<?xml version="1.0" encoding="utf-8"?>
<articles xmlns:xlink="http://www.w3.org/1999/xlink">
<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 catalytic dehydration of isomeric octadienols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000709</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spangler</surname>
<given-names>Charles W.</given-names></name>
<name><surname>Feldt</surname>
<given-names>Robert D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>709</fpage>
<lpage>710</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000709">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>Identification of steroids and triterpenes from a geological source by capillary gas–liquid chromatography and mass spectrometry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000710</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henderson</surname>
<given-names>W.</given-names></name>
<name><surname>Wollrab</surname>
<given-names>V.</given-names></name>
<name><surname>Eglinton</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>710</fpage>
<lpage>712</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000710">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000710">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>Nucleophilic substitution in octafluoro-9-fluorenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000713</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Spring</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>713</fpage>
<lpage>713</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000713">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000713">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 the five-co-ordinate complex, bromoazido-1,1,7,7-tetraethyldiethylenetriaminecopper(II)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000714</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dori</surname>
<given-names>Zvi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>714</fpage>
<lpage>714</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000714">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000714">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>π-Bonding in the boron–oxygen bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000715</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lanthier</surname>
<given-names>G. F.</given-names></name>
<name><surname>Graham</surname>
<given-names>W. A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>715</fpage>
<lpage>715</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000715">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000715">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 ketonic complex of acetylacetone with cobalt(II) bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nakamura</surname>
<given-names>Yukio</given-names></name>
<name><surname>Kawaguchi</surname>
<given-names>Shinichi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>716</fpage>
<lpage>716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000716">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>Decomposition of phenylpropioloyl peroxide and t-butyl peroxyphenylpropiolate in solution. A new type of induced decomposition</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000717</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muramoto</surname>
<given-names>N.</given-names></name>
<name><surname>Ochiai</surname>
<given-names>T.</given-names></name>
<name><surname>Simamura</surname>
<given-names>O.</given-names></name>
<name><surname>Yoshida</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>717</fpage>
<lpage>717</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000717">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000717">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>3,4:5,6:9,10-Tribenzobicyclo[6,2,0]decapentaene. A (4&lt;i&gt;n&lt;/i&gt;+ 4&lt;i&gt;n&lt;/i&gt;)π-electron system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000719</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garratt</surname>
<given-names>P. J.</given-names></name>
<name><surname>Mitchell</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>719</fpage>
<lpage>720</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000719">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000719">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>Evidence for a π-donor effect in transition-metal alkyls from H–D coupling constants</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duncan</surname>
<given-names>J. D.</given-names></name>
<name><surname>Green</surname>
<given-names>J. C.</given-names></name>
<name><surname>Green</surname>
<given-names>M. L. H.</given-names></name>
<name><surname>McLauchlan</surname>
<given-names>K. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>721</fpage>
<lpage>722</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000721">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 formation of an anthracene from 4,4′-diethoxycarbonylstilbene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000722</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>S. D.</given-names></name>
<name><surname>Mijovic</surname>
<given-names>M. V.</given-names></name>
<name><surname>Newman</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>722</fpage>
<lpage>723</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000722">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000722">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 remarkable basicity of 1,8-bis(dimethylamino)naphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000723</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alder</surname>
<given-names>R. W.</given-names></name>
<name><surname>Bowman</surname>
<given-names>P. S.</given-names></name>
<name><surname>Steele</surname>
<given-names>W. R. S.</given-names></name>
<name><surname>Winterman</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>723</fpage>
<lpage>724</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000723">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000723">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>Formation of thiobenzophenones by the alkoxide cleavage of substituted diphenylmethyl phenyl disulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000724</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miotti</surname>
<given-names>U.</given-names></name>
<name><surname>Sinico</surname>
<given-names>A.</given-names></name>
<name><surname>Ceccon</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>724</fpage>
<lpage>726</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000724">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000724">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>Mechanistic crossover in substitution reactions of acetonitrile–boron halide adducts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackborow</surname>
<given-names>J. R.</given-names></name>
<name><surname>Lockhart</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>726</fpage>
<lpage>727</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000726">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>Energetic metastable transitions in the mass spectrum of &lt;i&gt;s&lt;/i&gt;-triazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000727</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briggs</surname>
<given-names>P. R.</given-names></name>
<name><surname>Parker</surname>
<given-names>W. L.</given-names></name>
<name><surname>Shannon</surname>
<given-names>T. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>727</fpage>
<lpage>728</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000727">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000727">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>Isomeric 2′- and 3′-&lt;i&gt;O&lt;/i&gt;-acyl ribonucleoside derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000729</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Green</surname>
<given-names>D. P. L.</given-names></name>
<name><surname>Reese</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>729</fpage>
<lpage>731</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000729">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000729">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 base hydrolysis of methyl 2,3-diaminopropionate and its metal complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000732</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hay</surname>
<given-names>R. W.</given-names></name>
<name><surname>Morris</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>732</fpage>
<lpage>733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000732">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000732">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 mechanism of the reaction of low-valent metal complexes with electrophilic olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000733</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooke</surname>
<given-names>M.</given-names></name>
<name><surname>Green</surname>
<given-names>M.</given-names></name>
<name><surname>Wood</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>733</fpage>
<lpage>734</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000733">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 di-(4-vinylpyridine)copper dichloride. The polymerization of the vinyl group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000735</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laing</surname>
<given-names>Michael</given-names></name>
<name><surname>Horsfield</surname>
<given-names>Edgar</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>735</fpage>
<lpage>735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000735">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000735">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 mechanism of the rearrangement of havanensin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000737</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Okorie</surname>
<given-names>D. A.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>737</fpage>
<lpage>738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000737">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000737">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 absolute configuration of ambonic acid at C-25</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000738</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corsano</surname>
<given-names>Stefano</given-names></name>
<name><surname>Mincione</surname>
<given-names>Enrico</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>738</fpage>
<lpage>739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000738">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000738">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>Some metal complexes of 1,3-di-imines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Honeybourne</surname>
<given-names>C. L.</given-names></name>
<name><surname>Webb</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>739</fpage>
<lpage>740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000739">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>Nature of the isomerism in the adducts of diketen to non-aromatic 2-mercapto-1,3-diazaheterocycles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000741</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mammi</surname>
<given-names>M.</given-names></name>
<name><surname>Clemente</surname>
<given-names>D. A.</given-names></name>
<name><surname>Pra</surname>
<given-names>A. Del</given-names></name>
<name><surname>D'Angeli</surname>
<given-names>F.</given-names></name>
<name><surname>Veronese</surname>
<given-names>A. C.</given-names></name>
<name><surname>Toniolo</surname>
<given-names>C.</given-names></name>
<name><surname>Rigatti</surname>
<given-names>G.</given-names></name>
<name><surname>Coletta</surname>
<given-names>M.</given-names></name>
<name><surname>Boccalon</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>741</fpage>
<lpage>742</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000741">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000741">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>Carbon–phosphorus coupling in representative organophosphorus compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000742</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mavel</surname>
<given-names>G.</given-names></name>
<name><surname>Green</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>742</fpage>
<lpage>743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000742">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000742">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>Determination of the nuclear magnetic resonance parameters in &lt;i&gt;o&lt;/i&gt;-difluorobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000744</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Loemker</surname>
<given-names>J. E.</given-names></name>
<name><surname>Goldstein</surname>
<given-names>J. H.</given-names></name>
<name><surname>Read Jun. </surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>744</fpage>
<lpage>745</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000744">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000744">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>Charge-transfer interaction in triplet quenching of naphthalenes in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000745</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ander</surname>
<given-names>S.</given-names></name>
<name><surname>Blume</surname>
<given-names>H.</given-names></name>
<name><surname>Heinrich</surname>
<given-names>G.</given-names></name>
<name><surname>Schulte-Frohlinde</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>745</fpage>
<lpage>745</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000745">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000745">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>Acid-catalysed oxygen-18 exchange studies with oxalatobis-(2,2′-bipyridine)cobalt(III) and oxalatobis-(2,2′-bipyridine)chromium(III) cations in water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Broomhead</surname>
<given-names>J. A.</given-names></name>
<name><surname>Kane-Maguire</surname>
<given-names>N.</given-names></name>
<name><surname>Lauder</surname>
<given-names>I.</given-names></name>
<name><surname>Nimmo</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>747</fpage>
<lpage>748</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000747">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>Phosphorescence of benzophenone in fluid solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000749</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parker</surname>
<given-names>C. A.</given-names></name>
<name><surname>Joyce</surname>
<given-names>Thelma A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>749</fpage>
<lpage>750</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000749">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000749">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>Perfluorophenyl–silicon compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000750</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
<name><surname>Lynch</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>750</fpage>
<lpage>751</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000750">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000750">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>Stereochemistry of the oxidative addition of allylic halides to &lt;i&gt;trans&lt;/i&gt;-[IrCl(CO)(PMe&lt;sub&gt;2&lt;/sub&gt;Ph)&lt;sub&gt;2&lt;/sub&gt;]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000751</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deeming</surname>
<given-names>A. J.</given-names></name>
<name><surname>Shaw</surname>
<given-names>B. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>751</fpage>
<lpage>752</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000751">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000751">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>Conformational analysis by nuclear magnetic resonance. Interpretation of solvent effect on standard enthalpy and entropy differences between conformations of cyclohexanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000752</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Reisse</surname>
<given-names>J.</given-names></name>
<name><surname>Celotti</surname>
<given-names>J. C.</given-names></name>
<name><surname>Ottinger</surname>
<given-names>R.</given-names></name>
<name><surname>Chiurdoglu</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>752</fpage>
<lpage>754</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000752">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000752">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>Homo-&lt;i&gt;S&lt;/i&gt;′&lt;sub&gt;H&lt;/sub&gt; reactions on allylmethyl iodide leading to substituted cyclopropanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000754</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kaplan</surname>
<given-names>Leonard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>754</fpage>
<lpage>755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000754">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000754">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 sign and magnitude of the &lt;sup&gt;77&lt;/sup&gt;Se–&lt;sup&gt;195&lt;/sup&gt;Pt coupling constant</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000755</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McFarlane</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>755</fpage>
<lpage>756</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000755">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000755">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 photochemical rearrangement of 5-pyrazolidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000759</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eǧe</surname>
<given-names>Seyhan N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>759</fpage>
<lpage>760</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000759">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000759">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 laser Raman spectrum of nitrogen trichloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000760</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hendra</surname>
<given-names>P. J.</given-names></name>
<name><surname>Mackenzie</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>760</fpage>
<lpage>762</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000760">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000760">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 chromocyclomycin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berlin</surname>
<given-names>Yu. A.</given-names></name>
<name><surname>Kolosov</surname>
<given-names>M. N.</given-names></name>
<name><surname>Vasina</surname>
<given-names>I. V.</given-names></name>
<name><surname>Yartseva</surname>
<given-names>I. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>762</fpage>
<lpage>763</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000762">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 structures of trichododin and epinodosin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000763</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kubota</surname>
<given-names>Takashi</given-names></name>
<name><surname>Kubo</surname>
<given-names>Isao</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>763</fpage>
<lpage>764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000763">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000763">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>Cyclohexa-2,4-dienone–dienketen valence isomerisations: thermal and photochemical interconversions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000764</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hobson</surname>
<given-names>J. D.</given-names></name>
<name><surname>Holly</surname>
<given-names>M. M. Al</given-names></name>
<name><surname>Malpass</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>764</fpage>
<lpage>766</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000764">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000764">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>Hindered amines in peptide synthesis. Synthesis of 7-glycine-oxytocin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000766</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bodansky</surname>
<given-names>Miklos</given-names></name>
<name><surname>Bath</surname>
<given-names>Raymond J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>766</fpage>
<lpage>767</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000766">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000766">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>Oligonucleotide synthesis &lt;i&gt;via&lt;/i&gt; phosphotriester intermediates: the phenyl-protecting group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19680000767</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Reese</surname>
<given-names>C. B.</given-names></name>
<name><surname>Saffhill</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>767</fpage>
<lpage>768</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19680000767">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C19680000767">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>An unequivocal synthesis of dibenzo[&lt;i&gt;a&lt;/i&gt;,&lt;i&gt;l&lt;/i&gt;]pyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000718a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buu-Hoï</surname>
<given-names>N. P.</given-names></name>
<name><surname>Périn-Roussel</surname>
<given-names>Mrs. O.</given-names></name>
<name><surname>Jacquignon</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>718a</fpage>
<lpage>718a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000718a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000718a">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 stereochemistry of homo-allenyl participation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000718b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bertrand</surname>
<given-names>M.</given-names></name>
<name><surname>Santelli</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>718b</fpage>
<lpage>719</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000718b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000718b">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>Deoxygenation of 2-nitrophenyl phenyl sulphides by triethyl phosphite: a new aromatic rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000736a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Kulik</surname>
<given-names>S.</given-names></name>
<name><surname>Todd</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>736a</fpage>
<lpage>736a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000736a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000736a">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>Ring expansion during the reaction of simple aromatic nitro-compounds with triethyl phosphite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000736b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Mackie</surname>
<given-names>R. K.</given-names></name>
<name><surname>Todd</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>736b</fpage>
<lpage>737</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000736b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000736b">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 a copper–cytoside complex</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000746a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carrabine</surname>
<given-names>J. A.</given-names></name>
<name><surname>Sundaralingam</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>746a</fpage>
<lpage>746a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000746a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000746a">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 dihydrouracil: an unusual base of transfer ribonucleic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000746b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rohrer</surname>
<given-names>D.</given-names></name>
<name><surname>Sundaralingam</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>746b</fpage>
<lpage>747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000746b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000746b">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>Stepwise and catalytic &lt;i&gt;cis&lt;/i&gt;-hydrogenation of an alkyne under single phase conditions, including the isolation of an intermediate, an alkyne–transition metal hydride adduct</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000757a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Trocha-Grimshaw</surname>
<given-names>Mrs. J.</given-names></name>
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>757a</fpage>
<lpage>757a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000757a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000757a">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>Dicarbonyl-π-allylrhodium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1968000757b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Brien</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue>13</issue>
<fpage>757b</fpage>
<lpage>759</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1968000757b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/C1/C1968000757b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
</articles>
