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<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction of chromium compounds by molten potassium thiocyanate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000505</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kerridge</surname>
<given-names>D. H.</given-names></name>
<name><surname>Mosley</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>505</fpage>
<lpage>506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000505">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000505">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolytic desulphurization of dibenzoylstilbene episulphide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Padwa</surname>
<given-names>Albert</given-names></name>
<name><surname>Crumrine</surname>
<given-names>David</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>506</fpage>
<lpage>507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 reaction of a butadiene cyanide complex of nickel(I)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burnett</surname>
<given-names>M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>507</fpage>
<lpage>509</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 isolation of tris(pyridine)benzylchromium(III) chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sneeden</surname>
<given-names>R. P. A.</given-names></name>
<name><surname>Throndsen</surname>
<given-names>H. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>509</fpage>
<lpage>510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A palladium hydride and germyl–palladium complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000510</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooks</surname>
<given-names>E. H.</given-names></name>
<name><surname>Glockling</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>510</fpage>
<lpage>510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000510">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000510">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Two novel tetracyclo-octanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000511</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Freeman</surname>
<given-names>Peter K.</given-names></name>
<name><surname>Rao</surname>
<given-names>V. N. Mallikarjuna</given-names></name>
<name><surname>Bigam</surname>
<given-names>Glen E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>511</fpage>
<lpage>512</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000511">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000511">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hexaphenyltriapentafulvalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000512</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>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>512</fpage>
<lpage>513</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000512">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000512">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thio-sugars with sulphur in a seven-membered ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000513</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>J. M.</given-names></name>
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>513</fpage>
<lpage>515</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000513">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000513">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 structure of trigermylphosphine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000515</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cradock</surname>
<given-names>S.</given-names></name>
<name><surname>Davidson</surname>
<given-names>G.</given-names></name>
<name><surname>Ebsworth</surname>
<given-names>E. A. V.</given-names></name>
<name><surname>Woodward</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>515</fpage>
<lpage>516</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>On the formation and rearrangement of some benzocyclo-octatetraene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000516</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>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>516</fpage>
<lpage>516</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000516">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000516">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hemi-Dewar biphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000517</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burt</surname>
<given-names>G. D.</given-names></name>
<name><surname>Pettit</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>517</fpage>
<lpage>517</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000517">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000517">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nuclear magnetic resonance spectrum and conformation of poly-&lt;i&gt;γ&lt;/i&gt;-benzyl-L-glutamate in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000518</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marlborough</surname>
<given-names>D. I.</given-names></name>
<name><surname>Orrell</surname>
<given-names>K. G.</given-names></name>
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>518</fpage>
<lpage>519</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000518">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000518">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 study of monomer–dimer equilibrium in N–H bonds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mateos</surname>
<given-names>J. L.</given-names></name>
<name><surname>Cetina</surname>
<given-names>R.</given-names></name>
<name><surname>Chao</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>519</fpage>
<lpage>520</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Diels–Alder reaction of &lt;i&gt;o&lt;/i&gt;-benzoquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000520</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Gosden</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>520</fpage>
<lpage>521</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000520">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000520">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrylium salts as initiators for vinyl polymerisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000522</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bawn</surname>
<given-names>C. E. H.</given-names></name>
<name><surname>Carruthers</surname>
<given-names>R.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>522</fpage>
<lpage>523</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000522">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000522">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular catalysis in acetal hydrolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000523</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>Brian</given-names></name>
<name><surname>Smith</surname>
<given-names>M. Cecil</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>523</fpage>
<lpage>524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000523">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000523">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 2-chloro-2-nitrosobutane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>J. E.</given-names></name>
<name><surname>Rogers</surname>
<given-names>N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>524</fpage>
<lpage>525</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 abieslactone, a methoxy-tetracyclic triterpene lactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000525</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Matsunaga</surname>
<given-names>S.</given-names></name>
<name><surname>Okada</surname>
<given-names>J.</given-names></name>
<name><surname>Uyeo</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>525</fpage>
<lpage>527</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000525">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000525">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 glaucine, &lt;i&gt;O&lt;/i&gt;-methylcorydine, and pseudocorydine &lt;i&gt;via&lt;/i&gt; phenolic oxidative coupling</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000528</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shamma</surname>
<given-names>Maurice</given-names></name>
<name><surname>Slusarchyk</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>528</fpage>
<lpage>529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000528">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000528">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hofmann–Martius rearrangement of &lt;i&gt;N&lt;/i&gt;-methylnaphthylinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Russelll</surname>
<given-names>G. J.</given-names></name>
<name><surname>Topsom</surname>
<given-names>R. D.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>529</fpage>
<lpage>530</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The oxidising properties of alumina: the production of nitric oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000530</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parkyns</surname>
<given-names>N. D.</given-names></name>
<name><surname>Patterson</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>530</fpage>
<lpage>531</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000530">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000530">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A new synthetic method for exocyclic methylene αβ-unsaturated &lt;i&gt;γ&lt;/i&gt;- lactones and synthesis of (±)-isoalantolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000531</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>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>531</fpage>
<lpage>532</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000531">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000531">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vibronic intensity in hexa-aminecobalt(III) ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000532</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wentworth</surname>
<given-names>R. A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>532</fpage>
<lpage>533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000532">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000532">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anomalous optical rotatory dispersion of flavine nucleotides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000533</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gascoigne</surname>
<given-names>I. M.</given-names></name>
<name><surname>Radda</surname>
<given-names>G. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>533</fpage>
<lpage>535</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000533">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000533">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 Gibberellic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000535</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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>535</fpage>
<lpage>536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000535">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000535">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>4-Pyrones from enamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000536</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>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>536</fpage>
<lpage>536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Biosynthesis of the indole alkaloids: vindoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000537</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McCapra</surname>
<given-names>F.</given-names></name>
<name><surname>Money</surname>
<given-names>T.</given-names></name>
<name><surname>Scott</surname>
<given-names>A. I.</given-names></name>
<name><surname>Wright</surname>
<given-names>I. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>537</fpage>
<lpage>538</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000537">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000537">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mevalonoid nature of vindoline and reserpinine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000538</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goeggel</surname>
<given-names>H.</given-names></name>
<name><surname>Arigoni</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>538</fpage>
<lpage>539</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000538">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000538">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 dichloromethyl- and trichloromethyl-cyclohexadienones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000539</article-id><contrib-group><contrib contrib-type="author">
<name><surname>King</surname>
<given-names>J.</given-names></name>
<name><surname>Leaver</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>539</fpage>
<lpage>540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000539">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000539">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nature of the long-wavelength absorption bands of simple unsaturated chromophores</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mason</surname>
<given-names>S. F.</given-names></name>
<name><surname>Vane</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>540</fpage>
<lpage>541</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transannular hydride shifts. An application to the synthesis of &lt;i&gt;Lycopodium&lt;/i&gt; alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000541</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayer</surname>
<given-names>W. A.</given-names></name>
<name><surname>Piers</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>541</fpage>
<lpage>542</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000541">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000541">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of benzenesulphonylcarbene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000542</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Roy</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>542</fpage>
<lpage>543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000542">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000542">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Complexes of azobenzenes and Schiff bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000543</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bagga</surname>
<given-names>M. M.</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>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>543</fpage>
<lpage>544</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000543">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000543">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular participation in ester hydrolysis by the diazonium group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000544</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Triggle</surname>
<given-names>D. J.</given-names></name>
<name><surname>Vickers</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>544</fpage>
<lpage>545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000544">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000544">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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. Participation by a neighbouring ketal group in a boron trifluoride-catalysed rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000545</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>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>545</fpage>
<lpage>545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structure of melanin derived from (±)-3,4-dihydroxy-[&lt;sup&gt;14&lt;/sup&gt;C,&lt;sup&gt;3&lt;/sup&gt;H]phenylalanine by oxidation with tyrosinase</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000546</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirby</surname>
<given-names>G. W.</given-names></name>
<name><surname>Ogunkoya</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>546</fpage>
<lpage>547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000546">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000546">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>New olefinic and acetylenic complexes of tungsten</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000547</article-id><contrib-group><contrib contrib-type="author">
<name><surname>King</surname>
<given-names>R. B.</given-names></name>
<name><surname>Fronzaglia</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>547</fpage>
<lpage>549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000547">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000547">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 1,3,5,-trinitrobenzene and aliphatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000549</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>M. R.</given-names></name>
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>549</fpage>
<lpage>550</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000549">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000549">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 9-hydroxymethyloctalin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000550</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hikino</surname>
<given-names>Yazuko</given-names></name>
<name><surname>Mayo</surname>
<given-names>P. de</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>550</fpage>
<lpage>551</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectrum of 5-phenyl-1,3,4-oxathiazol-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000551</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Senning</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>551</fpage>
<lpage>552</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000551">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000551">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cotton effect of isolated double bonds in steroidal olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000552</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yogev</surname>
<given-names>Amnon</given-names></name>
<name><surname>Mazur</surname>
<given-names>Yehuda</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>552</fpage>
<lpage>553</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000552">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000552">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A fused salt solvent for growing cadmium sulphide crystals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000553</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haworth</surname>
<given-names>Daniel T.</given-names></name>
<name><surname>Lake</surname>
<given-names>David P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>553</fpage>
<lpage>554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000553">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000553">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal structure of potassium heptafluoroprotactinate(V)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D.</given-names></name>
<name><surname>Smith</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>554</fpage>
<lpage>555</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular arylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000555</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tiecco</surname>
<given-names>Marcello</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>555</fpage>
<lpage>556</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000555">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000555">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anionic complexes of dithiocarboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000556</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fackler </surname>
<given-names>John P.</given-names></name>
<name><surname>Coucouvanis</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>556</fpage>
<lpage>557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000556">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000556">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The interconversion of some µ-alkylthio- and alkyl-trithiocarbonato-complexes of nickel</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000557</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bladon</surname>
<given-names>Peter</given-names></name>
<name><surname>Bruce</surname>
<given-names>Robert</given-names></name>
<name><surname>Knox</surname>
<given-names>Graham R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>557</fpage>
<lpage>559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000557">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000557">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</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 configuration of bezo[&lt;i&gt;c&lt;/i&gt;]phenanthrene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19650000559</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kemp</surname>
<given-names>C. M.</given-names></name>
<name><surname>Mason</surname>
<given-names>S. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>559</fpage>
<lpage>560</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19650000559">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C19650000559">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;sup&gt;63&lt;/sup&gt;Cu– and &lt;sup&gt;65&lt;/sup&gt;Cu–&lt;sup&gt;31&lt;/sup&gt;P spin–spin coupling in copper(I) trialkyl phosphite complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1965000561a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>King</surname>
<given-names>Roy W.</given-names></name>
<name><surname>Huttemann</surname>
<given-names>T. J.</given-names></name>
<name><surname>Verkade</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>561a</fpage>
<lpage>561a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1965000561a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C1965000561a">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Chemical Communications (London)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Novel syntheses of halogeno- and deoxy-sugars</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1965000561b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1965</year></pub-date>
<volume>1965</volume>
<issue>21</issue>
<fpage>561b</fpage>
<lpage>562</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1965000561b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1965/C1/C1965000561b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
</articles>
