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<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J296700FP001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J296700FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J296700FP001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J296700FP003</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J296700FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J296700FP003">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Statistical kinetics of polyesterification of adipic acid with pentaerythritol or trimethylol ethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gordon</surname>
<given-names>M.</given-names></name>
<name><surname>Scantlebury</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1</fpage>
<lpage>13</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The infrared spectra of some benzimidazoline-2-thiones and benzimidazol-2-yl sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000014</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>D.</given-names></name>
<name><surname>Ralph</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>14</fpage>
<lpage>15</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000014">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000014">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic displacements in substituted pyridine &lt;i&gt;N&lt;/i&gt;-oxides. Part III. The light-catalysed reaction between 4-nitropyridine 1-oxide and piperidine in ethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>15</fpage>
<lpage>16</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peroxides of elements other than carbon. Part XII. The autoxidation of optically active 1-phenylethylboronic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000017</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Roberts</surname>
<given-names>B. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>17</fpage>
<lpage>22</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000017">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000017">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The interaction of 1,3,5-trinitrobenzene with aliphatic amines in dimethyl sulphoxide solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000023</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>M. R.</given-names></name>
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>23</fpage>
<lpage>28</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000023">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000023">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Charge-transfer complexes. Part II. Complex formation between halogenomethanes and aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000028</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>K. M. C.</given-names></name>
<name><surname>Farmer</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>28</fpage>
<lpage>32</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Raman spectra of potassiodinitromethane and potassiodinitro[&lt;sup&gt;2&lt;/sup&gt;H&lt;sub&gt;1&lt;/sub&gt;]-methane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lippincott</surname>
<given-names>E. R.</given-names></name>
<name><surname>Kenney</surname>
<given-names>T. E.</given-names></name>
<name><surname>Nanney</surname>
<given-names>T. R.</given-names></name>
<name><surname>Weiffenbach</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>32</fpage>
<lpage>33</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acidity of some methyl-substituted pyridinium ions in methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000033</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rochester</surname>
<given-names>C. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>33</fpage>
<lpage>36</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000033">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000033">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part VI. Boron trifluoride–aniline equilibria in ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Satchell</surname>
<given-names>R. S.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>36</fpage>
<lpage>41</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,3-Dipolar cycloaddition reactions of diazoalkanes. Part II. Kinetics of the thermal and photochemical formation of pyrazole from diazopropene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
<name><surname>Parry</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>41</fpage>
<lpage>42</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The calculation of –Δ&lt;i&gt;G&lt;/i&gt;° for axial–equatorial equilibria in monosubstituted cyclohexanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000043</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Charton</surname>
<given-names>M.</given-names></name>
<name><surname>Charton</surname>
<given-names>B. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>43</fpage>
<lpage>46</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000043">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000043">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The optical rotatory behaviour of lycorine and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000046</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kuriyama</surname>
<given-names>K.</given-names></name>
<name><surname>Iwata</surname>
<given-names>T.</given-names></name>
<name><surname>Moriyama</surname>
<given-names>M.</given-names></name>
<name><surname>Kotera</surname>
<given-names>K.</given-names></name>
<name><surname>Hamada</surname>
<given-names>Y.</given-names></name>
<name><surname>Mitsui</surname>
<given-names>R.</given-names></name>
<name><surname>Takeda</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>46</fpage>
<lpage>53</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000046">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000046">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The hydrolysis of ethyl vinyl ether. Part I. Reaction mechanism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kresge</surname>
<given-names>A. J.</given-names></name>
<name><surname>Chiang</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>53</fpage>
<lpage>57</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The hydrolysis of ethyl vinyl ether. Part II. Solvent isotope effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000058</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kresge</surname>
<given-names>A. J.</given-names></name>
<name><surname>Chiang</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>58</fpage>
<lpage>61</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000058">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000058">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the autoxidation of toluene catalysed by cobaltic acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000062</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morimoto</surname>
<given-names>T.</given-names></name>
<name><surname>Ogata</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>62</fpage>
<lpage>66</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000062">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000062">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organosilicon compounds. Part II. The methyl proton resonance spectra of methylphenyldisiloxanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000067</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Homer</surname>
<given-names>J.</given-names></name>
<name><surname>Jarvie</surname>
<given-names>A. W.</given-names></name>
<name><surname>Holt</surname>
<given-names>A.</given-names></name>
<name><surname>Hickton</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>67</fpage>
<lpage>71</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000067">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000067">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic study of the reactions of 1,1-diphenylallene in ethanol in the presence of sodium ethoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000071</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beltrame</surname>
<given-names>P.</given-names></name>
<name><surname>Pitea</surname>
<given-names>D.</given-names></name>
<name><surname>Marzo</surname>
<given-names>A.</given-names></name>
<name><surname>Simonetta</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>71</fpage>
<lpage>75</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000071">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000071">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Association of n-alcohols in non-polar solvents. Part I. The dielectric polarisations, apparent dipole moments, and near-infrared spectra of n-alcohols in carbon tetrachloride and cyclohexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000076</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ibbitson</surname>
<given-names>D. A.</given-names></name>
<name><surname>Moore</surname>
<given-names>L. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>76</fpage>
<lpage>79</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000076">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000076">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Association of n-alcohols in non-polar solvents. Part II. The dielectric polarisations, apparent dipole moments, and near-infrared spectra of n-alcohols in benzene and dioxan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000080</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ibbitson</surname>
<given-names>D. A.</given-names></name>
<name><surname>Moore</surname>
<given-names>L. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>80</fpage>
<lpage>83</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000080">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000080">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1-3-Dipolar cycloaddition reactions of diazoalkanes. Part III. Substituent effects on the kinetics of reactions between diazomethane and some unsaturated esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000083</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
<name><surname>Shih-Lin</surname>
<given-names>Yang</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>83</fpage>
<lpage>84</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tautomeric equilibrium constants for 3-amino- and 3-nitro-4-pyridone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>R. Alan</given-names></name>
<name><surname>Roney</surname>
<given-names>B. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>84</fpage>
<lpage>85</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ionisation of 4-nitrobenzyl cyanide in alkaline media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000085</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>85</fpage>
<lpage>87</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000085">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000085">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Catalysis by hydrogen halides in the gas phase. Part XII. Trimethylacetic acid and hydrogen bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000088</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>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>88</fpage>
<lpage>91</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electronic absorption spectrum of the α-1-adamantyl derivative of Michler's hydrol blue</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000091</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>91</fpage>
<lpage>92</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic reactions in melts and solids. Part IV. Hydrogenolysis of bromo-compounds by neat benzoin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000093</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Michman</surname>
<given-names>Michael</given-names></name>
<name><surname>Halpern</surname>
<given-names>Yuval</given-names></name>
<name><surname>Patai</surname>
<given-names>Saul</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>93</fpage>
<lpage>95</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000093">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000093">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photochemical reaction between diazomethane and 1,2-epoxypropane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>J. N.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>96</fpage>
<lpage>97</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The influence of solvent composition on the rates of &lt;i&gt;E&lt;/i&gt;2 elimination and similar reactions in alcohol–water mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000098</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckley</surname>
<given-names>P. D.</given-names></name>
<name><surname>England</surname>
<given-names>B. D.</given-names></name>
<name><surname>McLennan</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>98</fpage>
<lpage>101</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000098">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000098">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sesquiterpenoids. Part VI. The stereochemistry of desmotroposantonin: &lt;i&gt;X&lt;/i&gt;-ray analysis of 2-bromo-(–)-β-desmotroposantonin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000101</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McPhail</surname>
<given-names>A. T.</given-names></name>
<name><surname>Rimmer</surname>
<given-names>B.</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>101</fpage>
<lpage>106</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000101">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000101">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and physical properties of some 4-substituted 2,2′-bipyridyls and their 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000106</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>R. Alan</given-names></name>
<name><surname>Roney</surname>
<given-names>B. D.</given-names></name>
<name><surname>Sasse</surname>
<given-names>W. H. F.</given-names></name>
<name><surname>Wade</surname>
<given-names>K. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>106</fpage>
<lpage>111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000106">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000106">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of the cycloadducts formed by mono-bromo-&lt;i&gt;N&lt;/i&gt;-methoxycarbonylazepine and tetracyanoethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000112</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>Roger A.</given-names></name>
<name><surname>Baldwin</surname>
<given-names>John E.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>112</fpage>
<lpage>117</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and &lt;i&gt;X&lt;/i&gt;-ray analysis of 2,4,6-trimethyl-1,3,5-triselenan (triselenoparaldehyde) and of 2,4,6-trimethyl-1,3,5-dioxaselenan (monoselenoparaldehyde)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000117</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Credali</surname>
<given-names>L.</given-names></name>
<name><surname>Russo</surname>
<given-names>M.</given-names></name>
<name><surname>Mortillaro</surname>
<given-names>L.</given-names></name>
<name><surname>Checchi</surname>
<given-names>C. De</given-names></name>
<name><surname>Valle</surname>
<given-names>G.</given-names></name>
<name><surname>Mammi</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>117</fpage>
<lpage>118</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000117">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000117">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The use of radioisotopes in studies of reaction mechanism. Part I. Reaction order and activation parameters of iodide exchange in 1-iodo-2,4-dinitrobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000119</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kendall</surname>
<given-names>F. H.</given-names></name>
<name><surname>Miller</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>119</fpage>
<lpage>123</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000119">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000119">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,3,5-Triazines. Part VII. The ultraviolet, infrared, and &lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance spectra of some chloro-1,3,5-triazine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000123</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>R. A.</given-names></name>
<name><surname>Ward</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>123</fpage>
<lpage>126</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000123">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000123">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XII. The crystal structure of 2,6-dimethyl-1,4-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000127</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovich</surname>
<given-names>D.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>127</fpage>
<lpage>131</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000127">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000127">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XIII. The crystal structure of 2,3,5,6-tetramethyl-1,4-benzoquinone (duroquinone)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000131</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovich</surname>
<given-names>D.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
<name><surname>Ubell</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>131</fpage>
<lpage>139</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XIV. The crystal structure of 2,3-dimethyl-1,4-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000140</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovich</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>140</fpage>
<lpage>144</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000140">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000140">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XV. The solid-state photochemistry of &lt;i&gt;p&lt;/i&gt;-quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000144</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovich</surname>
<given-names>D.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>144</fpage>
<lpage>149</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000144">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000144">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the oxidation of the formate and deuterioformate ions by permanganate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000150</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Onwood</surname>
<given-names>D. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>150</fpage>
<lpage>152</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000150">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000150">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vapour phase spectra in the near-ultraviolet of some monosubstituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000153</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mangini</surname>
<given-names>A.</given-names></name>
<name><surname>Trombetti</surname>
<given-names>A.</given-names></name>
<name><surname>Zauli</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>153</fpage>
<lpage>165</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000153">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000153">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of santonin. Part IX. Kinetics of the alkaline hydrolysis of the lactone ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000165</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolt</surname>
<given-names>A. J. N.</given-names></name>
<name><surname>Carson</surname>
<given-names>(Miss) M. S.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>165</fpage>
<lpage>167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000165">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000165">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 measurements of equilibria involving hydration and hemiacetal formation from some carbonyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000169</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hooper</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>169</fpage>
<lpage>170</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000169">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000169">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Simple pyrimidines. Part IX. Deuterium exchange of &lt;i&gt;C&lt;/i&gt;-methyl protons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000171</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Batterham</surname>
<given-names>T. J.</given-names></name>
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Paddon-Row</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>171</fpage>
<lpage>173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homolytic mechanisms of aromatic rearrangements. Part I. The rearrangement of &lt;i&gt;N&lt;/i&gt;-chloroacetanilide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000174</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coulson</surname>
<given-names>Judith</given-names></name>
<name><surname>Williams</surname>
<given-names>Gareth H.</given-names></name>
<name><surname>Johnston</surname>
<given-names>K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>174</fpage>
<lpage>180</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000174">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000174">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electron spin resonance spectra of some hydroxylamine free radicals. Part III. Radicals formed by oxidations in alkaline solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000180</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Minor</surname>
<given-names>D. F.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
<name><surname>Ramsbottom</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>180</fpage>
<lpage>184</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000180">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000180">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 hydrolysis of glycofuranosides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000185</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>Brian</given-names></name>
<name><surname>Thacker</surname>
<given-names>David</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>185</fpage>
<lpage>189</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000185">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000185">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of 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/J29670000189</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Newton</surname>
<given-names>M. Gary</given-names></name>
<name><surname>Kapecki</surname>
<given-names>Jon A.</given-names></name>
<name><surname>Baldwin</surname>
<given-names>John E.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>189</fpage>
<lpage>194</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000189">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000189">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal structure of 10-dicyanomethyleneanthrone, an overcrowded aromatic compound</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000194</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Silverman</surname>
<given-names>J.</given-names></name>
<name><surname>Yannoni</surname>
<given-names>N. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>194</fpage>
<lpage>201</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000194">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000194">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Medium effects on rotational equilibria. Part III. The theory for any number of dipoles and its application to 1,1,2-trichloroethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
<name><surname>Cooper</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>202</fpage>
<lpage>205</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydride ion transfer in oxidations of alcohols and ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000205</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barter</surname>
<given-names>R. M.</given-names></name>
<name><surname>Littler</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>205</fpage>
<lpage>210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000205">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000205">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Infrared studies of terpenoid compounds. Part IV. Correlation of acidity and intramolecular hydrogen bonding for γ-hydroxy carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000211</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bennet</surname>
<given-names>W. S.</given-names></name>
<name><surname>Eglinton</surname>
<given-names>G.</given-names></name>
<name><surname>Fulke</surname>
<given-names>J. W. B.</given-names></name>
<name><surname>McCrindle</surname>
<given-names>R.</given-names></name>
<name><surname>Hirao</surname>
<given-names>K.</given-names></name>
<name><surname>Tahara</surname>
<given-names>A.</given-names></name>
<name><surname>Simon</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>211</fpage>
<lpage>215</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Absorption spectra of ketones. Part IX. Ultraviolet spectra and circular dichroism of bornenones and other βγ-unsaturated ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000215</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bays</surname>
<given-names>D. E.</given-names></name>
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>MacKenzie</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>215</fpage>
<lpage>226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000215">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000215">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Absorption spectra of ketones. Part X. Photochemical rearrangement of bicyclo[2,2,1]hepten-2-ones to bicyclo[3,2,0]hept-2-en-7-ones and their ultraviolet and circular-dichroic spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000226</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bays</surname>
<given-names>D. E.</given-names></name>
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>226</fpage>
<lpage>229</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000226">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000226">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XVI. The crystal structure of &lt;i&gt;trans&lt;/i&gt;-β-2-furylacrylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000229</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Filippakis</surname>
<given-names>S. E.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>229</fpage>
<lpage>232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000229">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000229">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XVII. The crystal structures of two modifications of &lt;i&gt;trans&lt;/i&gt;-β-2-thienylacrylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000233</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Block</surname>
<given-names>S.</given-names></name>
<name><surname>Filippakis</surname>
<given-names>S. E.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>233</fpage>
<lpage>238</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000233">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000233">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XVIII. The solid-state photochemistry of some heterocyclic analogues of &lt;i&gt;trans&lt;/i&gt;-cinnamic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000239</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lahav</surname>
<given-names>M.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>239</fpage>
<lpage>243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000239">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000239">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanisms of aromatic halogen substitution. Part XXV. The chlorination of 2-methylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000244</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cum</surname>
<given-names>G.</given-names></name>
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Lomas</surname>
<given-names>J. S.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>244</fpage>
<lpage>251</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000244">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000244">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanisms of aromatic halogen substitution. Part XXVI. Confirmation of the existence of a solvent deuterium isotope effect in the bromination of phenol in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000251</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Dusouqui</surname>
<given-names>O. M. H. El</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>251</fpage>
<lpage>252</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000251">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000251">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dissociation constants and infrared spectra of boron trifluoride complexes of substituted benzamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000253</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ellul</surname>
<given-names>B. M. J.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>253</fpage>
<lpage>255</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000253">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000253">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformation and reactivity. Part V. Kinetics of the esterification with diazodiphenylmethane in methanol, ethanol, or t-pentyl alcohol of the &lt;i&gt;trans&lt;/i&gt;-decalincarboxylic acids, of the 4-t-butyl- or 2-methyl-cyclohexanecarboxylic acids, of certain &lt;i&gt;trans&lt;/i&gt;-4-substituted cyclohexanecarboxylic acids, and of cyclohexanecarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000256</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Ehsan</surname>
<given-names>A.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
<name><surname>Toyne</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>256</fpage>
<lpage>260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000256">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000256">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effects of &lt;i&gt;π&lt;/i&gt;-electron densities and solvent on proton resonances of alkyl-substituted pyridines and benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chuck</surname>
<given-names>R. J.</given-names></name>
<name><surname>Randall</surname>
<given-names>E. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>261</fpage>
<lpage>265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A near-paradox of &lt;i&gt;E&lt;/i&gt;1&lt;i&gt;cb&lt;/i&gt;-like elimination in the 2-phenylethyl system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fraser</surname>
<given-names>G. M.</given-names></name>
<name><surname>Hoffmann</surname>
<given-names>H. M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>265</fpage>
<lpage>266</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic substitution. Part XVI. Reactivity of 3-isopropyl- and 3-cyclohexyl-pyridine and of nicotine towards phenyl-lithium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000267</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Poulton</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>267</fpage>
<lpage>269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000267">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000267">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 spectra of the dimers of hexafluoro- and 2,3,3,4,5-pentafluoro-cyclopentadiene: long-range &lt;sup&gt;19&lt;/sup&gt;F–&lt;sup&gt;19&lt;/sup&gt;F couplings</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000270</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fields</surname>
<given-names>R.</given-names></name>
<name><surname>Green</surname>
<given-names>M.</given-names></name>
<name><surname>Jones</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>270</fpage>
<lpage>272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000270">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000270">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of &lt;i&gt;N&lt;/i&gt;-heteroaromatic bases with nitrous acid. Part I. Diazotisation and nitrosation of α- and γ-amino-derivatives in dilute acid solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000273</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kalatzis</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>273</fpage>
<lpage>277</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000273">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000273">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of &lt;i&gt;N&lt;/i&gt;-heteroaromatic bases with nitrous acid. Part II. The kinetics of the diazotisation of 4-aminopyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000277</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kalatzis</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>277</fpage>
<lpage>282</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000277">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000277">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal decomposition of trifluoroacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Pritchard</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>282</fpage>
<lpage>286</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XIX. The crystal structure of monomethyl &lt;i&gt;trans&lt;/i&gt;,&lt;i&gt;trans&lt;/i&gt;-muconate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000286</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovich</surname>
<given-names>D.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>286</fpage>
<lpage>289</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000286">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000286">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XX. The crystal and molecular structures of dimethyl &lt;i&gt;trans&lt;/i&gt;,&lt;i&gt;trans&lt;/i&gt;-muconate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000290</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Filippakis</surname>
<given-names>S. E.</given-names></name>
<name><surname>Leiserowitz</surname>
<given-names>L.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>290</fpage>
<lpage>296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000290">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000290">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXI. The crystal and molecular structures of &lt;i&gt;trans&lt;/i&gt;,&lt;i&gt;trans&lt;/i&gt;-sorbamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000297</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Filippakis</surname>
<given-names>S. E.</given-names></name>
<name><surname>Leiserowitz</surname>
<given-names>L.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>297</fpage>
<lpage>304</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000297">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000297">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXII. The crystal and molecular structures of &lt;i&gt;trans&lt;/i&gt;,&lt;i&gt;trans&lt;/i&gt;-muconodinitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Filippakis</surname>
<given-names>S. E.</given-names></name>
<name><surname>Leiserowitz</surname>
<given-names>L.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>305</fpage>
<lpage>311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXIII. The solid-state photochemistry at 25° of some muconic acid derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000312</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lahav</surname>
<given-names>M.</given-names></name>
<name><surname>Schmidt</surname>
<given-names>G. M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>312</fpage>
<lpage>317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000312">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000312">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXIV. The luminescence properties of &lt;i&gt;N&lt;/i&gt;-salicylideneaniline and related anils in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>M. D.</given-names></name>
<name><surname>Flavian</surname>
<given-names>(Mrs.) S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>317</fpage>
<lpage>321</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXV. The absorption spectra of some &lt;i&gt;N&lt;/i&gt;-salicylideneanilines and related anils in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000321</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>M. D.</given-names></name>
<name><surname>Flavian</surname>
<given-names>(Mrs.) S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>321</fpage>
<lpage>328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000321">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000321">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXVI. The absorption spectra of some thermochromic &lt;i&gt;N&lt;/i&gt;-salicylideneanilines and hydroxynaphthylideneanilines in the crystal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>M. D.</given-names></name>
<name><surname>Flavian</surname>
<given-names>(Mrs.) S.</given-names></name>
<name><surname>Leiserowitz</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>329</fpage>
<lpage>334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXVII. The luminescence of crystalline &lt;i&gt;N&lt;/i&gt;-salicylideneanilines and related anils</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>M. D.</given-names></name>
<name><surname>Flavian</surname>
<given-names>(Mrs.) S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>334</fpage>
<lpage>340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electron spin resonance spectra of radicals formed from hydroxyl radicals and simple esters of formic, phosphorous, phosphoric, and methylphosphonic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000340</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Metcalfe</surname>
<given-names>A. R.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>340</fpage>
<lpage>343</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000340">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000340">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination–addition. Part X. Rates of addition of amines to &lt;i&gt;p&lt;/i&gt;-toly vinyl sulphone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000343</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McDowell</surname>
<given-names>S. T.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>343</fpage>
<lpage>348</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000343">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000343">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination–addition. Part XI. Electronic effects upon the reactivity of aryl vinyl sulphones towards amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000348</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McDowell</surname>
<given-names>S. T.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>348</fpage>
<lpage>350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000348">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000348">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination–addition. Part XII. Rates of addition of amines to alkenyl, allenyl, and alkynyl &lt;i&gt;p&lt;/i&gt;-tolyl sulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McDowell</surname>
<given-names>S. T.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>351</fpage>
<lpage>355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The molecular and crystal structure of bromomexicanin-E (C&lt;sub&gt;14&lt;/sub&gt;H&lt;sub&gt;15&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;Br)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>355</fpage>
<lpage>359</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XVIII. The kinetics and mechanisms of the reactions of dimethylketen, isobutyric anhydride, and isobutyryl halides with anilines in ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000360</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lillford</surname>
<given-names>P. J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>360</fpage>
<lpage>365</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000360">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000360">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XIX. Equilibria and acetylation in the system diacetyl sulphide–hydrogen chloride–acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000365</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hipkin</surname>
<given-names>J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>365</fpage>
<lpage>366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000365">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000365">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XX. The comparative acylation of phenols and thiols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000367</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hipkin</surname>
<given-names>J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>367</fpage>
<lpage>368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000367">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000367">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The additivity principle. Nitration and acetoxylation of some methylbenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
<name><surname>Wright</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>368</fpage>
<lpage>372</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000368">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular photoelectron spectroscopy. Part VI. Water, methanol, methane, and ethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Joboury</surname>
<given-names>M. I.</given-names></name>
<name><surname>Turner</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>373</fpage>
<lpage>376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reduction of 9,10-anthraquinones. Part I. Kinetic currents on polarography of 2-hydroxy-9,10-anthraquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000376</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Broadbent</surname>
<given-names>A. D.</given-names></name>
<name><surname>Sommermann</surname>
<given-names>E. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>376</fpage>
<lpage>378</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000376">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000376">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part X. An investigation of some aliphatic semidione and protonated semidione radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000378</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Pritchett</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>378</fpage>
<lpage>384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000378">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000378">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The &lt;sup&gt;19&lt;/sup&gt;F nuclear magnetic resonance spectra of &lt;i&gt;para&lt;/i&gt;-bonded isomers of the diethoxytetrafluorobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cavalli</surname>
<given-names>Luciano</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>384</fpage>
<lpage>387</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>N.m.r. Studies of rate processes and conformations. Part VI. Ring inversion in hexahydro-1,3,5-triazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000387</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lehn</surname>
<given-names>J. M.</given-names></name>
<name><surname>Riddell</surname>
<given-names>F. G.</given-names></name>
<name><surname>Price</surname>
<given-names>B. J.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>I. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>387</fpage>
<lpage>390</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000387">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000387">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Interaction of trialkyl phosphates and boron tribromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000390</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>H. R.</given-names></name>
<name><surname>Kelsall</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>390</fpage>
<lpage>392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000390">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000390">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mass spectra and organic analysis. Part VIII. The mass spectra of piperitone, the piperitols, and related products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thomas</surname>
<given-names>A. F.</given-names></name>
<name><surname>Willhalm</surname>
<given-names>B.</given-names></name>
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>392</fpage>
<lpage>400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000392">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermodynamic constants of the ionisation of the acid imino-group of uridine 5′-monophosphate and poly-uridylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aylward</surname>
<given-names>N. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>401</fpage>
<lpage>403</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part VII. Equilibria between gallium trihalides and aniline bases in ether solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000403</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mohammad</surname>
<given-names>Ali</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>403</fpage>
<lpage>406</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000403">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000403">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Equilibrium constants of charge-transfer complexes determined from &lt;sup&gt;19&lt;/sup&gt;F nuclear magnetic resonance absorption measurements</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000406</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>N. M. D.</given-names></name>
<name><surname>Foster</surname>
<given-names>R.</given-names></name>
<name><surname>Fyfe</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>406</fpage>
<lpage>410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000406">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000406">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An electric moment study of 6-chloro-9-ethylpurine, 6-chloro-9-phenethylpurine, and 6-chloro-9-phenylpurine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chou</surname>
<given-names>T. C.</given-names></name>
<name><surname>Lin</surname>
<given-names>H. H.</given-names></name>
<name><surname>Varma</surname>
<given-names>Ravi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>410</fpage>
<lpage>411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ultraviolet spectra of the 5-methoxy-3,3-dimethyl and -1,3,3-trimethyl-3&lt;i&gt;H&lt;/i&gt;-indolium cations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahmed</surname>
<given-names>M.</given-names></name>
<name><surname>Robinson</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>411</fpage>
<lpage>413</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkyl iodides as a source of alkyl radicals. Part I. Mechanism of the gas-phase photolysis of isopropyl iodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000414</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Braslavsky</surname>
<given-names>S. E.</given-names></name>
<name><surname>Grotewold</surname>
<given-names>J.</given-names></name>
<name><surname>Lissi</surname>
<given-names>E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>414</fpage>
<lpage>415</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000414">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000414">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic compounds of multivalent iodine. Part II. Ultraviolet spectra of some iodo- and iodoxy-benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000416</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gakovic</surname>
<given-names>Z.</given-names></name>
<name><surname>Morgan</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>416</fpage>
<lpage>418</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000416">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000416">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of radical anions. Part IV. The dimerisation of the tolan radical anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000418</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dadley</surname>
<given-names>D.</given-names></name>
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>418</fpage>
<lpage>422</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000418">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000418">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ultraviolet photochemistry of derivatives of triphenylmethane. Part I. Measurement of the rate constants in the photolysis of triphenylmethyl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000422</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>H. G.</given-names></name>
<name><surname>Owen</surname>
<given-names>E. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>422</fpage>
<lpage>425</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000422">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000422">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Evidence for merging of mechanism in competing &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;2 and &lt;i&gt;E&lt;/i&gt;2 processes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000425</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fraser</surname>
<given-names>G. M.</given-names></name>
<name><surname>Hoffmann</surname>
<given-names>H. M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>425</fpage>
<lpage>427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000425">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000425">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Autoxidation of &lt;i&gt;N&lt;/i&gt;-alkyl-amides. Part II. &lt;i&gt;N&lt;/i&gt;-alkyl-amide hydroperoxides and di-&lt;i&gt;N&lt;/i&gt;-alkyl-amide peroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sagar</surname>
<given-names>B. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>428</fpage>
<lpage>439</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic studies of hydrogen exchange in substituted dialkylanilines. Part III. Thermodynamic relationships of exchange</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000440</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ling</surname>
<given-names>A. Campbell</given-names></name>
<name><surname>Kendall</surname>
<given-names>F. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>440</fpage>
<lpage>445</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000440">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000440">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic studies of hydrogen exchange in substituted dialkylanilines. Part IV. Isotope effects and reaction mechanism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000445</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ling</surname>
<given-names>A. Campbell</given-names></name>
<name><surname>Kendall</surname>
<given-names>F. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>445</fpage>
<lpage>449</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000445">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000445">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part IX. Covalent hydration in the neutral species of substituted quinazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000449</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. I. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>449</fpage>
<lpage>454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000449">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000449">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidations of organic compounds by cobaltic salts. Part VIII. The oxidation of benzyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000455</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>T. A.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>455</fpage>
<lpage>463</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000455">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000455">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidations of organic compounds by cobaltic salts. Part IX. The oxidations of di-isopropyl ether and di-2-chloroethyl ether</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000464</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>T. A.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>464</fpage>
<lpage>468</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000464">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000464">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rate correlations involving the linear combination of substituent parameters. Part II. Hydrolysis of aryl benzoates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000468</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Humffray</surname>
<given-names>A. A.</given-names></name>
<name><surname>Ryan</surname>
<given-names>J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>468</fpage>
<lpage>471</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000468">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000468">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The polycondensation of benzyl chloride in the presence of Lewis acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000471</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parker</surname>
<given-names>Derek B. V.</given-names></name>
<name><surname>Davies</surname>
<given-names>W. G.</given-names></name>
<name><surname>South</surname>
<given-names>K. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>471</fpage>
<lpage>477</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000471">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000471">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics of unsymmetrical quinone–hydroquinone redox reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000477</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carter</surname>
<given-names>S.</given-names></name>
<name><surname>Murrell</surname>
<given-names>J. N.</given-names></name>
<name><surname>Rosch</surname>
<given-names>(the late) E. J.</given-names></name>
<name><surname>Trinajstić</surname>
<given-names>N.</given-names></name>
<name><surname>Wyatt</surname>
<given-names>P. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>477</fpage>
<lpage>484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000477">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000477">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polarographic current–voltage curves of fluorescein. Part I. Effect of pressure-head of mercury on mean current</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000484</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bannerjee</surname>
<given-names>N. R.</given-names></name>
<name><surname>Vig</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>484</fpage>
<lpage>486</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000484">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000484">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part X. Steric requirements of the nitrogen lone pair from aza-&lt;i&gt;cis&lt;/i&gt;-decalin equilibria</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000487</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>Kevan</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Waring</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>487</fpage>
<lpage>492</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000487">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000487">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XI. The conformation of 1-methylpiperidines from electric dipole moment studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000493</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bishop</surname>
<given-names>R. J.</given-names></name>
<name><surname>Sutton</surname>
<given-names>L. E.</given-names></name>
<name><surname>Dineen</surname>
<given-names>D.</given-names></name>
<name><surname>Jones</surname>
<given-names>Richard A. Y.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Wyatt</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>493</fpage>
<lpage>498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000493">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000493">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XII. Conformations of 1-alkyl-4-t-butylpiperazines from electric dipole moment studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Imbach</surname>
<given-names>J.-L.</given-names></name>
<name><surname>Jones</surname>
<given-names>Richard A. Y.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Wyatt</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>499</fpage>
<lpage>501</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XIII. The orientation of quaternised piperidines by the lactone formation method</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000501</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dorn</surname>
<given-names>H.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Nesbit</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>501</fpage>
<lpage>503</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000501">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000501">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability: the molar Kerr constants of allyl halides as solutes in carbon tetrachloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000503</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chen</surname>
<given-names>C.-Y.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Paul</surname>
<given-names>(Miss) S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>503</fpage>
<lpage>506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000503">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000503">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An electron spin resonance study of γ-irradiated polycrystalline n-propanearsonic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadena Jun. </surname>
<given-names>D. G.</given-names></name>
<name><surname>Rowlands</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>506</fpage>
<lpage>508</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination reactions. Part I. Decomposition of menthyltrimethylammonium ion in strongly basic media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>M. A.</given-names></name>
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Loudon</surname>
<given-names>A. G.</given-names></name>
<name><surname>Waller</surname>
<given-names>F. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>509</fpage>
<lpage>513</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectra of alkyl sulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000513</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aplin</surname>
<given-names>R. T.</given-names></name>
<name><surname>Bailey</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>513</fpage>
<lpage>516</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000513">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000513">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The proton magnetic resonance spectra of some diazoles, triazoles, and tetrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000516</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Batterham</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>516</fpage>
<lpage>518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000516">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000516">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A tracer study of the reactions promoted by the decay of a tritium atom contained in the molecule of ethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aliprandi</surname>
<given-names>Bianca</given-names></name>
<name><surname>Cacace</surname>
<given-names>Fulvio</given-names></name>
<name><surname>Guarino</surname>
<given-names>Angelo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>519</fpage>
<lpage>522</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal decomposition of n-butyl vinyl ether. Part I. The inhibited reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000523</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bamkole</surname>
<given-names>T. O.</given-names></name>
<name><surname>Emovon</surname>
<given-names>E. U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>523</fpage>
<lpage>524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000523">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000523">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvation of ions. Part X. Kinetic and thermodynamic properties of bimolecular reactions between anions and cations and between dipoles in protic and dipolar aprotic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000525</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mac</surname>
<given-names>Y. C.</given-names></name>
<name><surname>Millen</surname>
<given-names>W. A.</given-names></name>
<name><surname>Parker</surname>
<given-names>A. J.</given-names></name>
<name><surname>Watts</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>525</fpage>
<lpage>530</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000525">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000525">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electron spin resonance spectra of radicals obtained by the addition of amino- and hydroxyl radicals to alkenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000530</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>W. E.</given-names></name>
<name><surname>Longster</surname>
<given-names>G. F.</given-names></name>
<name><surname>Myatt</surname>
<given-names>J.</given-names></name>
<name><surname>Todd</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>530</fpage>
<lpage>533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000530">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000530">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies of electron-transfer reactions with aliphatic nitro-compounds in aqueous media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000533</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>W. E.</given-names></name>
<name><surname>Longster</surname>
<given-names>G. F.</given-names></name>
<name><surname>Myatt</surname>
<given-names>J.</given-names></name>
<name><surname>Todd</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>533</fpage>
<lpage>535</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000533">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000533">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvent effects in nuclear magnetic resonance spectroscopy. Part X. Solvent shifts induced by benzene in &lt;i&gt;ortho&lt;/i&gt;- and &lt;i&gt;meta&lt;/i&gt;-substituted methoxybenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000535</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Ronayne</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>535</fpage>
<lpage>540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000535">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000535">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvent effects in nuclear magnetic resonance spectroscopy. Part XI. The mechanism of solvent shifts of proton resonances induced by benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ronayne</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>540</fpage>
<lpage>546</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism and thermodynamics of chlorine transfer among organochlorinating agents. Part II. Reversible disproportionation of chloramine-T</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000546</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Higuchi</surname>
<given-names>T.</given-names></name>
<name><surname>Ikeda</surname>
<given-names>K.</given-names></name>
<name><surname>Hussain</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>546</fpage>
<lpage>549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000546">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000546">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of chlorination of cresol by chloramine-T. Mediation by dichloramine-T</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000549</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Higuchi</surname>
<given-names>T.</given-names></name>
<name><surname>Hussain</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>549</fpage>
<lpage>552</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000549">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000549">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The circular dichroism and absolute configuration of Tröger's base</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000553</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mason</surname>
<given-names>S. F.</given-names></name>
<name><surname>Vane</surname>
<given-names>G. W.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Wells</surname>
<given-names>R. J.</given-names></name>
<name><surname>Whitehurst</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>553</fpage>
<lpage>556</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000553">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000553">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in decarboxylation. Part IV. The effect of alkyl substituents on the rate of gas-phase decarboxylation of some β&lt;i&gt;γ&lt;/i&gt;-unsaturated acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000557</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bigley</surname>
<given-names>D. B.</given-names></name>
<name><surname>May</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>557</fpage>
<lpage>559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000557">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000557">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic conformational analysis. Ring inversion in hexahydropyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000560</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Riddell</surname>
<given-names>F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>560</fpage>
<lpage>561</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of nucleic acids and their components. Part VI. The reactions of formaldehyde with cytosine, cytidine, and deoxycytidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000562</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewin</surname>
<given-names>S.</given-names></name>
<name><surname>Humphreys</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>562</fpage>
<lpage>565</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000562">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000562">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chlorination of αβ-unsaturated carbonyl compounds. Part I. The addition of chlorine to methyl &lt;i&gt;trans&lt;/i&gt;-cinnamate in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cabaleiro</surname>
<given-names>Mercedes C.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>565</fpage>
<lpage>570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformation and reactivity. Part VI. Kinetics of the acid-catalysed esterification in methanol of the &lt;i&gt;trans&lt;/i&gt;-decalincarboxylic acids, of the 4-t-butyl- or 2-methyl-cyclohexanecarboxylic acids, of certain &lt;i&gt;trans&lt;/i&gt;-4-substituted cyclohexanecarboxylic acids, and of cyclohexanecarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000570</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Ehsan</surname>
<given-names>A.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
<name><surname>Toyne</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>570</fpage>
<lpage>573</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000570">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000570">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformational changes in bridged anthracene and tetracene systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000573</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Price</surname>
<given-names>B. J.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>I. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>573</fpage>
<lpage>576</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000573">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000573">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cyclic organophosphorus compounds. Part VI. The hydrolysis of some 1,3,2-dioxaphospholans and 1,3,2-dioxaphosphorinans in aqueous alkali–dioxan solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edmundson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Lambie</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>577</fpage>
<lpage>581</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The stereoselective reduction of ketones by aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000581</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Sawdaye</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>581</fpage>
<lpage>583</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000581">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000581">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectrometry of semicarbazones of αβ-unsaturated aldehydes and ketones, and of some related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000583</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blythin</surname>
<given-names>D. J.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>583</fpage>
<lpage>589</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000583">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000583">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The tautomerism of 3-hydroxyisoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>D. A.</given-names></name>
<name><surname>Smith</surname>
<given-names>G. F.</given-names></name>
<name><surname>Wahid</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>590</fpage>
<lpage>595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The anisotropic polarisabilities of anthracene and several halogenated anthracenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000595</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radom</surname>
<given-names>L.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>595</fpage>
<lpage>598</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbonium-ion rearrangements in the addition of bromine to some olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000598</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>598</fpage>
<lpage>604</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000598">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000598">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of lead tetra-acetate. Part X. Mechanism of oxidative rearrangement of two 3,3,3-triarylpropenes with lead tetra-acetate and in the Prévost reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000604</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>604</fpage>
<lpage>611</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000604">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000604">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electron spin resonance spectra of some aromatic cyanide and isocyanide anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000612</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Longster</surname>
<given-names>G. F.</given-names></name>
<name><surname>Myatt</surname>
<given-names>J.</given-names></name>
<name><surname>Todd</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>612</fpage>
<lpage>615</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000612">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000612">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thiophen chemistry. Part XIII. Mass spectra of substituted thiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000616</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Lawesson</surname>
<given-names>S.-O.</given-names></name>
<name><surname>Nolde</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>616</fpage>
<lpage>621</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000616">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000616">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron impact studies. Part VIII. Mass spectra of substituted azobenzenes; aryl migration on electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Lewis</surname>
<given-names>G. E.</given-names></name>
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>621</fpage>
<lpage>628</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydride transfer reactions catalysed by metal complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Charman</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>629</fpage>
<lpage>632</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution at a saturated carbon atom. Part IX. One anion- and two anion-catalysed unimolecular acidolysis of pyridiomethylmercuric chloride ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000633</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coad</surname>
<given-names>J. R.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>633</fpage>
<lpage>637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000633">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000633">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The isolation of an intermediate in the tricyanovinylation of &lt;i&gt;NN&lt;/i&gt;-dimethylaniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000637</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Farrell</surname>
<given-names>P. G.</given-names></name>
<name><surname>Newton</surname>
<given-names>J.</given-names></name>
<name><surname>White</surname>
<given-names>R. F. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>637</fpage>
<lpage>640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000637">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000637">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The relative electron-releasing power of a singly bound, and the electron-attracting power of a doubly bound nitrogen atom when present in the same five-membered ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000641</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>641</fpage>
<lpage>647</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000641">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000641">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of reactions in heterocycles. Part II. Replacement of the methylsulphonyl group in substituted pyridines, pyridazines, and pyrazine by methoxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000648</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Brown</surname>
<given-names>W. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>648</fpage>
<lpage>652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of radical anions. Part V. Disproportionation of the radical anion of azobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Evans</surname>
<given-names>J. C.</given-names></name>
<name><surname>James</surname>
<given-names>C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>652</fpage>
<lpage>653</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXI. Kinetics and mechanism of the hydrolysis of acyl cyanides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000653</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hibbert</surname>
<given-names>F.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>653</fpage>
<lpage>660</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unsaturated monocyclic compounds. Part XLVIII. A study by nuclear magnetic resonance of the energy barrier for conformational interconversion in annulenes and dehydro-annulenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000660</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calder</surname>
<given-names>I. C.</given-names></name>
<name><surname>Garratt</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>660</fpage>
<lpage>662</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000660">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000660">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structure, spectra, photochemistry, and thermal reactions of the 4a,4b-dihydrophenanthrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000662</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muszkat</surname>
<given-names>K. A.</given-names></name>
<name><surname>Fischer</surname>
<given-names>Ernst</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>662</fpage>
<lpage>678</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000662">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000662">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A large nuclear magnetic resonance shielding involving a carbon–carbon bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000679</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Claisse</surname>
<given-names>J. A.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>679</fpage>
<lpage>680</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000679">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000679">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent effects in the hydrolysis of diazoacetophenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000680</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Leveson</surname>
<given-names>L. L.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>680</fpage>
<lpage>683</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000680">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000680">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal decomposition of tetramethyltetrazen and the addition of dimethylamino-radicals to ethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000684</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Good</surname>
<given-names>A.</given-names></name>
<name><surname>Thynne</surname>
<given-names>J. C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>684</fpage>
<lpage>685</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000684">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000684">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ionic dissociation of 4-substituted 2,6-dichlorophenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000686</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Leary</surname>
<given-names>G. J.</given-names></name>
<name><surname>Topsom</surname>
<given-names>R. D.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>686</fpage>
<lpage>687</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000686">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000686">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidations of organic compounds by cobaltic salts. Part X. The oxidation of aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000687</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>T. A.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>687</fpage>
<lpage>695</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000687">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000687">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivity in nucleophilic substitution. Part III. The acetolysis of 9-fluorenyl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000695</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cowell</surname>
<given-names>G. W.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>695</fpage>
<lpage>697</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000695">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000695">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivity in nucleophilic substitution. Part IV. A carbonyl elimination reaction of 9-fluorenyl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000697</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cowell</surname>
<given-names>G. W.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
<name><surname>Morris</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>697</fpage>
<lpage>700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000697">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000697">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivity in nucleophilic substitution. Part V. Solvolysis of diphenylmethyl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000700</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cowell</surname>
<given-names>G. W.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
<name><surname>Morris</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>700</fpage>
<lpage>701</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000700">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000700">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of the reactions of the anhydrosulphites of α-hydroxy-carboxylic acids. Part I. Polymerisation of anhydrosulphite of α-hydroxyisobutyric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000702</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>D. G. H.</given-names></name>
<name><surname>Tighe</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>702</fpage>
<lpage>709</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000702">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000702">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effects of substituents on the thermodynamic functions of ionisation of &lt;i&gt;meta&lt;/i&gt;-substituted phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000709</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>P. D.</given-names></name>
<name><surname>Hall</surname>
<given-names>F. M.</given-names></name>
<name><surname>Reece</surname>
<given-names>I. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>709</fpage>
<lpage>712</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000709">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enhanced long-range coupling constants in cyclic systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>712</fpage>
<lpage>716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactivity of the hydroxy-group of methyl β-D-glucopyranoside in the Koenigs–Knorr reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bills</surname>
<given-names>Alan M.</given-names></name>
<name><surname>Green</surname>
<given-names>John W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>716</fpage>
<lpage>720</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000716">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heat of formation of phenyl benzoate and related bond dissociation energies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000720</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adams</surname>
<given-names>G. P.</given-names></name>
<name><surname>Fine</surname>
<given-names>D. H.</given-names></name>
<name><surname>Gray</surname>
<given-names>Peter</given-names></name>
<name><surname>Laye</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>720</fpage>
<lpage>722</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000720">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000720">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part VIII. The validity of infrared carbonyl shifts as measures of Lewis acid strength. The interaction of Lewis acids and phenalen-1-one(perinaphthenone)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000723</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mohammad</surname>
<given-names>Ali</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
<name><surname>Satchell</surname>
<given-names>Mrs. R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>723</fpage>
<lpage>725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000723">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000723">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part IX. Equilibria between aluminium bromide and substituted anilines in ether solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mohammad</surname>
<given-names>Ali</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>726</fpage>
<lpage>727</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000726">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part X. The basicity of ketones towards Lewis acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000727</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mohammad</surname>
<given-names>Ali</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
<name><surname>Satchell</surname>
<given-names>(Mrs.) R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>727</fpage>
<lpage>729</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000727">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000727">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Equilibria in thiol–disulphide interchanges. Part V. Reaction of some aminoethanethiols with 4,4′-dithiobis(benzenesulphonic acid)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000729</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gorin</surname>
<given-names>George</given-names></name>
<name><surname>Doughty</surname>
<given-names>Gavin</given-names></name>
<name><surname>Gideon</surname>
<given-names>Rose</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>729</fpage>
<lpage>736</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000729">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000729">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of reactions in heterocycles. Part III. Replacement of the methylsulphonyl group from quinoline, isoquinoline, quinoxaline, cinnoline, and phthalazine by methoxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Brown</surname>
<given-names>W. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>736</fpage>
<lpage>740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The conformations of diphenyl ketone, dimesityl ketone, and mesityl phenyl ketone as solutes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000741</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Hoskins</surname>
<given-names>J. A.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radom</surname>
<given-names>L.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>741</fpage>
<lpage>743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000741">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000741">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steric hindrance and acidity. Part I. The effect of 2,6-di-t-butyl substitution on the acidity of phenols in methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000743</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rochester</surname>
<given-names>C. H.</given-names></name>
<name><surname>Rossall</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>743</fpage>
<lpage>748</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000743">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000743">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cinnolines. Part X. The site of protonation of cinnoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000748</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Chapman</surname>
<given-names>R. F.</given-names></name>
<name><surname>Ellis</surname>
<given-names>A. W.</given-names></name>
<name><surname>Lovesey</surname>
<given-names>A. C.</given-names></name>
<name><surname>Waite</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>748</fpage>
<lpage>755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000748">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000748">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXII. The mechanism of hydrolysis of acyl cyanides in concentrated aqueous acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000755</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hibbert</surname>
<given-names>F.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>755</fpage>
<lpage>757</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000755">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000755">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Potentially tautomeric pyridines. Part IX. The effect of chlorine substituents on pyridone–hydroxypyridine tautomerism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000758</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Rowe</surname>
<given-names>J. D.</given-names></name>
<name><surname>Roy</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>758</fpage>
<lpage>761</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000758">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000758">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on Girard hydrazones. Part III. Further kinetic studies on the hydrolysis of Girard hydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Masui</surname>
<given-names>Masaichiro</given-names></name>
<name><surname>Ohmori</surname>
<given-names>Hidenobu</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>762</fpage>
<lpage>771</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of lead tetra-acetate. Part XI. The oxidation of styrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000771</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>771</fpage>
<lpage>779</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000771">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000771">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rate factors for the detritiation of triptycene, 9,10-dihydroanthracene and &lt;i&gt;o&lt;/i&gt;-xylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000780</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
<name><surname>Wright</surname>
<given-names>G. J.</given-names></name>
<name><surname>Homes</surname>
<given-names>(Miss) A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>780</fpage>
<lpage>782</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000780">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000780">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular conformations. Part III. &lt;i&gt;X&lt;/i&gt;-ray analysis of 17aβ-&lt;i&gt;p&lt;/i&gt;-bromobenzenesulphonyloxy-17α-methyl-19-nor-9β,10α-D-homoandrost-4-en-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000783</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Puckett</surname>
<given-names>R. T.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
<name><surname>Cross</surname>
<given-names>A. D.</given-names></name>
<name><surname>Siddall</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>783</fpage>
<lpage>791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000783">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000783">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polymeric quinones. Part IV. Vicinal effects in polyquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000791</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hunt</surname>
<given-names>S. E.</given-names></name>
<name><surname>Lindsey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Savill</surname>
<given-names>N. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>791</fpage>
<lpage>796</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000791">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000791">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>High-resolution fluorine magnetic resonance spectra of pentafluoroanisole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000797</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawrenson</surname>
<given-names>I. J.</given-names></name>
<name><surname>Jones</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>797</fpage>
<lpage>799</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000797">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000797">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The &lt;i&gt;I&lt;/i&gt;&lt;sub&gt;π&lt;/sub&gt; effect and its consequences for the theoretical determination of properties of substituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000799</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Godfrey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>799</fpage>
<lpage>802</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000799">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000799">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthetic aspects of free-radical addition reactions. Part VI. The relative reactivities of ethyl malonate and related compounds towards oct-1-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000803</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Sharp</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>803</fpage>
<lpage>805</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000803">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000803">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvent effects in nuclear magnetic resonance spectroscopy. Part XII. Correlations between benzene-induced solvent shifts and structure in pyridines, quinolines, pyrroles, and indoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000805</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ronayne</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>805</fpage>
<lpage>808</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000805">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000805">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination–addition. Part XIII. Reactions of ω-bromoalkyl p-tolyl sulphones with bases: the role of inductive effects in elimination and substitution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000808</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knipe</surname>
<given-names>A. C.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>808</fpage>
<lpage>814</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000808">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000808">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The synthesis and aggregation of 9-phenyl- and 9-s-butyl-3,6-bisdimethylaminoacridine in solution. The dealkylation of 9-t-butylacridans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duuren</surname>
<given-names>B. L. Van</given-names></name>
<name><surname>Goldschmidt</surname>
<given-names>B. M.</given-names></name>
<name><surname>Seltzman</surname>
<given-names>H. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>814</fpage>
<lpage>819</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The conformations of six molecules containing the cyano-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000819</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
<name><surname>Stiles</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>819</fpage>
<lpage>824</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000819">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000819">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. Quinoxaline and some of its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000824</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hurley</surname>
<given-names>(Miss) J.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>824</fpage>
<lpage>827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000824">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000824">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rates of ionisation and enolisation of some aliphatic ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000827</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Hillier</surname>
<given-names>G. R.</given-names></name>
<name><surname>Mansfield</surname>
<given-names>J. W.</given-names></name>
<name><surname>Street</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>827</fpage>
<lpage>832</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000827">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000827">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dissociation of &lt;i&gt;N&lt;/i&gt;-(2,4-dinitrophenyl)benzylammonium ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Hartshorn</surname>
<given-names>M. P.</given-names></name>
<name><surname>Senanayake</surname>
<given-names>U. M.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>833</fpage>
<lpage>834</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nuclear magnetic resonance spectra of fluorobenzenes. Part I. The analysis of the ABB′XX′ and ABB′XX′R spectra of some 2-substituted 1,3-difluorobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000835</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
<name><surname>Macdonald</surname>
<given-names>D. B.</given-names></name>
<name><surname>Pepper</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>835</fpage>
<lpage>841</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000835">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000835">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A variable-temperature N.m.r. study of the ring inversion in 7,12-dihydropleiadene and its 1-methoxy-derivative using a quantitative treatment of the collapse of an AB quartet</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000841</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biffin</surname>
<given-names>M. E. C.</given-names></name>
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Connor</surname>
<given-names>T. M.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>841</fpage>
<lpage>846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000841">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000841">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ionic dissociation of 4-substituted phenols and 2,6-dichloro- and 2,6-dimethyl-phenols in organic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000846</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Leary</surname>
<given-names>G. J.</given-names></name>
<name><surname>Topsom</surname>
<given-names>R. D.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>846</fpage>
<lpage>851</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000846">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000846">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acid–base equilibria of substituted benzoic acids. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000852</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>J. M.</given-names></name>
<name><surname>Gore</surname>
<given-names>N. E.</given-names></name>
<name><surname>Sawbridge</surname>
<given-names>J. E.</given-names></name>
<name><surname>Cardenas-Cruz</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>852</fpage>
<lpage>859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000852">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000852">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformations of aromatic ethers as determined from their ultraviolet absorption spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>E. R.</given-names></name>
<name><surname>Williams</surname>
<given-names>S. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>859</fpage>
<lpage>866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics and mechanism of 1,3-cycloaddition of a substituted benzonitrile oxide to a series of arylacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000867</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beltrame</surname>
<given-names>P.</given-names></name>
<name><surname>Veglio</surname>
<given-names>C.</given-names></name>
<name><surname>Simonetta</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>867</fpage>
<lpage>873</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000867">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000867">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vibration-spectral studies of carboxylate ions. Part II. Substituted benzoate ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000874</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>874</fpage>
<lpage>879</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000874">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000874">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vibration-spectral studies of carboxylate ions. Part III. Sodium formate, HCO&lt;sub&gt;2&lt;/sub&gt;Na and DCO&lt;sub&gt;2&lt;/sub&gt;Na; Raman-spectral depolarisation ratios in aqueous solution, and band splitting in the solid-state infrared spectrum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000879</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>879</fpage>
<lpage>885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000879">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000879">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron-impact induced fragmentations of pyrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000885</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishiwaki</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>885</fpage>
<lpage>888</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000885">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000885">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic additions to alkenes. Part IV. Kinetics of the reaction of 2,4-dinitrobenzenesulphenyl bromide with cyclohexene in benzene and in chloroform solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>D. S.</given-names></name>
<name><surname>Hogg</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>889</fpage>
<lpage>892</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part X. The fragmentation of quinazolines under electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000892</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Batterham</surname>
<given-names>T. J.</given-names></name>
<name><surname>Triffett</surname>
<given-names>A. C. K.</given-names></name>
<name><surname>Wunderlich</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>892</fpage>
<lpage>897</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000892">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000892">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ultraviolet spectra of &lt;i&gt;O&lt;/i&gt;-(2,4-dinitrophenyl)oximes and 2,4-dinitrophenylhydrazones: transmission of electronic effects through O and NH groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000898</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
<name><surname>Sheradsky</surname>
<given-names>Tuvia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>898</fpage>
<lpage>903</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000898">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000898">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The influence of solvent on the reaction between isopropylamine and 2-(bromoacetyl)naphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000904</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>904</fpage>
<lpage>908</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000904">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000904">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic rearrangements. Part VIII. Attempted intramolecular oxygen-transfer in chlorofurazanobenzofuroxans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000909</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Gray</surname>
<given-names>A. C. Gripper</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>909</fpage>
<lpage>911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000909">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000909">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heterocyclic rearrangements. Part IX. The alkylation of benzofuroxans with formation of 1-hydroxybenzimidazole 3-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000911</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Gray</surname>
<given-names>A. C. Gripper</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>911</fpage>
<lpage>914</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000911">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000911">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;-oxides and related compounds. Part XXXI. The nuclear magnetic resonance spectra and tautomerism of some substituted benzofuroxans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000914</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Sewell</surname>
<given-names>M. J.</given-names></name>
<name><surname>Wallis</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>914</fpage>
<lpage>919</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000914">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000914">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton magnetic resonance spectra of methylated 5-aminotetrazole derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000919</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Butler</surname>
<given-names>R. N.</given-names></name>
<name><surname>Feeney</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>919</fpage>
<lpage>920</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000919">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000919">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Optically active co-ordination compounds. Part XI. Complexes of copper(II) with 2-aminopropanol and &lt;i&gt;Ψ&lt;/i&gt;-ephedrine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000921</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gillard</surname>
<given-names>R. D.</given-names></name>
<name><surname>Wootton</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>921</fpage>
<lpage>922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000921">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000921">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hindered rotation in &lt;i&gt;o&lt;/i&gt;-toluidine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000922</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Price</surname>
<given-names>B. J.</given-names></name>
<name><surname>Eggleston</surname>
<given-names>(Miss) J. A.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>I. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>922</fpage>
<lpage>925</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000922">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000922">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XI. Heterolytic fragmentations of hydroxycyclohexadienyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000926</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Pritchett</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>926</fpage>
<lpage>930</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000926">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000926">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The proton magnetic resonance spectra of porphyrins. Part V. Syntheses and spectra of some &lt;i&gt;meso&lt;/i&gt;-methylated porphyrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000930</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burbidge</surname>
<given-names>P. A.</given-names></name>
<name><surname>Collier</surname>
<given-names>G. L.</given-names></name>
<name><surname>Jackson</surname>
<given-names>A. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>930</fpage>
<lpage>937</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000930">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000930">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gas-phase reactions of halogenoalkylsilanes. Part IV. 1-Chloroethyl-diethylchlorosilane and 2-chloroethyltrialkylsilanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000937</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>I. M. T.</given-names></name>
<name><surname>Jones</surname>
<given-names>M. R.</given-names></name>
<name><surname>Pett</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>937</fpage>
<lpage>940</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000937">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000937">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in decarboxylation. Part V. Kinetic isotope effects in the gas-phase thermal decarboxylation of 2,2-dimethyl-4-phenylbut-3-enoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000941</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bigley</surname>
<given-names>D. B.</given-names></name>
<name><surname>Thurman</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>941</fpage>
<lpage>943</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The radiation chemistry of cystamine sulphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000944</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jayson</surname>
<given-names>G. G.</given-names></name>
<name><surname>Owen</surname>
<given-names>T. C.</given-names></name>
<name><surname>Wilbraham</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>944</fpage>
<lpage>949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000944">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000944">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the reversible addition of water to substituted quinazolines and some triazanaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000950</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bunting</surname>
<given-names>J. W.</given-names></name>
<name><surname>Perrin</surname>
<given-names>D. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>950</fpage>
<lpage>954</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000950">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000950">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of reactions in heterocycles. Part IV. The reaction of chloropurines and their 9-methyl derivatives with sodium ethoxide or piperidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000954</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>954</fpage>
<lpage>958</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000954">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000954">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics of the fast proton-transfer reactions between 2,4-dinitrophenol and some aliphatic amines in chlorobenzene solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000959</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caldin</surname>
<given-names>E. F.</given-names></name>
<name><surname>Crooks</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>959</fpage>
<lpage>961</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000959">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000959">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of organometallic compounds containing silicon. Part I. Reactions of dimethylphenyl-, methyldiphenyl-, and triphenyl-silyllithium with 1,1-diphenylethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000961</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Jones</surname>
<given-names>M. Ll.</given-names></name>
<name><surname>Rees</surname>
<given-names>N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>961</fpage>
<lpage>964</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000961">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000961">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanisms of elimination reactions. The effect of added dimethyl sulphoxide on rates, isotope effects, and substituent effects in the reaction of 2-arylethyldimethylsulphonium bromides with sodium hydroxide in water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000964</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cockerill</surname>
<given-names>Anthony F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>964</fpage>
<lpage>969</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000964">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000964">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The competitive oxidation of acetylene and propyne</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000970</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hay</surname>
<given-names>J. M.</given-names></name>
<name><surname>Lyon</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>970</fpage>
<lpage>973</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000970">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000970">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivity and structure of alkyl vinyl ethers. Part III. Kinetics and mechanism of dichlorocarbene addition reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000973</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
<name><surname>Woods</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>973</fpage>
<lpage>976</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000973">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000973">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of the reactions of the anhydrosulphites of α-hydroxy-carboxylic acids. Part II. Polymerisation of glycollic and lactic acid anhydrosulphites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000976</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>D. G. H.</given-names></name>
<name><surname>Tighe</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>976</fpage>
<lpage>980</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000976">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000976">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XII. Characteristics of the iminoxy-radicals from the 1-halogenofluorenone oximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000981</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilbert</surname>
<given-names>B. C.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>981</fpage>
<lpage>984</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000981">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000981">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Model calculations of primary hydrogen isotope effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000985</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Ferrall</surname>
<given-names>R. A. More</given-names></name>
<name><surname>Kouba</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>985</fpage>
<lpage>990</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000985">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000985">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemistry of organic nitrogen compounds. Part III. The formation of allenes and 1,3-dienes from pyrazolenines: a photochemical reaction involving ion-pairs</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670000991</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Day</surname>
<given-names>A. C.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>991</fpage>
<lpage>1003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670000991">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670000991">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Circular dichroism of 1,3-dithiolans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Cooper</surname>
<given-names>G. H.</given-names></name>
<name><surname>Hudec</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1004</fpage>
<lpage>1007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of olefin formation in the pyrolysis of n-butyl bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bridge</surname>
<given-names>M. R.</given-names></name>
<name><surname>Holmes</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1008</fpage>
<lpage>1010</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 anomerisation of methyl D-glucopyranosides and methyl D-glucofuranosides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001010</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>B.</given-names></name>
<name><surname>Thacker</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1010</fpage>
<lpage>1013</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001010">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001010">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the condensation of acetaldehyde with formaldehyde in aqueous alkaline solutions at 5–20°</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001013</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ogata</surname>
<given-names>Yoshiro</given-names></name>
<name><surname>Kawasaki</surname>
<given-names>Atsushi</given-names></name>
<name><surname>Yokoi</surname>
<given-names>Kenji</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1013</fpage>
<lpage>1020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001013">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001013">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inclusion compounds in perhydrotriphenylene. Part I. The crystal structure of perhydrotriphenylene and of some inclusion compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001020</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allegra</surname>
<given-names>G.</given-names></name>
<name><surname>Farina</surname>
<given-names>M.</given-names></name>
<name><surname>Immirzi</surname>
<given-names>A.</given-names></name>
<name><surname>Colombo</surname>
<given-names>A.</given-names></name>
<name><surname>Rossi</surname>
<given-names>U.</given-names></name>
<name><surname>Broggi</surname>
<given-names>R.</given-names></name>
<name><surname>Natta</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1020</fpage>
<lpage>1028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001020">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001020">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inclusion compounds in perhydrotriphenylene. Part II. The conformation of the included molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001028</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allegra</surname>
<given-names>G.</given-names></name>
<name><surname>Farina</surname>
<given-names>M.</given-names></name>
<name><surname>Colombo</surname>
<given-names>A.</given-names></name>
<name><surname>Casagrande-Tettamanti</surname>
<given-names>G.</given-names></name>
<name><surname>Rossi</surname>
<given-names>U.</given-names></name>
<name><surname>Natta</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1028</fpage>
<lpage>1033</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton magnetic resonance studies of citral a and b</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001033</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ohtsuru</surname>
<given-names>M.</given-names></name>
<name><surname>Teraoka</surname>
<given-names>M.</given-names></name>
<name><surname>Tori</surname>
<given-names>K.</given-names></name>
<name><surname>Takeda</surname>
<given-names>Ken'ichi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1033</fpage>
<lpage>1035</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001033">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001033">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic reactivity. Part XXXV. Alkali cleavage of aryltrimethylstannanes: an unusual electrophilic aromatic substitution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Hornfeld</surname>
<given-names>H. L.</given-names></name>
<name><surname>Walton</surname>
<given-names>D. R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1036</fpage>
<lpage>1040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Equilibria in water–ethanol mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspland</surname>
<given-names>J. R.</given-names></name>
<name><surname>Johsnon</surname>
<given-names>A.</given-names></name>
<name><surname>Peters</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1041</fpage>
<lpage>1043</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphuryl chloride as an electrophile for aromatic substitution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>R.</given-names></name>
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1044</fpage>
<lpage>1046</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Autoxidation of &lt;i&gt;N&lt;/i&gt;-alkyl amides. Part III. Mechanism of thermal oxidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sagar</surname>
<given-names>B. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1047</fpage>
<lpage>1061</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrogen-14 nuclear magnetic resonance. Part II. Additivity rules for chemical shifts in nitroalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001061</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Witanowski</surname>
<given-names>M.</given-names></name>
<name><surname>Stefaniak</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1061</fpage>
<lpage>1062</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001061">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001061">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrogen-14 nuclear magnetic resonance. Part III. A unified scale for chemical shifts in organic and aqueous solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001062</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Witanowski</surname>
<given-names>M.</given-names></name>
<name><surname>Januszewski</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1062</fpage>
<lpage>1064</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001062">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001062">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrogen-14 nuclear magnetic resonance. Part IV. Aromatic nitrocompounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001065</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Witanowski</surname>
<given-names>M.</given-names></name>
<name><surname>Stefaniak</surname>
<given-names>L.</given-names></name>
<name><surname>Webb</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1065</fpage>
<lpage>1067</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001065">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001065">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 reaction of phosphorus pentachloride and thionyl chloride with carboxylic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001067</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Green</surname>
<given-names>M.</given-names></name>
<name><surname>Thorp</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1067</fpage>
<lpage>1068</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001067">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001067">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic reactivity. Part VIII. A comparison of 1,2- and 1,4-elimination</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001069</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>R. F.</given-names></name>
<name><surname>Arendt</surname>
<given-names>J.</given-names></name>
<name><surname>Mancuso</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1069</fpage>
<lpage>1072</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001069">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001069">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance study of free radicals thermally generated from isatogen derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001072</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lunazzi</surname>
<given-names>L.</given-names></name>
<name><surname>Pedulli</surname>
<given-names>G. F.</given-names></name>
<name><surname>Maccagnasi</surname>
<given-names>G.</given-names></name>
<name><surname>Mangini</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1072</fpage>
<lpage>1076</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001072">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001072">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Correlation of reaction rates with acidity functions in strongly basic media. Part III. The effect of temperature and leaving group for aromatic &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;n&lt;/sub&gt;2 reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001076</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rochester</surname>
<given-names>C. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1076</fpage>
<lpage>1080</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001076">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001076">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Organic photochemistry. Part VI. The ultraviolet absorption spectra of &lt;i&gt;N&lt;/i&gt;-substituted hydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001081</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Conlong</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1081</fpage>
<lpage>1083</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001081">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001081">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rates of solvolysis and of base-catalysed elimination of substituted αα-dimethylphenethyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackwell</surname>
<given-names>L. F.</given-names></name>
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1084</fpage>
<lpage>1088</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part XI. Cadmium iodide–aniline equilibria in acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001088</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Satchell</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1088</fpage>
<lpage>1092</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polarisation by cation formation: a method for influencing the selectivity of radical chlorination</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001093</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kollonitsch</surname>
<given-names>J.</given-names></name>
<name><surname>Doldouras</surname>
<given-names>G. A.</given-names></name>
<name><surname>Verdi</surname>
<given-names>V. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1093</fpage>
<lpage>1095</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001093">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001093">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electric dipole moments of aniline, aminopyridines, and their &lt;i&gt;N&lt;/i&gt;-methyl derivatives in benzene and 1,4-dioxan solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Singleton</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1096</fpage>
<lpage>1099</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electric dipole moments of toluidines and some aminopicolines in benzene and 1,4-dioxan solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001100</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Singleton</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1100</fpage>
<lpage>1103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001100">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001100">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of 1,1-diaryl-2-halogenoethylenes with sodium ethoxide. Part V. Reactivity of &lt;i&gt;pp&lt;/i&gt;′-dinitro-derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001103</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beltrame</surname>
<given-names>P.</given-names></name>
<name><surname>Beltrame</surname>
<given-names>P. L.</given-names></name>
<name><surname>Sighinolfi</surname>
<given-names>O.</given-names></name>
<name><surname>Simonetta</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1103</fpage>
<lpage>1108</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001103">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001103">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic substitution by thiolate ions in some 1,1-diaryl-2-halogenoethylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001108</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beltrame</surname>
<given-names>P.</given-names></name>
<name><surname>Pitea</surname>
<given-names>D.</given-names></name>
<name><surname>Simonetta</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1108</fpage>
<lpage>1111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001108">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001108">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The diprotonation of polynuclear cinnolines in sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001112</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Altiparmakian</surname>
<given-names>R. H.</given-names></name>
<name><surname>Braithwaite</surname>
<given-names>R. S. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1112</fpage>
<lpage>1113</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Annelation and other effects in the ultraviolet absorption of polynuclear cinnolines and some analogous hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001113</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Altiparmakian</surname>
<given-names>R. H.</given-names></name>
<name><surname>Braithwaite</surname>
<given-names>R. S. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1113</fpage>
<lpage>1117</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001113">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001113">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of the adduct from &lt;i&gt;N&lt;/i&gt;-(4-bromobenzyl)isoquinolinium bromide and carbon disulphide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001117</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Newton</surname>
<given-names>M. Gary</given-names></name>
<name><surname>McDaniel</surname>
<given-names>Mildred C.</given-names></name>
<name><surname>Baldwin</surname>
<given-names>John E.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1117</fpage>
<lpage>1121</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001117">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001117">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 rapid alkaline hydrolysis of a phosphoramidothioate ester</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gerrard</surname>
<given-names>A. F.</given-names></name>
<name><surname>Hamer</surname>
<given-names>N. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1122</fpage>
<lpage>1125</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;19&lt;/sup&gt;F nuclear magnetic resonance spectra of some cyclopropane derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001125</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lee</surname>
<given-names>J.</given-names></name>
<name><surname>Parkinson</surname>
<given-names>C.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. J.</given-names></name>
<name><surname>Speight</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1125</fpage>
<lpage>1127</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001125">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001125">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Charge-transfer complexes. Part III. Solvent shifts of the charge-transfer band of complexes formed between halide ions and organic electron acceptors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>K. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1128</fpage>
<lpage>1130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Charge-transfer complexes. Part IV. Complexes of hexafluorobenzene with &lt;i&gt;n&lt;/i&gt;- and π-electron donors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001131</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaumont</surname>
<given-names>T. G.</given-names></name>
<name><surname>Davis</surname>
<given-names>K. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1131</fpage>
<lpage>1134</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of 2-chloro-1,8-phthaloylnaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001134</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Islam</surname>
<given-names>K. M. S.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1134</fpage>
<lpage>1141</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001134">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001134">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Correlation of &lt;i&gt;X&lt;/i&gt;-ray crystal structure and infrared absorption for &lt;i&gt;o&lt;/i&gt;-halogeno-aroyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001141</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eglinton</surname>
<given-names>G.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
<name><surname>Islam</surname>
<given-names>K. M. S.</given-names></name>
<name><surname>Glasby</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1141</fpage>
<lpage>1145</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001141">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001141">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies. Part II. Steric conformations of some αβ-unsaturated ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001146</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cottee</surname>
<given-names>F. H.</given-names></name>
<name><surname>Straughan</surname>
<given-names>B. P.</given-names></name>
<name><surname>Timmons</surname>
<given-names>C. J.</given-names></name>
<name><surname>Forbes</surname>
<given-names>W. F.</given-names></name>
<name><surname>Shilton</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1146</fpage>
<lpage>1151</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001146">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001146">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The formation and hydrolysis of substituted &lt;i&gt;N&lt;/i&gt;-chloro-&lt;i&gt;N&lt;/i&gt;-methylbenzamides in aqueous alkali</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001151</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hardy</surname>
<given-names>F. E.</given-names></name>
<name><surname>Robson</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1151</fpage>
<lpage>1154</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001151">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001151">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The influence of the nitro-group upon side-chain reactivity. Part IV. The inhibition of α-proton extraction from 4-nitrobenzyl chloride by the steric effect of methyl groups in the 3- and 5-positions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001154</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Doleib</surname>
<given-names>D. M.</given-names></name>
<name><surname>Iskander</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1154</fpage>
<lpage>1158</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001154">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001154">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The influence of the nitro-group upon side-chain reactivity. Part V. The rate-determining α-proton extraction from 4-nitrobenzyl chloride and 3-methyl-4-nitrobenzyl chloride in their base-catalysed interaction with their corresponding aldehydes to form epoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001159</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Doleib</surname>
<given-names>D. M.</given-names></name>
<name><surname>Iskander</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1159</fpage>
<lpage>1161</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001159">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001159">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ionisation and dissociation of some aryl fluoroaliphatic compounds under electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001162</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cotter</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1162</fpage>
<lpage>1163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001162">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001162">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aryloxy-radicals. Part VII. The electron spin resonance spectra of the secondary radicals formed during the heterogeneous oxidation of some substituted phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huysmans</surname>
<given-names>W. G. B.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1163</fpage>
<lpage>1169</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>11,11,12,12-Tetracyano-1,4-naphthaquinodimethane: a new electron acceptor</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001170</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatterjee</surname>
<given-names>Suprabhat</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1170</fpage>
<lpage>1173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001170">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001170">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ionisation of [α-&lt;sup&gt;3&lt;/sup&gt;H]acetophenone in strongly basic media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>J. R.</given-names></name>
<name><surname>Stewart</surname>
<given-names>Ross</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1173</fpage>
<lpage>1175</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some features of radical reactivity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001175</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hay</surname>
<given-names>John M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1175</fpage>
<lpage>1181</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001175">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001175">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrolysis of &lt;i&gt;gem&lt;/i&gt;-dichlorides: 2,2-dichlorobutane and 2,2-dichloropropane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001181</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Young</surname>
<given-names>B. C.</given-names></name>
<name><surname>Swinbourne</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1181</fpage>
<lpage>1184</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001181">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001181">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The preferred steric course of quaternisation of 1-alkylpiperidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001184</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. R.</given-names></name>
<name><surname>Lygo</surname>
<given-names>R.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J. M.</given-names></name>
<name><surname>Hutley</surname>
<given-names>B. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1184</fpage>
<lpage>1195</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001184">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001184">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The determination of configuration of certain quaternary salts derived from &lt;i&gt;N&lt;/i&gt;-benzyl piperidines by nuclear magnetic resonance spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001195</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. R.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1195</fpage>
<lpage>1199</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001195">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001195">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Comparative rates of nucleophilic substitution by thiophenoxide anion at axial and equatorial &lt;i&gt;N&lt;/i&gt;-alkyl groups in cyclic quaternary salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001199</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hutley</surname>
<given-names>B. G.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J.</given-names></name>
<name><surname>Stuart</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1199</fpage>
<lpage>1203</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001199">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001199">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 study of the conformational isomerisation of tetrahydropyran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001203</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gatti</surname>
<given-names>G.</given-names></name>
<name><surname>Segre</surname>
<given-names>A. L.</given-names></name>
<name><surname>Morandi</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1203</fpage>
<lpage>1204</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001203">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001203">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution of heteroaromatic compounds. Part VI. The nitration of pyridines in the 3-position as free bases and as conjugate acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001204</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ridgewell</surname>
<given-names>B. J.</given-names></name>
<name><surname>Viney</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1204</fpage>
<lpage>1210</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001204">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001204">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution of heteroaromatic compounds. Part VII. The nitration of pyridines in the α-position and rules for the nitration of substituted pyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001211</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Viney</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1211</fpage>
<lpage>1213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution of heteroaromatic compounds. Part VIII. The α-, β-, and γ-nitration of pyridine 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Shakir</surname>
<given-names>Naeem</given-names></name>
<name><surname>Viney</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1213</fpage>
<lpage>1219</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution of heteroaromatic compounds. Part IX. General form of rate profiles for acid-catalysed hydrogen exchange as illustrated by substituted aminopyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001219</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bean</surname>
<given-names>G. P.</given-names></name>
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ridgewell</surname>
<given-names>B. J.</given-names></name>
<name><surname>White</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1219</fpage>
<lpage>1222</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001219">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001219">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution of heteroaromatic compounds. Part X. Acid-catalysed hydrogen exchange at the α-, β-, and γ-positions of substituted pyridine 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001222</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bean</surname>
<given-names>G. P.</given-names></name>
<name><surname>Brignell</surname>
<given-names>P. J.</given-names></name>
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ridgewell</surname>
<given-names>B. J.</given-names></name>
<name><surname>Tarhan</surname>
<given-names>H. O.</given-names></name>
<name><surname>White</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1222</fpage>
<lpage>1226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001222">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001222">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</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 electrophilic substitution of heteroaromatic compounds. Part XI. Acid-catalysed hydrogen exchange of α- and γ-pyridones and γ-quinolone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001226</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellingham</surname>
<given-names>P.</given-names></name>
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1226</fpage>
<lpage>1233</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001226">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001226">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acidity functions and the protonation of weak bases. Part V. Second protonation of diacid bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001233</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brignell</surname>
<given-names>P. J.</given-names></name>
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Shakir</surname>
<given-names>Naeem</given-names></name>
<name><surname>Tarhan</surname>
<given-names>H. O.</given-names></name>
<name><surname>Walker</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1233</fpage>
<lpage>1235</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001233">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001233">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acidity functions and the protonation of weak bases. Part VI. The amide acidity function: its extension and application to &lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001235</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Shakir</surname>
<given-names>Naeem</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1235</fpage>
<lpage>1237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the thermal decomposition of 3-chlorobut-1-ene and 3-chloro-2-methylbut-1-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001238</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thomas</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1238</fpage>
<lpage>1241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001238">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001238">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton resonance spectra of heterocycles. Part IV. Quinoxaline and monosubstituted quinoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brignell</surname>
<given-names>P. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Reavill</surname>
<given-names>R. E.</given-names></name>
<name><surname>Cheeseman</surname>
<given-names>G. W. H.</given-names></name>
<name><surname>Sarsfield</surname>
<given-names>A. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1241</fpage>
<lpage>1243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton resonance spectra of heterocycles. Part V. 4(1&lt;i&gt;H&lt;/i&gt;)-cinnolone and substituted 4-cinnolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001243</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Lunt</surname>
<given-names>E.</given-names></name>
<name><surname>Ternai</surname>
<given-names>B.</given-names></name>
<name><surname>Tiddy</surname>
<given-names>G. J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1243</fpage>
<lpage>1248</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001243">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001243">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Applications of proton resonance spectroscopy to structural problems. Part XXVII. Phenanthrene chemistry. Part V. Configuration and conformation of some 9,9′,10,10′-tetrahydro-9,9′-biphenanthryls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001248</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>D.</given-names></name>
<name><surname>Millar</surname>
<given-names>I. T.</given-names></name>
<name><surname>Heaney</surname>
<given-names>H.</given-names></name>
<name><surname>Constantine</surname>
<given-names>P. R.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Semple</surname>
<given-names>B. M.</given-names></name>
<name><surname>Sewell</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1248</fpage>
<lpage>1250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001248">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001248">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Applications of proton resonance spectroscopy to structural problems. Part XXVIII. Orientation of 1-substituted 4- and 5-nitroimidazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001251</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>J. S. G.</given-names></name>
<name><surname>Fitzmaurice</surname>
<given-names>C.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Tiddy</surname>
<given-names>G. J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1251</fpage>
<lpage>1252</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001251">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001251">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>γ-Irradiation of maleic anhydride in benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001253</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Raciszewski</surname>
<given-names>Zbigniew</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1253</fpage>
<lpage>1258</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001253">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001253">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry of the verbenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001259</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>M. A.</given-names></name>
<name><surname>Salmon</surname>
<given-names>J. R.</given-names></name>
<name><surname>Whittaker</surname>
<given-names>D.</given-names></name>
<name><surname>Scheidegger</surname>
<given-names>U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1259</fpage>
<lpage>1261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001259">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001259">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton ionisation constants and kinetics of base hydrolysis of some α-amino-acid esters in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hay</surname>
<given-names>R. W.</given-names></name>
<name><surname>Porter</surname>
<given-names>L. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1261</fpage>
<lpage>1264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arrhenius parameters for the alkaline hydrolysis of glycine ethyl ester, in aqueous solution, and thermodynamic functions for its ionisation as an acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wright</surname>
<given-names>(Mrs.) Margaret Robson</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1265</fpage>
<lpage>1267</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Boron trifluoride–lead tetra-acetate: the oxidation of some benzenoid compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001268</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aylward</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1268</fpage>
<lpage>1270</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mass spectra of some fluorine-containing 1,2,4-oxadiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001271</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cotter</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1271</fpage>
<lpage>1272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001271">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001271">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal structure of the &lt;i&gt;p&lt;/i&gt;-bromobenzoate of a dihydro-anhydro-acetonide derivative of taxa-4(16),11-diene-5α,9α,10β,13α-tetraol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bjåmer</surname>
<given-names>Karin</given-names></name>
<name><surname>Ferguson</surname>
<given-names>George</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1272</fpage>
<lpage>1281</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fulvenes and thermochromic ethylenes. Part XLIV. Shielding effects in diphenylmethylenefluorene, fluorenylidenetriphenylphosphorane, and related substances</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001281</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovitz</surname>
<given-names>Mordecai</given-names></name>
<name><surname>Agranat</surname>
<given-names>Israel</given-names></name>
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1281</fpage>
<lpage>1284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001281">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001281">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton magnetic resonance spectra of substituted 6,7-dimethoxycinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001285</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ellis</surname>
<given-names>A. W.</given-names></name>
<name><surname>Lovesey</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1285</fpage>
<lpage>1287</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001285">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001285">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanistic studies in strongly basic media. Part V. Kinetics and mechanism of bifluorenylidene formation from 2-substituted 9-halogenofluorenes in t-butyl alcohol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001287</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bethell</surname>
<given-names>D.</given-names></name>
<name><surname>Cockerill</surname>
<given-names>A. F.</given-names></name>
<name><surname>Frankham</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1287</fpage>
<lpage>1294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001287">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001287">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. Carbon–carbon bond polarisabilities in relation to bond lengths</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001295</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radom</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1295</fpage>
<lpage>1298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001295">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001295">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electron spin resonance of some dialkyl nitroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001299</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>A.</given-names></name>
<name><surname>Hussain</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1299</fpage>
<lpage>1300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001299">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001299">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rate correlations involving the linear combination of substituent parameters. Part III. Reactions of picryl chloride with substituted phenoxide ions and anilines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001300</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ryan</surname>
<given-names>J. J.</given-names></name>
<name><surname>Humffray</surname>
<given-names>A. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1300</fpage>
<lpage>1305</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001300">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001300">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of the benzil monoximes: &lt;i&gt;X&lt;/i&gt;-ray analysis of benzil α-monoxime &lt;i&gt;p&lt;/i&gt;-bromobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kerr</surname>
<given-names>K. Ann</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1305</fpage>
<lpage>1310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An &lt;i&gt;X&lt;/i&gt;-ray study of the &lt;i&gt;p&lt;/i&gt;-n-alkoxybenzoic acids. Part II. The crystal structure of anisic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryan</surname>
<given-names>Robert F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1311</fpage>
<lpage>1316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of 2-chlorobicyclo[3,3,1]nonan-9-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Webb</surname>
<given-names>N. C.</given-names></name>
<name><surname>Becker</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1317</fpage>
<lpage>1321</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic assistance in the cyclisation of aldose acetals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001322</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>Brian</given-names></name>
<name><surname>Thacker</surname>
<given-names>David</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1322</fpage>
<lpage>1326</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001322">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001322">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Non-electrolyte effects upon rates of nitration in anhydrous sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001326</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akand</surname>
<given-names>M. A.</given-names></name>
<name><surname>Wyatt</surname>
<given-names>P. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1326</fpage>
<lpage>1329</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001326">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001326">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XIII. The oxidation of mesoinositol and some monosaccharides by the hydroxy-radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Pritchett</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1329</fpage>
<lpage>1332</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Changes in weak-base p&lt;i&gt;K&lt;/i&gt;&lt;sub&gt;BH&lt;sup&gt;+&lt;/sup&gt;&lt;/sub&gt; values upon excitation to the first excited singlet state</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001333</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hopkinson</surname>
<given-names>A. C.</given-names></name>
<name><surname>Wyatt</surname>
<given-names>P. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1333</fpage>
<lpage>1335</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001333">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001333">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The carbonyl group frequency. Part I. Aliphatic ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001336</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morgan</surname>
<given-names>K. J.</given-names></name>
<name><surname>Unwin</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1336</fpage>
<lpage>1340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001336">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001336">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A spectroscopic study of complex formation between aromatic nitrocompounds and sodium sulphite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001341</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1341</fpage>
<lpage>1346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001341">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001341">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The complete conversion of the highly hindered ester, 2-carbamoylphenyl mesitoate, into the highly hindered amide, mesitamide, via base-catalysed intramolecular nucleophilic amide-group participation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Topping</surname>
<given-names>R. Malcolm</given-names></name>
<name><surname>Tutt</surname>
<given-names>David E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1346</fpage>
<lpage>1350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvation evidence for the lifetime of donor–acceptor complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Isaacs</surname>
<given-names>Neil S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1351</fpage>
<lpage>1352</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the autoxidation of toluenes catalysed by cobaltic acetate. Part II. Effects of benzaldehyde, cobalt, and substituent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001353</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morimoto</surname>
<given-names>T.</given-names></name>
<name><surname>Ogata</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1353</fpage>
<lpage>1357</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001353">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001353">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics of the reactions of silicon compounds. Part II. The gas-phase thermal decomposition of 3,3,3-trifluoropropyltrifluorosilane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001357</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. J.</given-names></name>
<name><surname>Simmons</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1357</fpage>
<lpage>1361</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001357">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001357">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substitution in polymethylbenzenes. Part XXIII. Arrhenius parameters for the chlorination of polymethylbenzenes in 1 : 1 acetic acid–propionic acid mixture</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001361</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baciocchi</surname>
<given-names>Enrico</given-names></name>
<name><surname>Mandolini</surname>
<given-names>Luigi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1361</fpage>
<lpage>1363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001361">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001361">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A vibrational assignment for pyrazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001363</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zecchina</surname>
<given-names>A.</given-names></name>
<name><surname>Cerruti</surname>
<given-names>L.</given-names></name>
<name><surname>Coluccia</surname>
<given-names>S.</given-names></name>
<name><surname>Borello</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1363</fpage>
<lpage>1368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001363">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001363">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structure and chemistry of the perchlorate of anhydro-&lt;i&gt;N&lt;/i&gt;-hydroxymethyldeoxyangustifoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birnbaum</surname>
<given-names>G. I.</given-names></name>
<name><surname>Cheung</surname>
<given-names>K. K.</given-names></name>
<name><surname>Wiewiorowski</surname>
<given-names>M.</given-names></name>
<name><surname>Bratek-Wiewiorowska</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1368</fpage>
<lpage>1374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001368">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of a compound, C&lt;sub&gt;20&lt;/sub&gt;H&lt;sub&gt;33&lt;/sub&gt;N&lt;sub&gt;3&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chieh</surname>
<given-names>P. C.</given-names></name>
<name><surname>Trotter</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1375</fpage>
<lpage>1380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calculated and observed oxidising capacities of manganese oxides in the oxidation of cinnamyl alcohol in neutral solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dollimore</surname>
<given-names>D.</given-names></name>
<name><surname>Tonge</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1380</fpage>
<lpage>1384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of tribenzyloxyaluminium and some related alkoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Barnard</surname>
<given-names>Mary</given-names></name>
<name><surname>Chambers</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1385</fpage>
<lpage>1389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal decomposition of tribenzyloxyaluminium and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001389</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayres</surname>
<given-names>D. C.</given-names></name>
<name><surname>Chambers</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1389</fpage>
<lpage>1392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001389">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001389">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Index of authors, 1967</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001393</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1393</fpage>
<lpage>1404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001393">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001393">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Index of subjects, 1967</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29670001405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>1405</fpage>
<lpage>1418</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29670001405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J29670001405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Errata</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2967000X001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1967</year></pub-date>
<volume>1967</volume>
<issue />
<fpage>X001</fpage>
<lpage>X001</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2967000X001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1967/J2/J2967000X001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
</articles>
