>
<lpage>2050</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dihydrocytosine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002050</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hewlins</surname>
<given-names>M. J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2050</fpage>
<lpage>2055</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002050">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002050">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Some reactions with cyclohexa-1,3-diene and cyclohexene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002055</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baggaley</surname>
<given-names>A. J.</given-names></name>
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2055</fpage>
<lpage>2059</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002055">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002055">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The formation of a xanthen derivative related to diduroquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002060</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Houghton</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2060</fpage>
<lpage>2064</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002060">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002060">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The function of quinone methides in the side-chain amination of alkylquinones and in dimerisations giving ethylenediquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002065</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2065</fpage>
<lpage>2069</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002065">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002065">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXI. The Skraup reaction with diamines derived from acenaphthene and anthracene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002070</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Dufour</surname>
<given-names>M.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2070</fpage>
<lpage>2072</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002070">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002070">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Monofluoroisoquinolines. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002073</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Belsten</surname>
<given-names>J. C.</given-names></name>
<name><surname>Dyke</surname>
<given-names>S. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2073</fpage>
<lpage>2075</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002073">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002073">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2,3,4,6-Penta-azaindenes (8-azapurines). Part IV. A new route to the 8-methyl-8-azapurines through the 2-methyl-1,2,3-triazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002076</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2076</fpage>
<lpage>2083</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002076">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002076">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXIII. Substitution reactions of the 5α-cholestan-4-ols: a further example of Walden retention</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002083</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>R. E.</given-names></name>
<name><surname>Sharma</surname>
<given-names>S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2083</fpage>
<lpage>2086</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. The adducts of dimethylketen with diarylnitrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002086</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pratt</surname>
<given-names>R. N.</given-names></name>
<name><surname>Stokes</surname>
<given-names>D. P.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. A.</given-names></name>
<name><surname>Brookes</surname>
<given-names>Miss P. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2086</fpage>
<lpage>2089</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002086">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002086">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 possible interconversion of phenylhydrazones and phenylazoalkanes. Part IV. Studies in deuteriated solvents: mechanism of the interconversion of &lt;i&gt;syn&lt;/i&gt;- and &lt;i&gt;anti&lt;/i&gt;-acetaldehyde phenylhydrazone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellamy</surname>
<given-names>A. J.</given-names></name>
<name><surname>Guthrie</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2090</fpage>
<lpage>2091</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Conformation in the 1,3,2-dioxaphosph(V)orinan series. Proton magnetic resonance assignments to &lt;i&gt;gem&lt;/i&gt;-5,5-dimethyl groups, and conformation at phosphorus</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002091</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Mitchell</surname>
<given-names>E. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2091</fpage>
<lpage>2094</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;o&lt;/i&gt;- and &lt;i&gt;p&lt;/i&gt;-Cyclopropylbenzaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002095</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harnden</surname>
<given-names>M. R.</given-names></name>
<name><surname>Rasmussen</surname>
<given-names>R. R.</given-names></name>
<name><surname>Baker</surname>
<given-names>(Mrs.) E. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2095</fpage>
<lpage>2096</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002095">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002095">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 bisarylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002097</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>El-Sadik</surname>
<given-names>M. M.</given-names></name>
<name><surname>Meshreki</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2097</fpage>
<lpage>2099</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002097">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002097">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. The interaction of thiocarbohydrazide and diarylcarbodi-imides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
<name><surname>Wilkinson</surname>
<given-names>Michael</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2099</fpage>
<lpage>2107</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. The hydrazinolysis of 4-substituted 1-dithiomethoxycarbonyl-3-thiosemicarbazides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002108</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
<name><surname>Wilkinson</surname>
<given-names>Michael</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2108</fpage>
<lpage>2111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002108">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002108">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azasteroids. Part II. 8-Aza-19-nortestosterones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002111</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowler (Mrs.) </surname>
<given-names>J.</given-names></name>
<name><surname>Clarkson</surname>
<given-names>R.</given-names></name>
<name><surname>Doyle</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2111</fpage>
<lpage>2115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002111">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002111">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyfluoro-heterocyclic compounds. Part XII. Preparation and nucleophilic substitution of tetrafluoropyridazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002116</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>MacBride</surname>
<given-names>J. A. H.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2116</fpage>
<lpage>2119</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002116">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002116">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 photochemical cyclisation of &lt;i&gt;o&lt;/i&gt;-bisiodoethynylbenzene to substituted naphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002120</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cambell</surname>
<given-names>I. D.</given-names></name>
<name><surname>Eglinton</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2120</fpage>
<lpage>2121</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002120">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002120">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6β-Hydroxyrosenonolactone: a new metabolite from &lt;i&gt;Trichothecium roseum&lt;/i&gt; link</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allison</surname>
<given-names>A. J.</given-names></name>
<name><surname>Connolly</surname>
<given-names>J. D.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2122</fpage>
<lpage>2125</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 derivatives of benzene-1,2,3,5-tetrol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002125</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2125</fpage>
<lpage>2128</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002125">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002125">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XLI. The reaction of hydrofluoric acid with cycloalkene epoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002129</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shahak</surname>
<given-names>I.</given-names></name>
<name><surname>Manor</surname>
<given-names>Sh.</given-names></name>
<name><surname>Bergmann</surname>
<given-names>E. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2129</fpage>
<lpage>2131</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002129">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002129">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVIII. Total synthesis of (±)-carabrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002131</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2131</fpage>
<lpage>2137</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydroxymethylene ketones. Part II. Other routes for the preparation of isoxazoles and pyrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002137</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rateb</surname>
<given-names>Latif</given-names></name>
<name><surname>Mina</surname>
<given-names>George Attalah</given-names></name>
<name><surname>Soliman</surname>
<given-names>Gabra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2137</fpage>
<lpage>2139</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002137">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002137">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 hydroxymethylene ketones. Part III. Synthesis of 1,2-dihydro-2-oxo-pyridine polycarboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002140</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rateb</surname>
<given-names>Latif</given-names></name>
<name><surname>Mina</surname>
<given-names>George Attalah</given-names></name>
<name><surname>Soliman</surname>
<given-names>Gabra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2140</fpage>
<lpage>2144</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002140">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002140">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of some indole derivatives with benzoyl nitrate. Novel oxidative coupling reactions of 2-methylindoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002145</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berti</surname>
<given-names>G.</given-names></name>
<name><surname>Settimo</surname>
<given-names>A. Da</given-names></name>
<name><surname>Nannipieri</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2145</fpage>
<lpage>2151</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002145">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002145">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002151</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2151</fpage>
<lpage>2154</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002151">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002151">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;m&lt;/i&gt;-Terphenyl-2- and -2′-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002154</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. H.</given-names></name>
<name><surname>Wragg</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2154</fpage>
<lpage>2155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002154">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002154">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 homoerythrinadienone by phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2156</fpage>
<lpage>2159</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrimidine reactions. Part XVIII. The conversion of 4-methoxy-5-nitropyrimidine into 3-amino-4-nitropyrazole by hydrazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002159</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>Porter</surname>
<given-names>Q. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2159</fpage>
<lpage>2162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002159">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002159">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. The biosynthesis of narcotine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Hirst</surname>
<given-names>M.</given-names></name>
<name><surname>McCaldin</surname>
<given-names>D. J.</given-names></name>
<name><surname>Southgate</surname>
<given-names>R.</given-names></name>
<name><surname>Staunton</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2163</fpage>
<lpage>2172</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 a dihydroxymethyl ketostearate from auto-oxidised methyl linoleate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002172</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Purdy</surname>
<given-names>S. Jean</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2172</fpage>
<lpage>2174</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002172">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002172">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arabinogalactan A from Japanese larch (&lt;i&gt;Larix leptolepis&lt;/i&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002174</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Fairweather</surname>
<given-names>R. M.</given-names></name>
<name><surname>Wood</surname>
<given-names>T. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2174</fpage>
<lpage>2179</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002174">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002174">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphonyl-stabilised sulphonium ylids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002180</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robson</surname>
<given-names>P.</given-names></name>
<name><surname>Speakman</surname>
<given-names>P. R. H.</given-names></name>
<name><surname>Stewart</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2180</fpage>
<lpage>2183</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002180">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002180">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Auto-oxidation of 7,11-dioxolanostenyl acetate: 1-Substituted derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002184</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scotney</surname>
<given-names>J.</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2184</fpage>
<lpage>2185</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002184">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002184">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Assignment of configurations to the 1,3,4,7-tetramethylisoindolines by use of nuclear magnetic resonance spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002186</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bender</surname>
<given-names>C. O.</given-names></name>
<name><surname>Bonnett</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2186</fpage>
<lpage>2188</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002186">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002186">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 syntheses with malonyl chloride. Part IX. 2-Substituted 4-chloro-6-pyrimidones from certain nitriles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002188</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Zaidi</surname>
<given-names>N. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2188</fpage>
<lpage>2198</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002188">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002188">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 some products from the electrolysis of cyclohexane-1,3-dione and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002199</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. H.</given-names></name>
<name><surname>Johnston</surname>
<given-names>K. M.</given-names></name>
<name><surname>Stride</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2199</fpage>
<lpage>2201</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002199">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002199">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>α-Diazosulphones and related compounds from the base-induced cleavage of α-diazo-β-ketosulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002201</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hodson</surname>
<given-names>D.</given-names></name>
<name><surname>Holt</surname>
<given-names>G.</given-names></name>
<name><surname>Wall</surname>
<given-names>D. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2201</fpage>
<lpage>2205</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002201">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002201">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxygen heterocycles. Part XIII. From 3-arylisocoumarins to 3-arylisoquinolines and 4-aryl-5&lt;i&gt;H&lt;/i&gt;-2,3-benzodiazepines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002205</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rose</surname>
<given-names>Alain</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2205</fpage>
<lpage>2208</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002205">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002205">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXII. A note on substitution in 5&lt;i&gt;H&lt;/i&gt;-benzo[&lt;i&gt;b&lt;/i&gt;]carbazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002209</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hoellinger</surname>
<given-names>H.</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Mabille</surname>
<given-names>Ph.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2209</fpage>
<lpage>2210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002209">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002209">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXIV. A reinvestigation of the deamination of 2-, 4-, and 7-amino-5a-cholestane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002211</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Feher</surname>
<given-names>J. G.</given-names></name>
<name><surname>Hall</surname>
<given-names>R. M.</given-names></name>
<name><surname>Lack</surname>
<given-names>R. E.</given-names></name>
<name><surname>Tarasoff Jun. </surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2211</fpage>
<lpage>2215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aliphatic Friedel-Crafts reactions. Part VI. Preparation of βγ-unsaturated ketones by the acetylation of substituted cyclohexenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002215</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Groves</surname>
<given-names>J. K.</given-names></name>
<name><surname>Jones</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2215</fpage>
<lpage>2217</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002215">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002215">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Radical addition reactions. Part II. The addition of ethyl cyanoacetate to conjugated olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002217</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huang</surname>
<given-names>R. L.</given-names></name>
<name><surname>Ong</surname>
<given-names>Chong-Oon</given-names></name>
<name><surname>Ong</surname>
<given-names>S. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2217</fpage>
<lpage>2221</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002217">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002217">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions involving fluoride ion. Part I. The polyfluoroalkylation of fluorinated aromatic systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002221</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Jackson</surname>
<given-names>J. A.</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2221</fpage>
<lpage>2227</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002221">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002221">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tetranortriterpenoids. Part X. Grandifolione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connolly</surname>
<given-names>J. D.</given-names></name>
<name><surname>Handa</surname>
<given-names>K. L.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2227</fpage>
<lpage>2230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tetranortriterpenoids and related substances. Part XI. Odoratol and its congeners from &lt;i&gt;Cedrela glaziovii&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Connolly</surname>
<given-names>J. D.</given-names></name>
<name><surname>Handa</surname>
<given-names>K. L.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2230</fpage>
<lpage>2234</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenolic oxidative coupling of a 1-phenylpropylisoquinoline derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002234</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Satoh</surname>
<given-names>T.</given-names></name>
<name><surname>Yagi</surname>
<given-names>H.</given-names></name>
<name><surname>Iida</surname>
<given-names>H.</given-names></name>
<name><surname>Tanaka</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2234</fpage>
<lpage>2237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002234">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002234">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-closure to phenanthridines and acridines of some 2-arylaminomethylene derivatives of cyclohexanone and 1-tetralone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002237</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>G. E.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2237</fpage>
<lpage>2244</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002237">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002237">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Carbazole derivatives in a Kuwait mineral oil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002244</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2244</fpage>
<lpage>2247</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002244">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002244">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dehydro-L-ascorbic acid arylosazones. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002247</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Ashry</surname>
<given-names>S. H. El</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2247</fpage>
<lpage>2248</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002247">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002247">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dehydro-L-ascorbic acid arylosazones. Part II. Conversion into substituted azo-pyrazolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002248</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Ashry</surname>
<given-names>S. H. El</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2248</fpage>
<lpage>2250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002248">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002248">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dehydro-L-ascorbic acid arylosazones. Part III. Oxidation of dehydro-L-ascorbic acid arylosazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002251</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Ashry</surname>
<given-names>S. H. El</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2251</fpage>
<lpage>2253</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002251">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002251">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aza-steroids. Part VI. Approaches based on furfuraldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002253</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Popp</surname>
<given-names>Frank D.</given-names></name>
<name><surname>Schleigh</surname>
<given-names>William R.</given-names></name>
<name><surname>Katz</surname>
<given-names>Lawrence E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2253</fpage>
<lpage>2257</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002253">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002253">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dienyl complexes of transition metals. Part I. The addition of hydride to methyl-substituted arenecyclopentadienyliron cations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002257</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khand</surname>
<given-names>I. U.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Watts</surname>
<given-names>W. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2257</fpage>
<lpage>2260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002257">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002257">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dienyl complexes of transition metals. Part II. The addition of hydride to halogen-substituted arenecyclopentadienyliron cations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khand</surname>
<given-names>I. U.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Watts</surname>
<given-names>W. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2261</fpage>
<lpage>2265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry of the Leuckart reaction with 2-phenoxycyclohexanone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coe</surname>
<given-names>P. F.</given-names></name>
<name><surname>Uff</surname>
<given-names>B. C.</given-names></name>
<name><surname>Lewis</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2265</fpage>
<lpage>2268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Urinary steroids. Part VII. The Zimmermann reaction of oxo-steroids and related compounds: a correlation of structure and stereochemistry with reactivity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirk</surname>
<given-names>D. N.</given-names></name>
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Mudd</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2269</fpage>
<lpage>2275</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Insertion reactions of trifluoromethylcarbene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002276</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2276</fpage>
<lpage>2278</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002276">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002276">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ebenaceae extractives. Part III. Binaphthaquinones from Diospyros species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002279</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fallas</surname>
<given-names>A. L.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2279</fpage>
<lpage>2282</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002279">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002279">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIV. The synthesis of 18-hydroxyoestrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002283</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>J. E.</given-names></name>
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Dainis</surname>
<given-names>I.</given-names></name>
<name><surname>Pereira</surname>
<given-names>J. L. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2283</fpage>
<lpage>2289</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002283">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002283">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XXXVI. The action of acid and alkali on pteridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002289</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Yamamoto</surname>
<given-names>Hiroshi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2289</fpage>
<lpage>2292</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002289">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002289">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XXXVII. Covalent hydration in 4,6,7-trimethyl- and 2,4,6,7-tetramethyl-pteridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002292</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Yamamoto</surname>
<given-names>Hiroshi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2292</fpage>
<lpage>2294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002292">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002292">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. Mechanism of the reaction of thiophenols with nuclear-substituted β-morpholinopropiophenones and with some related quaternary iodides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002295</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Angeloni</surname>
<given-names>A. S.</given-names></name>
<name><surname>Angiolini</surname>
<given-names>L.</given-names></name>
<name><surname>Maria</surname>
<given-names>P. De</given-names></name>
<name><surname>Fini</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2295</fpage>
<lpage>2297</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002295">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002295">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Electronic effects in the acylating agent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002298</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Murdoch</surname>
<given-names>H. D.</given-names></name>
<name><surname>Nonhebel</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2298</fpage>
<lpage>2301</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 benzo-4-pyrones with dimethylsulphoxonium methylide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caplin</surname>
<given-names>G. A.</given-names></name>
<name><surname>Ollis</surname>
<given-names>W. D.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>I. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2302</fpage>
<lpage>2310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Formation and reactions of some azepines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ashby</surname>
<given-names>J.</given-names></name>
<name><surname>Cort</surname>
<given-names>L. A.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Eisner</surname>
<given-names>Ulli</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2311</fpage>
<lpage>2317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 arenediazonium hexafluoro-antimonates and -arsenates in the preparation of aryl fluorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sellers</surname>
<given-names>C.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2317</fpage>
<lpage>2319</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part II. Reaction of αβ-unsaturated acid chlorides with dienamines. Preparation of cyclohexeno(2′,1′:6,7)bicyclo[3,3,1]-non-6-ene-2,9-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002320</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Firrell</surname>
<given-names>N. F.</given-names></name>
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2320</fpage>
<lpage>2323</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002320">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002320">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Preparation and reactivity of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-3-allylcyclohexanol derivatives:— a potential π-route to the 3-bicyclo[3,3,1]nonyl cation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Macrosson</surname>
<given-names>W. D. K.</given-names></name>
<name><surname>Martin</surname>
<given-names>J.</given-names></name>
<name><surname>Parker</surname>
<given-names>W.</given-names></name>
<name><surname>Penrose</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2323</fpage>
<lpage>2328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 in the dehydrogenation of 3,3′,4,4′-tetrahydro-1,1′-binaphthyl. Some hydrogenated 1,1′-binaphthyls and benzo[&lt;i&gt;j&lt;/i&gt;]fluoranthenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002328</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>Malcolm</given-names></name>
<name><surname>Supanekar</surname>
<given-names>V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2328</fpage>
<lpage>2332</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002328">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002328">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Oxidation of phenyl- and &lt;i&gt;o&lt;/i&gt;-biphenylyl-substituted acetic and propionic acids, and of &lt;i&gt;o&lt;/i&gt;-biphenylylmethylmalonic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002332</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2332</fpage>
<lpage>2336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The oxidation of &lt;i&gt;o&lt;/i&gt;-benzoyl- and &lt;i&gt;o&lt;/i&gt;-benzyl-benzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002337</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2337</fpage>
<lpage>2338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. Synthesis of &lt;i&gt;N&lt;/i&gt;-(trimethylsilylalkyl) diamines and &lt;i&gt;N&lt;/i&gt;-(trimethylsilylalkyl)-&lt;i&gt;N&lt;/i&gt;′-(2-mercaptoethyl) diamines.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thames</surname>
<given-names>Shelby F.</given-names></name>
<name><surname>Edwards</surname>
<given-names>Laroy H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2339</fpage>
<lpage>2342</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Friedelin and related compounds. Part IX. Pachysandiol-A and isomeric friedelane-2,3-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002342</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Samson</surname>
<given-names>Antonio S.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>S. J.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>Robert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2342</fpage>
<lpage>2346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002342">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002342">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VII. The preparation of 3β,14β-dihydroxy-androst-5-en-17-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
<name><surname>Kelly</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2346</fpage>
<lpage>2349</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. (+)-Hibaene, [(+)-stachene], erythroxylol A (monogynol), erythroxylol B, and erythroxydiol A</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002349</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Martin</surname>
<given-names>A.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2349</fpage>
<lpage>2354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002349">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002349">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 novel eliminations of neutral fragments from ions in mass spectrometry. Part IV. Loss of carbon dioxide from cyclic imides and isoimides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002354</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2354</fpage>
<lpage>2358</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002354">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002354">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. The acylation of 2-amino-4-hydroxypyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002358</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Snell</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2358</fpage>
<lpage>2367</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002358">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002358">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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. The photo-Fries rearrangement of 2-dialkylamino-4-pyrimidinyl esters of alkyl and arylsulphonic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002367</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Snell</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2367</fpage>
<lpage>2370</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002367">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002367">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereoselectivity in the oxidation of thioethers to sulphoxides in the presence of &lt;i&gt;Aspergillus niger&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Auret</surname>
<given-names>B. J.</given-names></name>
<name><surname>Boyd</surname>
<given-names>D. R.</given-names></name>
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Ross</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2371</fpage>
<lpage>2374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereoselectivity in the oxidation of sulphoxides to sulphones in the presence of &lt;i&gt;Aspergillus niger&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002374</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Auret</surname>
<given-names>B. J.</given-names></name>
<name><surname>Boyd</surname>
<given-names>D. R.</given-names></name>
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2374</fpage>
<lpage>2376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002374">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002374">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isoprenoid ketones from lipid extracts of tubercle bacilli</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002376</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coles</surname>
<given-names>Lydia</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2376</fpage>
<lpage>2380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002376">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002376">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 oxides, alkoxides, and peroxides. Part I. The addition of organotin alkyl peroxides to alkyl isocyanates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bloodworth</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2380</fpage>
<lpage>2385</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 propylure, sex attractant of the pink bollworm moth</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pattenden</surname>
<given-names>Gerald</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2385</fpage>
<lpage>2388</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 V. The formation of cyclic glycols in the reduction of aromatic diketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002388</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gourley</surname>
<given-names>R. N.</given-names></name>
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2388</fpage>
<lpage>2393</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002388">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002388">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. Reactions of polyfluoroaryl-lithiums with dimethyl carbonate. Octafluorofluoren-9-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002394</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Spring</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2394</fpage>
<lpage>2397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002394">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002394">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 cyclisation of polyolefins. Part IV. The cyclisation of β-monocyclofarnesic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kitahara</surname>
<given-names>Yoshio</given-names></name>
<name><surname>Kato</surname>
<given-names>Tadahiro</given-names></name>
<name><surname>Kanno</surname>
<given-names>Susumu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2397</fpage>
<lpage>2399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. The oxidation of monoacylhydrazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002399</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aylward</surname>
<given-names>J. B.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2399</fpage>
<lpage>2402</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002399">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002399">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lead as a reducing agent in the preparation of bibenzyls and aromatic azoxy-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002403</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Azoo</surname>
<given-names>J. A.</given-names></name>
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2403</fpage>
<lpage>2405</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002403">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002403">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2,4-Trimethylanthracene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
<name><surname>Perry</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2405</fpage>
<lpage>2405</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Protonation, quaternisation, and stereochemistry of 2,2′-biphenylylene-bisdimethylamine. The thermal decomposition of related salts and the mechanism of cyclisation of 2,2′-diaminobiphenyl to carbazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002406</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2406</fpage>
<lpage>2408</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002406">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002406">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metals in the synthesis of macrocycles. Part II. The structure of the macrocycles obtained from the interaction of 1,3,3-trichloroisoindolenine and 2,4-diamino-6-phenyltriazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002409</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bamfield</surname>
<given-names>P.</given-names></name>
<name><surname>Wilkinson</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2409</fpage>
<lpage>2410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002409">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002409">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 heptulose phenylosazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Khadem</surname>
<given-names>H. El</given-names></name>
<name><surname>Rahman</surname>
<given-names>M. M. A. Abdel</given-names></name>
<name><surname>Sallam</surname>
<given-names>M. A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2411</fpage>
<lpage>2414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XX. Synthesis of some di- and tetra-methoxy-polymethylbiphenylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002414</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawson</surname>
<given-names>D. W.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>West</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2414</fpage>
<lpage>2420</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002414">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002414">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXI. Synthesis and reactions of mono- and polyethylbiphenylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002420</article-id><contrib-group><contrib contrib-type="author">
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2420</fpage>
<lpage>2422</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The synthesis and reactions of 2,3-dihydro-1,4-oxazine 4-oxide, a heterocyclic nitrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002423</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elsworth</surname>
<given-names>J. F.</given-names></name>
<name><surname>Lamchen</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2423</fpage>
<lpage>2427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002423">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002423">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 2,2-dimethyl-2,3-dihydrophenalene-1,3-dione: addition and ring-opening reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>D.</given-names></name>
<name><surname>Hankinson</surname>
<given-names>B.</given-names></name>
<name><surname>Millar</surname>
<given-names>Ian T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2428</fpage>
<lpage>2430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New intermediates and dyes. Part XI. Novel nucleophilic substitution and group elimination in the 2-carbamoylanthraquinone series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hargreaves</surname>
<given-names>T.</given-names></name>
<name><surname>Eyles</surname>
<given-names>H. G.</given-names></name>
<name><surname>Peters</surname>
<given-names>A. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2431</fpage>
<lpage>2435</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tetrahydrodibenzo-&lt;i&gt;p&lt;/i&gt;-dioxins from ethyl 1,4-benzodioxan-2-carboxylate and ethyl acetoacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002436</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2436</fpage>
<lpage>2437</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002436">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002436">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. Biogenesis of the anthraquinones in &lt;i&gt;Rubia tinctorum&lt;/i&gt; L. (madder)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002437</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2437</fpage>
<lpage>2441</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002437">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002437">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 2-bromolumisantonin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002441</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Saunderson)</surname>
<given-names>C. P. Huber (née</given-names></name>
<name><surname>Watson</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2441</fpage>
<lpage>2447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002441">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002441">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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: a novel Wittig reagent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002448</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2448</fpage>
<lpage>2452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002448">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002448">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Friedel-Crafts acylation of aromatic halogen derivatives. Part IV. The benzoylation of &lt;i&gt;o&lt;/i&gt;-, &lt;i&gt;m&lt;/i&gt;- and &lt;i&gt;p&lt;/i&gt;-dichlorobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodman</surname>
<given-names>P. A.</given-names></name>
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2452</fpage>
<lpage>2454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVII. An antifungal acetylenic furanoid keto-ester (wyerone) from shoots of the broad bean (&lt;i&gt;Vicia faba&lt;/i&gt; L.; Fam. Papilionaceae)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002455</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fawcett</surname>
<given-names>C. H.</given-names></name>
<name><surname>Spencer</surname>
<given-names>D. M.</given-names></name>
<name><surname>Wain</surname>
<given-names>R. L.</given-names></name>
<name><surname>Fallis</surname>
<given-names>A. G.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Quan</surname>
<given-names>M. Le</given-names></name>
<name><surname>Page</surname>
<given-names>C. B.</given-names></name>
<name><surname>Thaller</surname>
<given-names>V.</given-names></name>
<name><surname>Shubrook</surname>
<given-names>D. C.</given-names></name>
<name><surname>Whitham</surname>
<given-names>Miss P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2455</fpage>
<lpage>2462</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002455">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002455">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acetylenic fatty acids of &lt;i&gt;Pyrularia pubera&lt;/i&gt; seed oil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002462</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hopkins</surname>
<given-names>C. Y.</given-names></name>
<name><surname>Jevans</surname>
<given-names>A. W.</given-names></name>
<name><surname>Chisholm</surname>
<given-names>Mary J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2462</fpage>
<lpage>2465</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002462">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002462">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The absolute configuration of αα′-diphenylsuccinic acid. The (±)-and &lt;i&gt;meso&lt;/i&gt;-αα′-diphenylsuccinic anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002465</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buchan</surname>
<given-names>R.</given-names></name>
<name><surname>Watson</surname>
<given-names>M. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2465</fpage>
<lpage>2467</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002465">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002465">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ipecacuanha alkaloids. Part VIII. Chemical correlation of the indole and Ipecacuanha alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002467</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Breuer</surname>
<given-names>S. W.</given-names></name>
<name><surname>Garratt</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2467</fpage>
<lpage>2471</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002467">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002467">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reductive formylation of some quinoxaline derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002471</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>I.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2471</fpage>
<lpage>2474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002471">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002471">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. Solvent shifts induced by trifluoroacetic acid in methoxybenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002475</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>Robert G.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2475</fpage>
<lpage>2476</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. Solvent shifts of methoxy-group resonances induced by trifluoroacetic acid as an aid to structure elucidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002477</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>Robert G.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2477</fpage>
<lpage>2479</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002477">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002477">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 fatty acids with hydroxy-radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002480</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Purdy</surname>
<given-names>S. Jean</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2480</fpage>
<lpage>2481</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002480">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002480">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. Further observations in the dibenz[&lt;i&gt;b,d&lt;/i&gt;]azepin-7-one field</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002481</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peaston</surname>
<given-names>W. C.</given-names></name>
<name><surname>Proctor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2481</fpage>
<lpage>2484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002481">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002481">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;Cedrela odorata&lt;/i&gt; L. Part II. The structures of the &lt;i&gt;Cedrela&lt;/i&gt; tetracyclic triterpenes, odoratol, iso-odoratol, and odoratonen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002485</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Holder</surname>
<given-names>N. L.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Snatzke</surname>
<given-names>G.</given-names></name>
<name><surname>Fehlhaber</surname>
<given-names>H.-W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2485</fpage>
<lpage>2489</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002485">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002485">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6a-Thiathiophthens and related compounds. Part I. Synthesis of 2-methylthio-6a-thiathiophthens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002490</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beer</surname>
<given-names>R. J. S.</given-names></name>
<name><surname>Carr</surname>
<given-names>R. P.</given-names></name>
<name><surname>Cartwright</surname>
<given-names>D.</given-names></name>
<name><surname>Harris</surname>
<given-names>D.</given-names></name>
<name><surname>Slater</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2490</fpage>
<lpage>2494</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002490">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002490">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 rearrangement of α-hydroxy-ketones to lactones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002494</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Gandhi</surname>
<given-names>R. P.</given-names></name>
<name><surname>Southam</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2494</fpage>
<lpage>2500</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002494">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002494">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Baeyer-Villiger oxidation of alkyl oxocyclohexanecarboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002500</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hubert</surname>
<given-names>A. J.</given-names></name>
<name><surname>Starcher</surname>
<given-names>P. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2500</fpage>
<lpage>2502</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002500">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002500">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Friedel–Crafts acylations of aromatic hydrocarbons. Part VII. The acetylation and benzoylation of 2,3-dimethylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002502</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Thadani</surname>
<given-names>C. K.</given-names></name>
<name><surname>Thorburn</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2502</fpage>
<lpage>2508</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002502">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002502">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ether cleavage of 7-oxabicyclo[2,2,1]heptane derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002508</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kitahara</surname>
<given-names>Yoshio</given-names></name>
<name><surname>Kato</surname>
<given-names>Tadahiro</given-names></name>
<name><surname>Ototani</surname>
<given-names>Noboru</given-names></name>
<name><surname>Inoue</surname>
<given-names>Akira</given-names></name>
<name><surname>Izumi</surname>
<given-names>Hideo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2508</fpage>
<lpage>2510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002508">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002508">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acetylenic esters. Part III. Reactions of thiocarbonyl compounds with methyl propiolate, methyl methylpropiolate, and methyl phenylpropiolate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002510</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dallas</surname>
<given-names>G.</given-names></name>
<name><surname>Lown</surname>
<given-names>J. W.</given-names></name>
<name><surname>Ma</surname>
<given-names>J. C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2510</fpage>
<lpage>2514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002510">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002510">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 10-hydroperoxy-9-anthrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bedford</surname>
<given-names>C. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2514</fpage>
<lpage>2515</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Auto-oxidation of lanost-8-en-3β-yl acetate: ring D derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002516</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scotney</surname>
<given-names>J.</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2516</fpage>
<lpage>2519</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002516">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002516">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of the Scholl reaction: oxidative dehydrogenation involving 1-ethoxynaphthalene and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002519</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2519</fpage>
<lpage>2526</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The self-condensation of 3,4-dimethylpyrrole: an alternative reaction pathway</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002526</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bender</surname>
<given-names>C. O.</given-names></name>
<name><surname>Bonnett</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2526</fpage>
<lpage>2528</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002526">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002526">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. Two norditerpenoid tertiary alcohols and three diterpenoid epoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>A.</given-names></name>
<name><surname>Murray</surname>
<given-names>R. D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2529</fpage>
<lpage>2533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies related to penicillins. Part I. 6-α-Chloropenicillanic acid and its reaction with nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002533</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McMillan</surname>
<given-names>I.</given-names></name>
<name><surname>Stoodley</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2533</fpage>
<lpage>2537</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002533">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002533">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. The reaction of trimethylsilane with trifluoronitrosomethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002537</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Delany</surname>
<given-names>A. C.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2537</fpage>
<lpage>2539</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002537">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002537">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 eliminations of neutral fragments from ions during mass spectrometry. Part V. Evidence for cyclisation processes in the elimination of methyl from stilbene analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Ward</surname>
<given-names>S. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2540</fpage>
<lpage>2543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of heterocyclic compounds. Part V. A synthesis of thiothiophthenes and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002543</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dingwall</surname>
<given-names>J. G.</given-names></name>
<name><surname>McKenzie</surname>
<given-names>S.</given-names></name>
<name><surname>Reid</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2543</fpage>
<lpage>2548</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002543">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002543">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The elimination of carbon monoxide from acid derivatives. Part III. Planar carbonium ions as necessary intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002548</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pratt</surname>
<given-names>David G.</given-names></name>
<name><surname>Rothstein</surname>
<given-names>Eugene</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2548</fpage>
<lpage>2554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002548">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002548">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pectic substances from lucerne (&lt;i&gt;Medicago sativa&lt;/i&gt;). Part II. Acidic oligosaccharides from partial hydrolysis of leaf and stem pectic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Gestetner</surname>
<given-names>B.</given-names></name>
<name><surname>Molloy</surname>
<given-names>J. A.</given-names></name>
<name><surname>Uddin</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2554</fpage>
<lpage>2559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mycological chemistry. Part XXIII. The structure of flavomannin, a metabolite of &lt;i&gt;Penicillium wortmanni&lt;/i&gt; Klöck</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002560</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atherton</surname>
<given-names>John</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>
<name><surname>Roffey</surname>
<given-names>Partick</given-names></name>
<name><surname>Wilcox</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2560</fpage>
<lpage>2564</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. The synthesis of &lt;i&gt;p&lt;/i&gt;-di-(2-chloroethyl)aminophenyl-L-alanine (melphalan) labelled with tritium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002564</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wade</surname>
<given-names>Roy</given-names></name>
<name><surname>Murthy</surname>
<given-names>T. Srinivasa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2564</fpage>
<lpage>2567</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002564">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002564">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Syntheses of steroidal 1,4,6-trien-3-ones.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002568</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Turner</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2568</fpage>
<lpage>2570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002568">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002568">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton magnetic resonance spectra of &lt;i&gt;N&lt;/i&gt;-substituted 3-aminocrotonic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002570</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sánchez</surname>
<given-names>A. Gómez</given-names></name>
<name><surname>Aldave</surname>
<given-names>M. Tena</given-names></name>
<name><surname>Scheidegger</surname>
<given-names>U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2570</fpage>
<lpage>2573</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002570">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002570">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LV. Androstane-17β-carboxylic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002574</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Renwick</surname>
<given-names>J. D.</given-names></name>
<name><surname>Scopes</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2574</fpage>
<lpage>2576</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002574">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002574">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 alkali on some 9-substituted adenines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mian</surname>
<given-names>A. M.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2577</fpage>
<lpage>2579</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. The isolation of buchanaxanthone and two related xanthones from &lt;i&gt;Garcinia buchananii&lt;/i&gt; Baker</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002579</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>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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2579</fpage>
<lpage>2583</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. Syntheses of model compounds related to xanthatin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002583</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhanot</surname>
<given-names>Opinder Singh</given-names></name>
<name><surname>Dutta</surname>
<given-names>Phanindra Chandra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2583</fpage>
<lpage>2588</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002583">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002583">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 on terpenoids. Part XIV. Synthesis of a hydroazulene derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002589</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhanot</surname>
<given-names>Opinder Singh</given-names></name>
<name><surname>Dutta</surname>
<given-names>Phanindra Chandra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2589</fpage>
<lpage>2590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002589">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002589">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Evidence for the formation of a hexahydrotriazine in the condensation of acetaldehyde with methylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002591</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carter</surname>
<given-names>G. B.</given-names></name>
<name><surname>McIvor</surname>
<given-names>M. C.</given-names></name>
<name><surname>Miller</surname>
<given-names>R. G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2591</fpage>
<lpage>2592</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002591">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002591">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyhalogenoallenes. Part V. Perfluoropenta-1,2-diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Braithwaite</surname>
<given-names>A.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2593</fpage>
<lpage>2598</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part III. Reaction of αβ-unsaturated acid chlorides with enamines of acyclic ketones. Preparation of cyclohexane-1,3-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002599</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hargreaves</surname>
<given-names>J. R.</given-names></name>
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2599</fpage>
<lpage>2603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002599">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002599">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 steroids. Part I. Oxidation products of 3-methoxyoestra-1,3,5(10)-trien-17β-yl acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cambie</surname>
<given-names>R. C.</given-names></name>
<name><surname>Manning</surname>
<given-names>T. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2603</fpage>
<lpage>2608</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Some free-radical reactions of perfluoro-&lt;i&gt;N&lt;/i&gt;-fluoropiperidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002608</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>
<name><surname>Williamson</surname>
<given-names>G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2608</fpage>
<lpage>2612</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002608">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002608">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. Elimination in 2-sulphonylethyl carboxylates: a method for the protection of carboxy-groups in peptide synthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002612</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>A. W.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2612</fpage>
<lpage>2617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002612">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002612">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Long-chain acyloins and vicinal diketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002617</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>
<name><surname>Warren</surname>
<given-names>B. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2617</fpage>
<lpage>2621</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002617">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002617">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Reaction with hydrogen peroxide and acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>Russell</surname>
<given-names>E. R. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2621</fpage>
<lpage>2625</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 kamala. Isolation and structure of two new components</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002625</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Green</surname>
<given-names>C. L.</given-names></name>
<name><surname>Tuck</surname>
<given-names>B.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2625</fpage>
<lpage>2630</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002625">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002625">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIII. The reaction of trialkyltin alkoxides and of bistrialkyltin oxides with sulphur dioxide, sulphodi-imides, and sulphinylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002630</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Kennedy</surname>
<given-names>John D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2630</fpage>
<lpage>2640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002630">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002630">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XIV. The decarboxylation of trialkyltin carbamates by isocyanates and isothiocyanates: a new route to carbodi-imides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002640</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2640</fpage>
<lpage>2646</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Totally synthetic steroid hormones. Part XIX. (±)-18-Methyl-19-norpregn-4-ene-3,11,20-trione, (±)-21-acetoxy-11β,17-dihydroxy-18-methyl-19-norpregn-4-ene-3,20-dione, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002647</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gadsby</surname>
<given-names>B.</given-names></name>
<name><surname>Leeming</surname>
<given-names>M. R. G.</given-names></name>
<name><surname>Greenspan</surname>
<given-names>G.</given-names></name>
<name><surname>Smith</surname>
<given-names>Herchel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2647</fpage>
<lpage>2656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002647">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002647">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 physical properties of some 2-alkylthio-4-oxoquinoline-3-carboxylate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002656</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kay</surname>
<given-names>I. T.</given-names></name>
<name><surname>Taylor</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2656</fpage>
<lpage>2661</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002656">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002656">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Derivatives of 2-amino-2-deoxy-L-talitol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002661</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gigg</surname>
<given-names>Roy</given-names></name>
<name><surname>Warren</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2661</fpage>
<lpage>2666</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002661">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002661">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXIV. Molecular ion abundances in relation to ionisation potentials</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002666</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yeo</surname>
<given-names>Adrian N. H.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2666</fpage>
<lpage>2667</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002666">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002666">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic analogues of polynucleotides. Part IV. Carboxymethyl derivatives of uridine and of thymidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Halford</surname>
<given-names>M. H.</given-names></name>
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2667</fpage>
<lpage>2670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 (±)-bakuchiol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002671</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carnduff</surname>
<given-names>J.</given-names></name>
<name><surname>Miller</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2671</fpage>
<lpage>2673</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002671">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002671">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XI. The preparation and infrared spectra of vicinal cholestanediols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002674</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davey</surname>
<given-names>C. W.</given-names></name>
<name><surname>McGinnis</surname>
<given-names>E. L.</given-names></name>
<name><surname>Chancellor)</surname>
<given-names>(Mrs.) J. M. McKeown (née</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Pemberton</surname>
<given-names>M. W.</given-names></name>
<name><surname>Young</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2674</fpage>
<lpage>2682</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002674">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002674">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XII. Reactions of 5α-ergost-7-en-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002683</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrews</surname>
<given-names>A. T. de B.</given-names></name>
<name><surname>Pemberton</surname>
<given-names>M. W.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2683</fpage>
<lpage>2684</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002683">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002683">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;-substituted heterocyclic cations. Part VII. Products of reaction of alcohols with &lt;i&gt;N&lt;/i&gt;-cyanoquinolinium fluoroborate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002684</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2684</fpage>
<lpage>2686</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002684">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002684">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 dipterocarpaceae resins. Part II. Structure of dryobalanone from &lt;i&gt;Dryobalanops aromatica&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002686</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheung</surname>
<given-names>H. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2686</fpage>
<lpage>2689</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002686">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002686">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polyazabenzo[&lt;i&gt;a&lt;/i&gt;]pyrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002689</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grout</surname>
<given-names>R. J.</given-names></name>
<name><surname>Partridge</surname>
<given-names>M. W.</given-names></name>
<name><surname>Sprake</surname>
<given-names>J. M.</given-names></name>
<name><surname>Vipond</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2689</fpage>
<lpage>2693</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002689">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002689">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 pyrrolo[1,2-&lt;i&gt;c&lt;/i&gt;]pyrimidines from 4-methyl-6-phenylpyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002693</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>J.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2693</fpage>
<lpage>2697</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002693">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002693">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Deamination of 5α-amino- and 6α-amino-5β-hydroxy-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002698</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. G. L.</given-names></name>
<name><surname>Marples</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2698</fpage>
<lpage>2700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002698">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002698">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacement reactions in carbohydrates. Part VIII. Identification of the minor products from the reactions of 2,3-&lt;i&gt;O&lt;/i&gt;-isopropylidene-5-&lt;i&gt;O&lt;/i&gt;-methylsulphonyl-D-lyxofuranose and 2,3-&lt;i&gt;O&lt;/i&gt;-isopropylidene-5-&lt;i&gt;O&lt;/i&gt;-&lt;i&gt;p&lt;/i&gt;-tolylsulphonyl-L-rhamnofuranose with sodium methoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002701</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Hunedy</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2701</fpage>
<lpage>2703</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002701">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002701">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The anomalous Schmidt reactions of acrylic acid and its esters and acrylonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002703</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>A. J.</given-names></name>
<name><surname>Marks</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2703</fpage>
<lpage>2705</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002703">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002703">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridopyrimidines. Part IV. The preparation of pyrido[4,3-&lt;i&gt;d&lt;/i&gt;]pyrimidines from pryano[4,3-&lt;i&gt;d&lt;/i&gt;]pyrimidin-5-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002706</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2706</fpage>
<lpage>2708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002706">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002706">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of Group IV organometallic compounds. Part XI. Some insertion reactions of alkylsilyl and alkylstannyl sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002709</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Itoh</surname>
<given-names>Kenji</given-names></name>
<name><surname>Matsuzaki</surname>
<given-names>Kimishige</given-names></name>
<name><surname>Ishii</surname>
<given-names>Yoshio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2709</fpage>
<lpage>2712</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002709">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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, addition, and substitution reactions of arylsulphenate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002713</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hogg</surname>
<given-names>D. R.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. H.</given-names></name>
<name><surname>Vipond</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2713</fpage>
<lpage>2716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002713">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002713">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,2:5,6-Di-&lt;i&gt;O&lt;/i&gt;-cyclohexylidene-3-&lt;i&gt;C&lt;/i&gt;-methyl-α-D-allofuranose and other branched-chain analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rees</surname>
<given-names>R. D.</given-names></name>
<name><surname>James</surname>
<given-names>K.</given-names></name>
<name><surname>Tatchell</surname>
<given-names>A. R.</given-names></name>
<name><surname>Williams</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2716</fpage>
<lpage>2721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002716">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and nuclear magnetic resonance characterization of 1,1,2,2-tetra-aminoethanes, 1,1,2-triaminoethenes, and 1,2-dialkoxy-1,2-di-aminoethanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferruti</surname>
<given-names>Paolo</given-names></name>
<name><surname>Segre</surname>
<given-names>Annalaura</given-names></name>
<name><surname>Fere</surname>
<given-names>Angelino</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2721</fpage>
<lpage>2725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002721">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 stereoselective synthesis of substituted maleic esters by use of phosphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002725</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huff</surname>
<given-names>R. K.</given-names></name>
<name><surname>Moppett</surname>
<given-names>C. E.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2725</fpage>
<lpage>2726</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002725">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002725">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryne chemistry. Part XIII. Polychloroaromatic compounds. Part III. The generation and reactions of trichloropyridynes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002727</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>J. D.</given-names></name>
<name><surname>Wakefield</surname>
<given-names>B. J.</given-names></name>
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
<name><surname>Jablonski</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2727</fpage>
<lpage>2730</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002727">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002727">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermolytic reactions of benzotriazinone and isatoic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002730</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crabtree</surname>
<given-names>H. E.</given-names></name>
<name><surname>Smalley</surname>
<given-names>R. K.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2730</fpage>
<lpage>2733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002730">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002730">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 3-benzo[&lt;i&gt;b&lt;/i&gt;]thienyl-lithium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002733</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dickinson</surname>
<given-names>R. P.</given-names></name>
<name><surname>Iddon</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2733</fpage>
<lpage>2737</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002733">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lignans and related phenols. Part VII. Reactions of some 2-arylfurans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002737</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2737</fpage>
<lpage>2740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002737">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002737">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 I. The preparation of aromatic fluorocarbons from fluorocyclohexadienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002740</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Doyle</surname>
<given-names>A. M.</given-names></name>
<name><surname>Pedler</surname>
<given-names>A. E.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2740</fpage>
<lpage>2742</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002740">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002740">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IV. 2-Hydroxy-3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002743</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>K. M.</given-names></name>
<name><surname>Davis</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2743</fpage>
<lpage>2747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002743">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002743">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. 4-and 6-Halogeno-derivatives of &lt;i&gt;N&lt;/i&gt;-2-chloroethyl-&lt;i&gt;N&lt;/i&gt;-ethyl-3-aminomethylbenzo[&lt;i&gt;b&lt;/i&gt;]thiophen hydrochloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002747</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>Sawhney</surname>
<given-names>S. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2747</fpage>
<lpage>2751</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction between cyanide and the mixed disulphide of cysteine and penicillamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002751</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyde</surname>
<given-names>T. R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2751</fpage>
<lpage>2753</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002751">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002751">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aminosaccharides. Part III. Acid hydrolysis of 6-&lt;i&gt;O&lt;/i&gt;-(2-amino-2-deoxy-α[and β]-D-glucopyranosyl)-D-galactose hydrochloride and its &lt;i&gt;N&lt;/i&gt;-acetyl and &lt;i&gt;N&lt;/i&gt;-2,4-dinitrophenyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002753</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lloyd</surname>
<given-names>P. F.</given-names></name>
<name><surname>Evans</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2753</fpage>
<lpage>2755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002753">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002753">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Formation of pyrimidine-iones and related compounds from dicarboxylic acid amides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beckwith</surname>
<given-names>A. L. J.</given-names></name>
<name><surname>Hickman</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2756</fpage>
<lpage>2759</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 phenyl migrations in organophosphorus compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002760</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brophy</surname>
<given-names>J. J.</given-names></name>
<name><surname>Freeman</surname>
<given-names>K. L.</given-names></name>
<name><surname>Gallagher</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2760</fpage>
<lpage>2765</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002760">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002760">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The absolute configuration and the structures of chlorophyll and bacteriochlorophyll</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002765</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>Ian</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2765</fpage>
<lpage>2770</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002765">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002765">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. Competitive oxidative demethylation and debromination</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002770</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adderley</surname>
<given-names>C. J. R.</given-names></name>
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2770</fpage>
<lpage>2774</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002770">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002770">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 the genus &lt;i&gt;Datura&lt;/i&gt;, section brugmansia. Part V. Alkaloids of &lt;i&gt;D. sanguinea&lt;/i&gt; R. and P. and related esters of tropane-3α,6β,7β-triol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002775</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>W. C.</given-names></name>
<name><surname>Major</surname>
<given-names>Valerie A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2775</fpage>
<lpage>2778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002775">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002775">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acyclic imides. A general method of &lt;i&gt;N&lt;/i&gt;-acylation of amides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baburao</surname>
<given-names>K.</given-names></name>
<name><surname>Costello</surname>
<given-names>(Miss) A. M.</given-names></name>
<name><surname>Petterson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Sander</surname>
<given-names>G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2779</fpage>
<lpage>2781</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 from the Euphorbiaceae. Part I. The structure of crotonin, a norditerpene from &lt;i&gt;Croton lucidus&lt;/i&gt; L</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002781</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2781</fpage>
<lpage>2785</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002781">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002781">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 constituents of the blue-green algae &lt;i&gt;Nostoc muscorum&lt;/i&gt;, &lt;i&gt;Anacystis nidulans&lt;/i&gt;, &lt;i&gt;Phormidium luridium&lt;/i&gt; and &lt;i&gt;Chlorogloea fritschii&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002785</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Han</surname>
<given-names>Jerry</given-names></name>
<name><surname>McCarthy</surname>
<given-names>E. D.</given-names></name>
<name><surname>Calvin</surname>
<given-names>Melvin</given-names></name>
<name><surname>Benn</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2785</fpage>
<lpage>2791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002785">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002785">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 lophocerine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002791</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Donovan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Horan</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2791</fpage>
<lpage>2795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002791">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002791">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VI. 2-Phosphoniaethanesulphonate betaines. The sulphonation of vinyl phosphonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002795</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2795</fpage>
<lpage>2801</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002795">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002795">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological oxidation of long-chain aliphatic compounds. Part I. Alkanes and alk-1-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002801</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. F.</given-names></name>
<name><surname>Howe</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2801</fpage>
<lpage>2808</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002801">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002801">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological oxidation of long-chain aliphatic compounds. Part II. Branched-chain alkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002809</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2809</fpage>
<lpage>2815</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002809">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002809">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological oxidation of long-chain aliphatic compounds. Part III. 1-Halogenoalkanes, 1-cyanohexadecane, and 1-alkoxyalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002816</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. F.</given-names></name>
<name><surname>Howe</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2816</fpage>
<lpage>2821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002816">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002816">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological oxidation of long-chain aliphatic compounds. Part IV. Alkane derivatives having polar terminal groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002821</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>D. F.</given-names></name>
<name><surname>Howe</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2821</fpage>
<lpage>2827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002821">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002821">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological oxidation of long-chain aliphatic compounds. Part V. Mechanism of hydroxylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002827</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2827</fpage>
<lpage>2833</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002827">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002827">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and alkylation reactions. Part IV. The cyclisation of alkyl-substituted phenoxyacetyl chlorides to benzofuran-3(2&lt;i&gt;H&lt;/i&gt;)-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>Scollick</surname>
<given-names>N. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2833</fpage>
<lpage>2836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 and alkylation reactions. Part V. Some syntheses of tricyclic derivatives of benzo[&lt;i&gt;b&lt;/i&gt;]furan-3(2&lt;i&gt;H&lt;/i&gt;)-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>Scollick</surname>
<given-names>N. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2836</fpage>
<lpage>2841</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXXVIII. The conversion of hydroxysteroids (R&lt;sup&gt;1&lt;/sup&gt;OH) into &lt;i&gt;O&lt;/i&gt;-substituted glycollic esters (R&lt;sup&gt;1&lt;/sup&gt;O·CH&lt;sub&gt;2&lt;/sub&gt;·CO&lt;sub&gt;2&lt;/sub&gt;R&lt;sup&gt;2&lt;/sup&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002841</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>J. M.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Morisawa</surname>
<given-names>Y.</given-names></name>
<name><surname>Woodgate</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2841</fpage>
<lpage>2844</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002841">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002841">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polychloroaromatic compounds. Part IV. Oxidation of 2- and 4-&lt;i&gt;N&lt;/i&gt;-alkylaminotetrachloropyridines and nucleophilic substitution of tetrachloronitropyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002844</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roberts</surname>
<given-names>S. M.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2844</fpage>
<lpage>2848</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002844">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002844">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preparation and rearrangement of bromo- and iodo-pyrrolo[1,2-&lt;i&gt;a&lt;/i&gt;]-quinoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002848</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Roy</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2848</fpage>
<lpage>2852</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002848">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002848">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 parasorbic acid (hex-2-en-5-olide) by the rowan berry (&lt;i&gt;Sorbus aucuparia&lt;/i&gt; L.)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002852</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Firth</surname>
<given-names>Patricia A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2852</fpage>
<lpage>2856</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002852">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002852">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical properties and tautomeric behaviour of 1,4-dihydroxypyridazino[4,5-&lt;i&gt;d&lt;/i&gt;]pyridazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002857</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adembri</surname>
<given-names>G.</given-names></name>
<name><surname>Sio</surname>
<given-names>F. De</given-names></name>
<name><surname>Nesi</surname>
<given-names>R.</given-names></name>
<name><surname>Scotton</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2857</fpage>
<lpage>2861</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002857">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002857">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 [1,5]-benzodiazocines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002862</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Auret</surname>
<given-names>B. J.</given-names></name>
<name><surname>Grundon</surname>
<given-names>M. F.</given-names></name>
<name><surname>McMaster</surname>
<given-names>I. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2862</fpage>
<lpage>2863</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002862">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002862">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions with amines of disulphides derived from thiazolium salts. Part I. Primary and secondary amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002864</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2864</fpage>
<lpage>2871</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002864">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002864">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions with amines of disulphides derived from thiazolium salts. Part II. Tertiary and aromatic amines and the thiolation reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002871</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2871</fpage>
<lpage>2876</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002871">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002871">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformation and rearrangement reactions of derivatives of 10,11-dihydrodibenzoxepin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002877</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Shibuya</surname>
<given-names>S.</given-names></name>
<name><surname>Ollis</surname>
<given-names>W. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2877</fpage>
<lpage>2883</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002877">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002877">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2-pyridyl polyamines. Synthesis, spectra, and proton dissociation constants</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002884</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Romary</surname>
<given-names>J. Kirk</given-names></name>
<name><surname>Zachariasen</surname>
<given-names>Rita D.</given-names></name>
<name><surname>Barger</surname>
<given-names>J. D.</given-names></name>
<name><surname>Schiesser</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2884</fpage>
<lpage>2887</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002884">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002884">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Zinc reductions of keto-groups to methylene groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002887</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yamamura</surname>
<given-names>Shosuke</given-names></name>
<name><surname>Hirata</surname>
<given-names>Yoshimasa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2887</fpage>
<lpage>2889</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002887">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002887">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 method for the carbonylation of allylic halides with insertion of acetylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chiusoli</surname>
<given-names>G. P.</given-names></name>
<name><surname>Dubini</surname>
<given-names>M.</given-names></name>
<name><surname>Ferraris</surname>
<given-names>M.</given-names></name>
<name><surname>Guerrieri</surname>
<given-names>F.</given-names></name>
<name><surname>Merzoni</surname>
<given-names>S.</given-names></name>
<name><surname>Mondelli</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2889</fpage>
<lpage>2890</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies related to penicillins. Part II. The rearrangement of 6-β-aminopenicillanic acid to 2,3-dihydro-6-methoxycarbonyl-2,2-di-methyl-1,4-thiazin-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002891</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stoodley</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2891</fpage>
<lpage>2894</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002891">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002891">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVII. Elimination pathways in derivatives of β-sulphonylsulphonic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>E. J.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2895</fpage>
<lpage>2898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aliphatic Friedel-Crafts reactions. Part VII. Preparation of αβ- and βγ-unsaturated ketones from substituted cyclohexenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002898</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Groves</surname>
<given-names>J. K.</given-names></name>
<name><surname>Jones</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2898</fpage>
<lpage>2900</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002898">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002898">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 II. Rearrangement of some &lt;i&gt;N&lt;/i&gt;-aroyldiphenylamines and the intermolecular character of the reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002900</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2900</fpage>
<lpage>2904</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002900">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002900">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 amides derived from heterocyclic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002904</article-id><contrib-group><contrib contrib-type="author">
<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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2904</fpage>
<lpage>2908</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002904">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002904">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Skeletal rearrangement of α-hydroxy-ketones upon electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002909</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Frearson</surname>
<given-names>M. J.</given-names></name>
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2909</fpage>
<lpage>2912</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002909">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002909">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. The preparation of 3β,18-dihydroxy-androst-5-en-17-one and its conversion into 3β-hydroxy-18-nor-13α-androst-5-en-17-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002913</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
<name><surname>Kelly</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2913</fpage>
<lpage>2915</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002913">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002913">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. A new route to 19-nor-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002915</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laing</surname>
<given-names>S. B.</given-names></name>
<name><surname>Sykes</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2915</fpage>
<lpage>2918</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002915">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002915">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part IV. Reaction of αβ-unsaturated acid chlorides with enamines of aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002918</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2918</fpage>
<lpage>2924</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002918">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002918">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 γδ-unsaturated ketones with peracids. 2,7-Dioxabicyclo-[2,2,1]heptanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gaoni</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2925</fpage>
<lpage>2934</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2,7-dioxabicyclo[2,2,1]heptanes with &lt;i&gt;m&lt;/i&gt;-chloroperbenzoic acid. 2,7,8-Trioxabicyclo[3,2,1]octanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002934</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gaoni</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2934</fpage>
<lpage>2941</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002934">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002934">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Optical rotatory dispersion and circular dichroism studies: bicyclic sesquiterpene ketones of the eudesmane series and related thioacetals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002941</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Humber</surname>
<given-names>D. C.</given-names></name>
<name><surname>Pinder</surname>
<given-names>A. R.</given-names></name>
<name><surname>Wallis</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2941</fpage>
<lpage>2947</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The total synthesis of (±)-lycoramine. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002947</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hazama</surname>
<given-names>Naohiko</given-names></name>
<name><surname>Irie</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Mizutani</surname>
<given-names>Tamio</given-names></name>
<name><surname>Shingu</surname>
<given-names>Tetsuro</given-names></name>
<name><surname>Takada</surname>
<given-names>Masao</given-names></name>
<name><surname>Uyeo</surname>
<given-names>Shojiro</given-names></name>
<name><surname>Yoshitake</surname>
<given-names>Akira</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2947</fpage>
<lpage>2953</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002947">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002947">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The total synthesis of (±)-lycoramine. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002954</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Misaka</surname>
<given-names>Yoshiharu</given-names></name>
<name><surname>Mizutani</surname>
<given-names>Tamio</given-names></name>
<name><surname>Sekido</surname>
<given-names>Mamoru</given-names></name>
<name><surname>Uyeo</surname>
<given-names>Shojiro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2954</fpage>
<lpage>2959</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002954">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002954">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pseudoazulenes. Part VI. Indenopyrazoles and the attempted preparation of an indenoisoxazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002959</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Hewson</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2959</fpage>
<lpage>2964</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002959">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002959">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Potassium ferricyanide oxidation of &lt;i&gt;N&lt;/i&gt;-methyltryptamine in liquid ammonia</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002965</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Suzuki</surname>
<given-names>T.</given-names></name>
<name><surname>Ogasawara</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2965</fpage>
<lpage>2968</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002965">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002965">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 VIII. The blueing of &lt;i&gt;Boletus&lt;/i&gt; species. Variegatic acid, a hydroxytetronic acid from &lt;i&gt;Boletus&lt;/i&gt; species and a reassessment of the structure of boletol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002968</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaumont</surname>
<given-names>P. C.</given-names></name>
<name><surname>Edwards</surname>
<given-names>R. L.</given-names></name>
<name><surname>Elsworthy</surname>
<given-names>G. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2968</fpage>
<lpage>2974</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002968">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002968">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azasteroids. Part III. The synthesis of 8-aza-19-norprogesterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002975</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowler (Mrs.) </surname>
<given-names>J.</given-names></name>
<name><surname>Clarkson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2975</fpage>
<lpage>2978</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002975">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002975">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 peroxides containing functional groups. Part I. The preparation and properties of some α-oxo-hydroperoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002978</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cubbon</surname>
<given-names>R. C. P.</given-names></name>
<name><surname>Hewlett</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2978</fpage>
<lpage>2982</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002978">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002978">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 peroxides containing functional groups. Part II. The reaction of hydrogen peroxide with β- and γ-oxo-acids and esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002983</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cubbon</surname>
<given-names>R. C. P.</given-names></name>
<name><surname>Hewlett</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2983</fpage>
<lpage>2986</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002983">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002983">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 peroxides containing functional groups. Part III. The reaction of hydrogen peroxide and t-butyl hydroperoxide with 4-oxovaleric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002986</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cubbon</surname>
<given-names>R. C. P.</given-names></name>
<name><surname>Hewlett</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2986</fpage>
<lpage>2988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002986">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002986">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XV. Formation and nucleophilic substitution of polyfluoropyridazinium cations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002989</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>MacBride</surname>
<given-names>J. A. H.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2989</fpage>
<lpage>2994</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002989">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002989">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pectic substances from lucerne (&lt;i&gt;Medicago sativa&lt;/i&gt;). Part III. Fractionation of polysaccharides extracted with water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002994</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Molloy</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2994</fpage>
<lpage>2999</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002994">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002994">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXI. Some reactions of the allylic group in the plant cell-division promoting factor, zeatin, and its nucleoside and nucleotide derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680002999</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
<name><surname>Smallwood</surname>
<given-names>B. M.</given-names></name>
<name><surname>Wilson</surname>
<given-names>D. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>2999</fpage>
<lpage>3004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680002999">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680002999">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclisation of humulene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greenwood</surname>
<given-names>J. M.</given-names></name>
<name><surname>Solomon</surname>
<given-names>M. D.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>J. K.</given-names></name>
<name><surname>Torre</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3004</fpage>
<lpage>3008</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-(L-lysyl-L-alanylglycine) hydrobromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003008</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3008</fpage>
<lpage>3011</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 potential insecticides. Part I. 2,2-Dichlorovinyl carbamates and carbonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kay</surname>
<given-names>I. T.</given-names></name>
<name><surname>Punja</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3011</fpage>
<lpage>3014</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 III. Some steroidal ketimines and amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marples</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3015</fpage>
<lpage>3017</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Autoxidation of 2α-hydroxy-5α-cholestan-3-one in methanolic potassium hydroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003017</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lack</surname>
<given-names>Ruth E.</given-names></name>
<name><surname>Ridley</surname>
<given-names>Anne B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3017</fpage>
<lpage>3020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003017">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003017">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 free radicals to unsaturated systems. Part XV. Further investigation of the direction of radical addition to chloro-1,1-difluoroethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003020</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>R.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Tipping</surname>
<given-names>A. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3020</fpage>
<lpage>3025</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003020">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003020">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 heterocyclic phosphorus compounds. Part III. Substituted phenoxaphosphines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>I. G. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3026</fpage>
<lpage>3028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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: the origin of C-6 and C-6a</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003029</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Green</surname>
<given-names>C. L.</given-names></name>
<name><surname>Whiting</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3029</fpage>
<lpage>3032</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003029">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003029">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 IX. 5-Halogenomethyl-5-methyl- and 5,5-dimethyl-2-oxo-2-piperidino-1,3,2-dioxaphosphorinans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003033</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Mitchell</surname>
<given-names>E. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3033</fpage>
<lpage>3036</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003033">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003033">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isoindoles from 2,5-disubstituted pyrroles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bender</surname>
<given-names>C. O.</given-names></name>
<name><surname>Bonnett</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3036</fpage>
<lpage>3040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 preparation of βγ-unsaturated esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moppett</surname>
<given-names>C. E.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3040</fpage>
<lpage>3042</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lirioresinol-C dimethyl ether, a diaxially substituted 3,7-dioxabicyclo[3,3,0]octane lignan from &lt;i&gt;Macropiper excelsum&lt;/i&gt;(Forst.f.) Miq.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003042</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briggs</surname>
<given-names>Lindsay H.</given-names></name>
<name><surname>Cambie</surname>
<given-names>R. C.</given-names></name>
<name><surname>Couch</surname>
<given-names>R. A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3042</fpage>
<lpage>3045</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003042">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003042">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclo-octanes. Part II. 1,4-Disubstituted cyclo-octanes.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>C. S.</given-names></name>
<name><surname>Jonas</surname>
<given-names>D. A.</given-names></name>
<name><surname>Graham</surname>
<given-names>S. H.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3045</fpage>
<lpage>3049</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-Bis-(5-methyl-1,4-benzoquinon-2-yl)ethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003049</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hunt</surname>
<given-names>S. E.</given-names></name>
<name><surname>Lindsey</surname>
<given-names>A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3049</fpage>
<lpage>3051</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003049">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003049">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The total synthesis of (±)-ochotensine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003051</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irie</surname>
<given-names>Hiroshi</given-names></name>
<name><surname>Kishimoto</surname>
<given-names>Teiji</given-names></name>
<name><surname>Uyeo</surname>
<given-names>Shojiro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3051</fpage>
<lpage>3057</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003051">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003051">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 heterocyclic compounds. Part XXII. Routes to naphthimidazoles and imidazoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003058</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
<name><surname>Sutton</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3058</fpage>
<lpage>3062</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003058">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003058">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acyl (phosphoryl) transfer by use of &lt;i&gt;gem&lt;/i&gt;-dihalides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003062</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>V. M.</given-names></name>
<name><surname>Hutchinson</surname>
<given-names>D. W.</given-names></name>
<name><surname>Varey</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3062</fpage>
<lpage>3065</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003062">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003062">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 between ethyl-lithium and α-methylstyrene in benzene at 30°; formation of 1,3-dimethyl-3-phenyl-1-propylindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003065</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Margerison</surname>
<given-names>D.</given-names></name>
<name><surname>Nyss</surname>
<given-names>Miss V. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3065</fpage>
<lpage>3067</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003065">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003065">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXVI. The configuration of the glucoside linkage in protoaphins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
<name><surname>Craik</surname>
<given-names>J. C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3068</fpage>
<lpage>3072</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: 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 VIII. Some volatile neutral products of the oxidation of (+)-car-3-ene with permanganate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003073</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burns</surname>
<given-names>W. D. P.</given-names></name>
<name><surname>Carson</surname>
<given-names>(Miss) M. S.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3073</fpage>
<lpage>3079</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003073">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003073">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arylazo-steroids. Part IV. The reaction of phenylhydrazine and 1-methyl-1-phenylhydrazine with bromo- and dibromo-5α-cholestanones; osazone formation from α-halogeno-ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003079</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3079</fpage>
<lpage>3084</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003079">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003079">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>One-step synthesis of an androcymbine-type compound</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Satoh</surname>
<given-names>F.</given-names></name>
<name><surname>Yagi</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3084</fpage>
<lpage>3088</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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, 1968</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003089</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3089</fpage>
<lpage>3113</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003089">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003089">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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, 1968</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39680003115</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>3115</fpage>
<lpage>3150</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39680003115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J39680003115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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/J3968000X001</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>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>X001</fpage>
<lpage>X003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J3968000X001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J3/J3968000X001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
</articles>
