<?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 isomeric phenylpyrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000345</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dickerman</surname>
<given-names>S. Carlton</given-names></name>
<name><surname>Feigenbaum</surname>
<given-names>William M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>345</fpage>
<lpage>346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000345">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000345">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 from a monoterpene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>A. R.</given-names></name>
<name><surname>Brown</surname>
<given-names>R. T.</given-names></name>
<name><surname>Knight</surname>
<given-names>J. A.</given-names></name>
<name><surname>Martin</surname>
<given-names>J. A.</given-names></name>
<name><surname>Plunkett</surname>
<given-names>A. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>346</fpage>
<lpage>347</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000346">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 monoterpene precursor in the biosynthesis of indole alkaloids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Loew</surname>
<given-names>P.</given-names></name>
<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>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>347</fpage>
<lpage>348</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000347">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>Concerning the terpenoid origin of indole alkaloids: biosynthetic mapping by direct mass spectrometry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000348</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>E. S.</given-names></name>
<name><surname>McCapra</surname>
<given-names>Frank</given-names></name>
<name><surname>Money</surname>
<given-names>T.</given-names></name>
<name><surname>Fukumoto</surname>
<given-names>K.</given-names></name>
<name><surname>Hanson</surname>
<given-names>J. R.</given-names></name>
<name><surname>Mootoo</surname>
<given-names>B. S.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. T.</given-names></name>
<name><surname>Scott</surname>
<given-names>A. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>348</fpage>
<lpage>350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000348">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000348">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 gas-phase hydrogen bromide-catalysed decomposition of trimethylacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000350</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cross</surname>
<given-names>J. T. D.</given-names></name>
<name><surname>Stimson</surname>
<given-names>V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>350</fpage>
<lpage>351</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000350">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000350">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>Steric effects on the cyclisation of chalcone dibromides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Donnelly</surname>
<given-names>D. J.</given-names></name>
<name><surname>Donnelly</surname>
<given-names>J. A.</given-names></name>
<name><surname>Murphy</surname>
<given-names>J. J.</given-names></name>
<name><surname>Philbin</surname>
<given-names>E. M.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>(the late) T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>351</fpage>
<lpage>352</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000351">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 cyclo-adduct from &lt;i&gt;exo&lt;/i&gt;-3-phenyl-3,4,5-triazatricyclo[5,2,1,0&lt;sup&gt;2,6&lt;/sup&gt;]dec-4-ene and &lt;i&gt;p&lt;/i&gt;-bromophenyl isocyanate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000352</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>John E.</given-names></name>
<name><surname>Kapecki</surname>
<given-names>Jon A.</given-names></name>
<name><surname>Newton</surname>
<given-names>M. Gary</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>352</fpage>
<lpage>353</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000352">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000352">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>Mechanism of the photo-initiated addition of HBr to C&lt;sub&gt;2&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000353</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wong</surname>
<given-names>K. T.</given-names></name>
<name><surname>Armstrong</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>353</fpage>
<lpage>355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000353">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000353">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>Base-catalysed cyclisation of highly enolisable systems: diversion of pathway by magnesium chelation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Games</surname>
<given-names>D. E.</given-names></name>
<name><surname>Knight</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>355</fpage>
<lpage>357</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000355">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 control of pyrone and aromatic cylisation in polyketonic–polyenolic systems by magnesium alkoxide concentration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000357</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>James</surname>
<given-names>A. W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>357</fpage>
<lpage>359</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000357">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000357">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 anisotropies of the C–C, C–H, and CC bonds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000359</article-id><contrib-group><contrib contrib-type="author">
<name><surname>ApSimon</surname>
<given-names>J. W.</given-names></name>
<name><surname>Craig</surname>
<given-names>W. G.</given-names></name>
<name><surname>Demarco</surname>
<given-names>P. V.</given-names></name>
<name><surname>Mathieson</surname>
<given-names>D. W.</given-names></name>
<name><surname>Saunders</surname>
<given-names>L.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>359</fpage>
<lpage>361</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000359">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000359">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 n.m.r. spectra of some diterpenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000361</article-id><contrib-group><contrib contrib-type="author">
<name><surname>ApSimon</surname>
<given-names>J. W.</given-names></name>
<name><surname>Craig</surname>
<given-names>W. G.</given-names></name>
<name><surname>Demarco</surname>
<given-names>P. V.</given-names></name>
<name><surname>Mathieson</surname>
<given-names>D. W.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>361</fpage>
<lpage>363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000361">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000361">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 seven-membered-ring compounds: &lt;i&gt;X&lt;/i&gt;-ray analysis of dextrorotatory 4-bromo-6,10-dimethylbicyclo[5,3,0]decan-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000363</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sato</surname>
<given-names>T.</given-names></name>
<name><surname>Minato</surname>
<given-names>H.</given-names></name>
<name><surname>Shiro</surname>
<given-names>M.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>363</fpage>
<lpage>364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000363">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000363">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>Spectroscopic studies of the photodecomposition of silyl azides in argon matrices near 4°K: detection of iminosilicon, HNSi</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ogilvie</surname>
<given-names>J. F.</given-names></name>
<name><surname>Cradock</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>364</fpage>
<lpage>365</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000364">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 reaction of dimanganese decacarbonyl with triphenylphosphine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000366</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wawersik</surname>
<given-names>H.</given-names></name>
<name><surname>Basolo</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>366</fpage>
<lpage>367</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000366">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000366">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>Duality of mechanism in reactions of &lt;i&gt;o&lt;/i&gt;-halogenobenediazonium ions with sodium methoxide in methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000367</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bunnett</surname>
<given-names>J. F.</given-names></name>
<name><surname>Happer</surname>
<given-names>D. A. R.</given-names></name>
<name><surname>Takayama</surname>
<given-names>Hiroaki</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>367</fpage>
<lpage>368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000367">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000367">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 a natural 4,6-linked (+)-bileucofisetinidin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drewes</surname>
<given-names>S. E.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
<name><surname>Feeney</surname>
<given-names>J.</given-names></name>
<name><surname>Eggers</surname>
<given-names>S. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>368</fpage>
<lpage>369</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000368">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 biflavanols from black wattle bark: leucorobinetinidin-(+)-catechin and leucorobinetinidin-(+)-gallocatechin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000370</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Drewes</surname>
<given-names>S. E.</given-names></name>
<name><surname>Roux</surname>
<given-names>D. G.</given-names></name>
<name><surname>Saayman</surname>
<given-names>H. M.</given-names></name>
<name><surname>Feeney</surname>
<given-names>J.</given-names></name>
<name><surname>Eggers</surname>
<given-names>S. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>370</fpage>
<lpage>371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000370">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000370">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>Rapid infrared analysis of gas-chromatography peaks</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Low</surname>
<given-names>M. J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>371</fpage>
<lpage>372</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000371">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>Cyclopropyldiazomethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000372</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moss</surname>
<given-names>Robert A.</given-names></name>
<name><surname>Shulman</surname>
<given-names>Franklyn C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>372</fpage>
<lpage>373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000372">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000372">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–chain tautomerism of derivatives of &lt;i&gt;o&lt;/i&gt;-hydroxybenzylamine with aromatic aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000374</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McDonagh</surname>
<given-names>Antony F.</given-names></name>
<name><surname>Smith</surname>
<given-names>Howard E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>374</fpage>
<lpage>374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000374">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000374">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 degree of inclination between the two cyclopentadienyl rings in a dibridged ferrocene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000377</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>377</fpage>
<lpage>378</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000377">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000377">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 solvent-induced change in intensity of electronic absorption and circular dichroism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000378</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boudreaux</surname>
<given-names>E. A.</given-names></name>
<name><surname>Weigang </surname>
<given-names>O. E.</given-names></name>
<name><surname>Turner</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>378</fpage>
<lpage>380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000378">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000378">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>Organic synthesis by means of noble-metal compounds. Palladium-catalyzed carbonylation of amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tsuji</surname>
<given-names>J.</given-names></name>
<name><surname>Iwamoto</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>380</fpage>
<lpage>380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000380">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>Interpretation of the kinetics of acid-catalyzed reactions in water–glycerol mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000381</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schaleger</surname>
<given-names>L. L.</given-names></name>
<name><surname>Richards</surname>
<given-names>C. N.</given-names></name>
<name><surname>Watamori</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>381</fpage>
<lpage>382</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000381">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000381">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 bis-(&lt;i&gt;cis&lt;/i&gt;-1,2-diphenylethene-1,2-dithiolato)nickel</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000382</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sartain</surname>
<given-names>D.</given-names></name>
<name><surname>Truter</surname>
<given-names>Mary R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>382</fpage>
<lpage>383</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000382">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>Polyfluoroalkylation. The nucleophilic equivalent of Friedel–Crafts reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chambers</surname>
<given-names>R. D.</given-names></name>
<name><surname>Storey</surname>
<given-names>R. A.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>384</fpage>
<lpage>385</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000384">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 and general base catalysis by acetate ion in the hydrolysis of aryl acetates: substituent effects, solvent isotope effects, and entropies of activation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oakenfull</surname>
<given-names>D. G.</given-names></name>
<name><surname>Riley</surname>
<given-names>T.</given-names></name>
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>385</fpage>
<lpage>386</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000385">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 adsorption of metal–halogeno-complexes at metal–molten salt interfaces</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000386</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Narayan</surname>
<given-names>R.</given-names></name>
<name><surname>Lovering</surname>
<given-names>D.</given-names></name>
<name><surname>Inman</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>386</fpage>
<lpage>388</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000386">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000386">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>Empirical relationships between tetrahedral covalent radii and effective nuclear charge</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000388</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beagley</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>388</fpage>
<lpage>389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000388">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000388">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 π-inductive effect. Application to π-electron distributions in monosubstituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000390</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>David T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>390</fpage>
<lpage>391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000390">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000390">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>Mass spectra of polynuclear carbonyls: a new polynuclear carbonyl oxide of osmium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000391</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>B. F. G.</given-names></name>
<name><surname>Lewis</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>I. G.</given-names></name>
<name><surname>Wilson</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>391</fpage>
<lpage>392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000391">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000391">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>Corrigendum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C19660000392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>392</fpage>
<lpage>392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C19660000392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C19660000392">PDF</self-uri>
</article-meta>
</front>
<article-type>other</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 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/C1966000375a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Vingiello</surname>
<given-names>Frank A.</given-names></name>
<name><surname>Yanez</surname>
<given-names>Jose</given-names></name>
<name><surname>Greenwood</surname>
<given-names>Edward J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>375a</fpage>
<lpage>375a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1966000375a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C1966000375a">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>Nuclear magnetic resonance studies of rate processes and conformations. Ring inversion in two nitrogen-containing heterocyclic systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/C1966000375b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Riddell</surname>
<given-names>F. G.</given-names></name>
<name><surname>Lehn</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1966</year></pub-date>
<volume>1966</volume>
<issue>12</issue>
<fpage>375b</fpage>
<lpage>377</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=C1966000375b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1966/C1/C1966000375b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
</articles>
