<?xml version="1.0" encoding="utf-8"?>
<articles xmlns:xlink="http://www.w3.org/1999/xlink">
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Contents pages</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J397000FP007</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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>P007</fpage>
<lpage>P010</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J397000FP007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J397000FP007">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>Limonoids from &lt;i&gt;Khaya anthotheca&lt;/i&gt;(Welw.) C.DC.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000205</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adesogan</surname>
<given-names>E. K.</given-names></name>
<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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>205</fpage>
<lpage>211</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000205">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000205">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;Xylocarpus granatum&lt;/i&gt; Koenig</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000211</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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>211</fpage>
<lpage>213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XX. Thermal rearrangement of 5-(&lt;i&gt;p&lt;/i&gt;-substituted phenyl)-2(and 4)-methoxypyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000214</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Lee</surname>
<given-names>T.-C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>214</fpage>
<lpage>219</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000214">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000214">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 a functionalized isoprene unit to an allyl alcohol. Part II. Reactions with furylmethanol and thienylmethanol and synthesis of torreyal and dendrolasin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000220</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thomas</surname>
<given-names>Alan F.</given-names></name>
<name><surname>Ozainne</surname>
<given-names>Michel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>220</fpage>
<lpage>224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000220">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000220">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;-acetyl-&lt;i&gt;N&lt;/i&gt;-trichloromethylsulphenylarenesulphonamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brans</surname>
<given-names>R.</given-names></name>
<name><surname>Cremlyn</surname>
<given-names>R. J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>225</fpage>
<lpage>227</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis of 4,6-dihydroxyisophthalaldehyde and the 5-methyl and 5-methoxy-derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Worden</surname>
<given-names>Leonard R.</given-names></name>
<name><surname>Kaufman</surname>
<given-names>Kurt D.</given-names></name>
<name><surname>Smith</surname>
<given-names>Patricia J.</given-names></name>
<name><surname>Widiger</surname>
<given-names>Gary N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>227</fpage>
<lpage>230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Dimroth rearrangement. Part XII. Transformation by alkali of 4-amino-3-benzyl-1,2,3-triazole and its 5-substituted derivatives into the corresponding 4-benzylamino isomers. Retrogression of this reaction in neutral solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000230</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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>230</fpage>
<lpage>235</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVI. Synthesis of methyl natural bixin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000235</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pattenden</surname>
<given-names>Gerald</given-names></name>
<name><surname>Way</surname>
<given-names>(Mrs) J. E.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>235</fpage>
<lpage>241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXVII. Conversion of fucoxanthin into paracentrone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hora</surname>
<given-names>J.</given-names></name>
<name><surname>Toube</surname>
<given-names>T. P.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>241</fpage>
<lpage>242</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal rearrangement of 3-benzoyl-2,1-benzisoxazole to 2-phenyl-4&lt;i&gt;H&lt;/i&gt;-3,1-benzoxazone in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000242</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pinkus</surname>
<given-names>Jack L.</given-names></name>
<name><surname>Jessup</surname>
<given-names>Howard A.</given-names></name>
<name><surname>Cohen</surname>
<given-names>Theodore</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>242</fpage>
<lpage>244</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000242">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000242">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXXX. Preparation of 2- and 16-oxo-, and 3,16- and 2,16-dioxo-5α-androstane, and 2-oxo-5α-cholestane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000244</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bridgeman</surname>
<given-names>J. E.</given-names></name>
<name><surname>Butchers</surname>
<given-names>C. E.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Kasal</surname>
<given-names>A.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Woodgate</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>244</fpage>
<lpage>250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000244">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000244">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microbiological hydroxylation of steroids. Part I. Proton magnetic resonance spectra of ketones, alcohols, and acetates in the androstane, pregnane, and œstrane series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000250</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bridgeman</surname>
<given-names>J. E.</given-names></name>
<name><surname>Cherry</surname>
<given-names>P. C.</given-names></name>
<name><surname>Clegg</surname>
<given-names>A. S.</given-names></name>
<name><surname>Evans</surname>
<given-names>J. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Kasal</surname>
<given-names>A.</given-names></name>
<name><surname>Kumar</surname>
<given-names>V.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Morisawa</surname>
<given-names>Y.</given-names></name>
<name><surname>Richards</surname>
<given-names>(Mrs.) E. E.</given-names></name>
<name><surname>Woodgate</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>250</fpage>
<lpage>257</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000250">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000250">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 free-radical addition reactions of pin-2-ene, pin-2(10)-ene, and thuj-4(10)-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000258</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Claisse</surname>
<given-names>J. A.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
<name><surname>Parfitt</surname>
<given-names>L. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>258</fpage>
<lpage>262</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000258">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000258">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 assignments of some 2,2,4-trisubstituted 1,3-dioxolans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000263</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Inch</surname>
<given-names>T. D.</given-names></name>
<name><surname>Williams</surname>
<given-names>(Mrs.) N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>263</fpage>
<lpage>269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000263">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000263">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction of benzyl sulphonyl (sulphone) intermediates to sulphinic acids. Synthesis of hypotaurine, and of L-cysteine and L-homocysteine sulphinic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000270</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hope</surname>
<given-names>D. B.</given-names></name>
<name><surname>Morgan</surname>
<given-names>C. D.</given-names></name>
<name><surname>Wälti</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>270</fpage>
<lpage>273</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000270">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000270">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclopentadithiophenones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000273</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jordens</surname>
<given-names>P.</given-names></name>
<name><surname>Rawson</surname>
<given-names>G.</given-names></name>
<name><surname>Wynberg</surname>
<given-names>Hans</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>273</fpage>
<lpage>277</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000273">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000273">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXIV. Synthesis of ochratoxin A, a metabolite of &lt;i&gt;Aspergillus ochraceus&lt;/i&gt; Wilh.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000278</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
<name><surname>Woollven</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>278</fpage>
<lpage>281</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000278">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000278">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXV. Experiments directed towards a synthesis of aflatoxin-G2: synthesis of the coumarino-lactone system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000281</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bycroft</surname>
<given-names>B. W.</given-names></name>
<name><surname>Hatton</surname>
<given-names>J. R.</given-names></name>
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>281</fpage>
<lpage>284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000281">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000281">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies related to the chemistry of melanins. Part VI. Syntheses of 3-carboxypyrrole-2-acetic acid, 3,5-dicarboxypyrrole-2-acetic acid, and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000285</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
<name><surname>Waggott</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>285</fpage>
<lpage>290</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000285">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000285">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;peri&lt;/i&gt;-Naphthotriazines and related compounds. Part II. Some acenaphthylene derivatives; their preparation and properties</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000290</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowerday</surname>
<given-names>P.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
<name><surname>Arthur</surname>
<given-names>A. R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>290</fpage>
<lpage>297</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000290">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000290">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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;peri&lt;/i&gt;-Naphthotriazines and related compounds. Part III. Some photochemical reactions: synthesis of 1-methylacenaphtho[5,6-&lt;i&gt;bc&lt;/i&gt;]pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000298</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowerday</surname>
<given-names>P.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>298</fpage>
<lpage>303</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazaindenes (azaindoles). Part II. Thermal indolisation of 3- and 4-pyridylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000303</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kelly</surname>
<given-names>A. H.</given-names></name>
<name><surname>Parrick</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>303</fpage>
<lpage>307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000303">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000303">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The minor anthraquinones of &lt;i&gt;Xanthoria parietina&lt;/i&gt;(L.) Beltram, the chlorination of parietin, and the synthesis of fragilin and 7-chloroemodin (‘AO-1’)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000307</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sargent</surname>
<given-names>M. V.</given-names></name>
<name><surname>Smith</surname>
<given-names>David O'N.</given-names></name>
<name><surname>Elix</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>307</fpage>
<lpage>311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000307">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000307">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Triterpenoids from &lt;i&gt;Entandrophragma cylindricum&lt;/i&gt; Sprague. Part I. Structures of sapelins A and B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
<name><surname>Yee</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>311</fpage>
<lpage>314</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XXXI. C&lt;sub&gt;14&lt;/sub&gt;-tetrahydropyranyl and other polyacetylenes from the compositae &lt;i&gt;Dahlia coccinea&lt;/i&gt; Cav. var. &lt;i&gt;coccinea&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chin</surname>
<given-names>C.</given-names></name>
<name><surname>Cutler</surname>
<given-names>(Miss) M. C.</given-names></name>
<name><surname>Jones</surname>
<given-names>Sir Ewart R. H.</given-names></name>
<name><surname>Lee</surname>
<given-names>J.</given-names></name>
<name><surname>Safe</surname>
<given-names>S.</given-names></name>
<name><surname>Thaller</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>314</fpage>
<lpage>322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cyclisation of ketone thiosemicarbazones. Part II. Derivatives of phenoxyacetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landquist</surname>
<given-names>Justus K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>323</fpage>
<lpage>324</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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-amino-1,2,3,4-tetrahydro-6-hydroxycarbazole, an analogue of 5-hydroxytryptamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000325</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coombes</surname>
<given-names>G. E. A.</given-names></name>
<name><surname>Harvey</surname>
<given-names>D. J.</given-names></name>
<name><surname>Reid</surname>
<given-names>S. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>325</fpage>
<lpage>326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000325">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000325">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 heterocyclic systems related to benzocycloheptene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>H. J.</given-names></name>
<name><surname>Main</surname>
<given-names>B. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>327</fpage>
<lpage>329</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 2,4-dihydroxy- and 1,3-dihydroxy-8-methylphenanthrene-9,10-quinones and their bearing on the structure of denticulatol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sargent</surname>
<given-names>M. V.</given-names></name>
<name><surname>Smith</surname>
<given-names>David O'N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>329</fpage>
<lpage>331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tertiary butyl phosphorus compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000332</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crofts</surname>
<given-names>P. C.</given-names></name>
<name><surname>Parker</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>332</fpage>
<lpage>336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 &lt;i&gt;Khaya madagascariensis&lt;/i&gt; Jumelle et Perrier</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000336</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>336</fpage>
<lpage>340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000336">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000336">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 cephalosporin antibiotics. Part XVI. Configurational and conformational analysis of deacetoxy-Δ&lt;sup&gt;2&lt;/sup&gt;- and -Δ&lt;sup&gt;3&lt;/sup&gt;-cephalosporins and their corresponding sulphoxide isomers by nuclear magnetic resonance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000340</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>R. D. G.</given-names></name>
<name><surname>Demarco</surname>
<given-names>Paul V.</given-names></name>
<name><surname>Murphy</surname>
<given-names>C. F.</given-names></name>
<name><surname>Spangle</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>340</fpage>
<lpage>344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000340">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000340">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The aluminium(III) complexes of hydroxy-flavones in absolute methanol. Part I. Ligands containing only one chelating site</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Porter</surname>
<given-names>L. J.</given-names></name>
<name><surname>Markham</surname>
<given-names>K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>344</fpage>
<lpage>349</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 LXIV. Influence of solvents upon the cotton effects of some ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000350</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>Wallis</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>350</fpage>
<lpage>360</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000350">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000350">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Plant gums of the genus &lt;i&gt;Khaya&lt;/i&gt;. Part IV. Major component of &lt;i&gt;Khaya ivorensis&lt;/i&gt; gum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000361</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Bhattacharjee</surname>
<given-names>A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>361</fpage>
<lpage>365</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000361">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000361">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Plant gums of the genus &lt;i&gt;Khaya&lt;/i&gt;. Part V. Further studies on &lt;i&gt;Khaya senegalensis&lt;/i&gt; gum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000365</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Bhattacharjee</surname>
<given-names>A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>365</fpage>
<lpage>369</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000365">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000365">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phytotoxic compounds produced by &lt;i&gt;Fusarium equiseti&lt;/i&gt;. Part IV. Fission of trichothecan-3α,4β-diols by manganese dioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000369</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawkins</surname>
<given-names>A. W.</given-names></name>
<name><surname>Grove</surname>
<given-names>John Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>369</fpage>
<lpage>375</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000369">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000369">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phytotoxic compounds produced by &lt;i&gt;Fusarium equiseti&lt;/i&gt;. Part V. Transformation products of 4β,15-diacetoxy-3α,7α-dihydroxy-12,13-epoxytrichothec-9-en-8-one and the structures of nivalenol and fusarenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000375</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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>375</fpage>
<lpage>378</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phytotoxic compounds produced by &lt;i&gt;Fusarium equiseti&lt;/i&gt;. Part VI. 4β,8α,15-Triacetoxy-12,13-epoxytrichothec-9-ene-3α,7α-diol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000378</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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>378</fpage>
<lpage>379</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000378">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000378">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrene. Part VI. Reaction of 6′-nitropapaverine and its analogue with triethyl phosphite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kametani</surname>
<given-names>T.</given-names></name>
<name><surname>Yamanaka</surname>
<given-names>T.</given-names></name>
<name><surname>Ogasawara</surname>
<given-names>K.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>380</fpage>
<lpage>381</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Configuration and rearrangements of homoproaporphines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000382</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>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>382</fpage>
<lpage>385</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000382">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 X. Structure revision of a so-called spirobiphosphole. The rearrangement of a tricycloallylidenephosphorane to a phosph(III)onin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000386</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waite</surname>
<given-names>N. E.</given-names></name>
<name><surname>Tebby</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>386</fpage>
<lpage>392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000386">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000386">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society 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 XVI. Biogenetic-type synthesis of xanthones from their benzophenone precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Locksley</surname>
<given-names>H. D.</given-names></name>
<name><surname>Murray</surname>
<given-names>I. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>392</fpage>
<lpage>398</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000392">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Overcrowded molecules. Part IV. Thermal and photochemical electrocyclic reactions of &lt;i&gt;trans&lt;/i&gt;-2-benzylidene-1-diphenylmethyleneindane and its 3-methyl derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000399</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heller</surname>
<given-names>H. G.</given-names></name>
<name><surname>Salisbury</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>399</fpage>
<lpage>402</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000399">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000399">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society C: Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of hexaiodobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J39700000403</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Steer</surname>
<given-names>Rosemary J.</given-names></name>
<name><surname>Watkins</surname>
<given-names>S. F.</given-names></name>
<name><surname>Woodward</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1970</year></pub-date>
<volume>1970</volume>
<issue>2</issue>
<fpage>403</fpage>
<lpage>408</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J39700000403">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1970/J3/J39700000403">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
</articles>
