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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/J297100FP001</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J297100FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J297100FP001">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/J297100FP003</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J297100FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J297100FP003">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>Kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XXII. The nitration of pyrimidinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000001</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>Kingsland</surname>
<given-names>M.</given-names></name>
<name><surname>Scriven</surname>
<given-names>E. F. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1</fpage>
<lpage>4</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 electrophilic substitution of heteroaromatic compounds. Part XXIII. Acid-catalysed hydrogen exchange of quinoline, isoquinoline, and their &lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bressel</surname>
<given-names>U.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Lea</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>4</fpage>
<lpage>10</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 electrophilic substitution of heteroaromatic compounds. Part XXIV. Acid-catalysed hydrogen exchange of 2-naphthol and of some corresponding aza-, thia-, and oxo-derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bressel</surname>
<given-names>U.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Lea</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>11</fpage>
<lpage>18</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 substitutions in carbonic acid derivatives. Part I. Kinetics and mechanisms of the reaction of ethyl chloroformate with substituted anilines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ostrogovich</surname>
<given-names>G.</given-names></name>
<name><surname>Csunderlik</surname>
<given-names>C.</given-names></name>
<name><surname>Bacaloglu</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>18</fpage>
<lpage>22</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intermediates in the decomposition of aliphatic diazo-compounds. Part VIII. The mechanism of ether formation from diarylmethylenes and alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000023</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bethell</surname>
<given-names>D.</given-names></name>
<name><surname>Newall</surname>
<given-names>A. R.</given-names></name>
<name><surname>Whittaker</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>23</fpage>
<lpage>31</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000023">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000023">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydrogen isotope exchange reactions. Part XXI. Heterolytic tritium exchange between resorcinol and water in the homogeneous liquid phase</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000032</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Lee</surname>
<given-names>J. R.</given-names></name>
<name><surname>Gitter</surname>
<given-names>(Miss) A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>32</fpage>
<lpage>40</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000032">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000032">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hammett acidity functions (&lt;i&gt;H&lt;/i&gt;&lt;sub&gt;–&lt;/sub&gt;) of lithium, sodium, and potassium glycoxide solutions in ethylene glycol at 25 °C</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kundu</surname>
<given-names>K. K.</given-names></name>
<name><surname>Aiyar</surname>
<given-names>Lakshmi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>40</fpage>
<lpage>44</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 role of the α-effect in determining nucleophilic reactivities: aromatic substitutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biggi</surname>
<given-names>Gino</given-names></name>
<name><surname>Pietra</surname>
<given-names>Francesco</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>44</fpage>
<lpage>48</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Wavelength effect in the photolysis of halogenated ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000048</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Majer</surname>
<given-names>J. R.</given-names></name>
<name><surname>Olavesen</surname>
<given-names>C.</given-names></name>
<name><surname>Robb</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>48</fpage>
<lpage>55</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid-catalysed alcoholysis of epoxides. Part I. Reactions of substituted (1,2-epoxyethyl)benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000055</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biggs</surname>
<given-names>J.</given-names></name>
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Finch</surname>
<given-names>A. F.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>55</fpage>
<lpage>63</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000055">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000055">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid-catalysed alcoholysis of epoxides. Part II. Methanolysis of 1,1-diphenylethylene oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000063</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biggs</surname>
<given-names>J.</given-names></name>
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>63</fpage>
<lpage>65</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000063">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000063">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid-catalysed alcoholysis of epoxides. Part III. Alcoholysis of 1,2-epoxypropane, 1,2-epoxy-3-phenoxypropane, 1,2-epoxy-3-phenylpropane, and 2,3-epoxypropan-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000066</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biggs</surname>
<given-names>J.</given-names></name>
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>66</fpage>
<lpage>71</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000066">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000066">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid-catalysed alcoholysis of epoxides. Part IV. Methanolysis of D(+)-(1,2-epoxyethyl)benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000071</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biggs</surname>
<given-names>J.</given-names></name>
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>71</fpage>
<lpage>74</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000071">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000071">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 sulphones. Part X. Kinetic evidence for the aromatic character of anions derived from benzo- and dibenzothiopyran &lt;i&gt;SS&lt;/i&gt;-dioxide systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradamante</surname>
<given-names>(Mrs.) S.</given-names></name>
<name><surname>Maiorana</surname>
<given-names>S.</given-names></name>
<name><surname>Mangia</surname>
<given-names>A.</given-names></name>
<name><surname>Pagani</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>74</fpage>
<lpage>78</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 substitutions in five-membered heteroaromatic systems. Part XII. A quantitative study on the reactivities of the α- and β-positions of benzofuran and benzothiophen in electrophilic substitutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000079</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clementi</surname>
<given-names>S.</given-names></name>
<name><surname>Linda</surname>
<given-names>P.</given-names></name>
<name><surname>Marino</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>79</fpage>
<lpage>82</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000079">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000079">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 as solutes of 9,10-dihydroanthracene, anthrone, and xanthone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000082</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Cleaver</surname>
<given-names>(Mrs.) Georgina</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Pierens</surname>
<given-names>R. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>82</fpage>
<lpage>85</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000082">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000082">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Bromohydrin formation in aqueous dimethyl sulphoxide; electronic and steric effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000085</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dalton</surname>
<given-names>David R.</given-names></name>
<name><surname>Dutta</surname>
<given-names>Ved P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>85</fpage>
<lpage>89</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000085">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000085">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXIX. Chlorination of aromatic hydrocarbons in slightly aqueous (96%) dioxan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Main</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>90</fpage>
<lpage>94</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free-radical addition to olefins. Part VII. Addition of trichloromethyl radicals to chloro-olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000095</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johari</surname>
<given-names>D. P.</given-names></name>
<name><surname>Sidebottom</surname>
<given-names>H. W.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
<name><surname>Walton</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>95</fpage>
<lpage>99</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000095">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000095">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 steroids in sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>Howard A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>99</fpage>
<lpage>101</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 substitution on the thiophen ring. Part IV. Kinetics and mechanism of the nitration of thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000102</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>Anthony R.</given-names></name>
<name><surname>Hendry</surname>
<given-names>James B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>102</fpage>
<lpage>105</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000102">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000102">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Differential gas–liquid chromatographic behaviour in diastereoisomeric systems. Part I. Symmetrically substituted dichiral hydrocarbons and ester precursors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000106</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feibush</surname>
<given-names>Binyamin</given-names></name>
<name><surname>Spialter</surname>
<given-names>Leonard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>106</fpage>
<lpage>110</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000106">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000106">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Differential gas–liquid chromatographic behaviour in diastereoisomeric systems. Part II. Assignment of diastereomer configuration in 2,3-dipentylbutanes and 2,4-dipentylpentanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000111</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feibush</surname>
<given-names>Binyamin</given-names></name>
<name><surname>Spialter</surname>
<given-names>Leonard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>111</fpage>
<lpage>115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000111">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000111">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Differential gas–liquid chromatographic behaviour in diastereoisomeric systems. Part III. Symmetrically substituted dichiral ethers, alkoxysiloxanes, and disiloxanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feibush</surname>
<given-names>Binyamin</given-names></name>
<name><surname>Spialter</surname>
<given-names>Leonard</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>115</fpage>
<lpage>117</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;cis&lt;/i&gt;-2,2,3,4,4-pentamethyl-1-phenylphosphetan 1-oxide, C&lt;sub&gt;14&lt;/sub&gt;H&lt;sub&gt;21&lt;/sub&gt;PO</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000117</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>117</fpage>
<lpage>120</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000117">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000117">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 dipole moments and molar Kerr constants of benzaldehyde, acetophenone, 1,4-diformylbenzene, and 1,4-diacetylbenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000120</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>P. 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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>120</fpage>
<lpage>123</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000120">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000120">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid-catalysed hydrolysis and protonation behaviour of hydroxamic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000123</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buglass</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hudson</surname>
<given-names>K.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>123</fpage>
<lpage>126</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000123">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000123">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 base cleavage of X·C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;·[CC]&lt;sub&gt;&lt;i&gt;n&lt;/i&gt;&lt;/sub&gt;·MEt&lt;sub&gt;3&lt;/sub&gt; compounds (&lt;i&gt;n&lt;/i&gt;= 2 and 3, M = Si and Ge), and their significance for theories of substituent effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000127</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Eastmond</surname>
<given-names>R.</given-names></name>
<name><surname>Walton</surname>
<given-names>D. R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>127</fpage>
<lpage>130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000127">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000127">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXVI. The alkaline ferricyanide oxidation of pyridinium salts. Effects of substituents and mechanism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000131</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Vinutha</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>131</fpage>
<lpage>136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 theoretical study of the Edward–Lemieux effect (the anomeric effect). The stereochemical requirements of adjacent electron pairs and polar bonds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wolfe</surname>
<given-names>Saul</given-names></name>
<name><surname>Rauk</surname>
<given-names>Arvi</given-names></name>
<name><surname>Tel</surname>
<given-names>Luis M.</given-names></name>
<name><surname>Csizmadia</surname>
<given-names>I. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>136</fpage>
<lpage>145</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbonyl compounds in basic solutions. Part II. The mechanism of the alkaline hydrolysis of methyl 2-benzoylbenzoates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000145</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>145</fpage>
<lpage>148</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000145">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000145">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbonyl compounds in basic solutions. Part III. The mechanism of the alkaline hydrolysis of methyl 2-aroyl- and 2-acylbenzoates and related esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000149</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>149</fpage>
<lpage>156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000149">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000149">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbonyl compounds in basic solutions. Part IV. The mechanism of the alkaline hydrolysis of methyl 3-benzoylacrylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Henry</surname>
<given-names>M. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>156</fpage>
<lpage>160</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transmission of polar effects. Part XIII. The polar effects of &lt;i&gt;para&lt;/i&gt;-acyl and -aroyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000161</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Shaw</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>161</fpage>
<lpage>162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000161">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000161">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrochemical reduction of aromatic thiocarbonyls to the corresponding radical anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000162</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lunazzi</surname>
<given-names>L.</given-names></name>
<name><surname>Maccagnani</surname>
<given-names>G.</given-names></name>
<name><surname>Mazzanti</surname>
<given-names>G.</given-names></name>
<name><surname>Placucci</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>162</fpage>
<lpage>166</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000162">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000162">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;anti&lt;/i&gt;-3′,4′-difluoro-2-hydroxyiminopropiophenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000166</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>F. H.</given-names></name>
<name><surname>Trotter</surname>
<given-names>James</given-names></name>
<name><surname>Rogers</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>166</fpage>
<lpage>171</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000166">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000166">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sensitivity to the activating group in &lt;i&gt;E&lt;/i&gt;1&lt;i&gt;CB&lt;/i&gt; eliminations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000171</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>171</fpage>
<lpage>173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ultraviolet spectra of aqueous alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrett</surname>
<given-names>Jack</given-names></name>
<name><surname>Mansell</surname>
<given-names>A. L.</given-names></name>
<name><surname>Fox</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>173</fpage>
<lpage>174</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 VII. The addition of 2,4-dinitrobenzenesulphenyl chloride to aliphatic alkenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000175</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beverly</surname>
<given-names>G. M.</given-names></name>
<name><surname>Hogg</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>175</fpage>
<lpage>177</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000175">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000175">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Skeletal rearrangements of siliconium ions in the gas phase: mass spectra of some phenoxasilins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000177</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lengyel</surname>
<given-names>I.</given-names></name>
<name><surname>Aaronson</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>177</fpage>
<lpage>181</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000177">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000177">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 autoxidation of triethylborane. Part II. Importance of an autocatalytic initiation reaction in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grotewold</surname>
<given-names>J.</given-names></name>
<name><surname>Hernandez</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>182</fpage>
<lpage>185</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reaction of the bis(dimethylglyoximinato)-pyridinecobalt(I) anion with &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-β-bromostyrenes and with phenylacetylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000185</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Meeks</surname>
<given-names>B. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>185</fpage>
<lpage>189</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000185">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000185">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXVIII. Oxidation of enols, enol ethers, and related compounds with the hydroxyl and the amino-radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000189</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edge</surname>
<given-names>D. J.</given-names></name>
<name><surname>Gilbert</surname>
<given-names>B. C.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>West</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>189</fpage>
<lpage>196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000189">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000189">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of olefins. Part XI. Reaction of &lt;i&gt;p&lt;/i&gt;-substituted dideuteriostyrenes with benzene in the presence of palladium(II) acetate: a mechanistic study</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000196</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Danno</surname>
<given-names>S.</given-names></name>
<name><surname>Moritani</surname>
<given-names>I.</given-names></name>
<name><surname>Fujiwara</surname>
<given-names>Y.</given-names></name>
<name><surname>Teranishi</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>196</fpage>
<lpage>198</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000196">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000196">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XI. &lt;i&gt;X&lt;/i&gt;-ray determination of the structure of vernolepin &lt;i&gt;p&lt;/i&gt;-bromobenzenesulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000198</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McPhail</surname>
<given-names>A. T.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>198</fpage>
<lpage>202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000198">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000198">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 alkaline hydrolysis of alkyl esters of anthraquinone-1- and -2-carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Rahim</surname>
<given-names>A.</given-names></name>
<name><surname>Waters</surname>
<given-names>D. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>202</fpage>
<lpage>204</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part IX. Synthesis, structure, and spectra of acyclic dienamines; linear &lt;i&gt;versus&lt;/i&gt; cross-conjugation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000205</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>B. J.</given-names></name>
<name><surname>Yoxall</surname>
<given-names>C. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>205</fpage>
<lpage>212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000205">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000205">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the reaction of cyclopentadienylidenetriarylphosphoranes with cyano-olefins. Part II. Nucleophilic addition to benzylidenemalononitriles; a linear free energy relationship between rate and equilibrium constant for π-complex formation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lord</surname>
<given-names>E.</given-names></name>
<name><surname>Naan</surname>
<given-names>M. P.</given-names></name>
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>213</fpage>
<lpage>219</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the reaction of cyclopentadienylidenetriarylphosphoranes with cyano-olefins. Part III. Elimination of hydrogen cyanide from 2-(1-phenyl-1,2,2-tricyanoethyl)cyclopentadienylidenetriphenylphosphorane; an &lt;i&gt;E&lt;/i&gt;1&lt;i&gt;CB&lt;/i&gt; reaction &lt;i&gt;via&lt;/i&gt; an ion-pair</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000220</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lord</surname>
<given-names>E.</given-names></name>
<name><surname>Naan</surname>
<given-names>M. P.</given-names></name>
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>220</fpage>
<lpage>224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000220">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000220">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 heteroaromatic substitution. Part XXXIV. Fluorine &lt;i&gt;versus&lt;/i&gt; chlorine mobility in reactions with methanolic methoxide ion and with piperidine in various solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bressan</surname>
<given-names>G. B.</given-names></name>
<name><surname>Giardi</surname>
<given-names>I.</given-names></name>
<name><surname>Illuminati</surname>
<given-names>G.</given-names></name>
<name><surname>Linda</surname>
<given-names>P.</given-names></name>
<name><surname>Sleiter</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>225</fpage>
<lpage>230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Application of the additivity of shielding effects in olefinic compounds for configurational assignments to isomeric 4-amino-1,2-diarylbut-2-enes possessing antihistaminic activity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ison</surname>
<given-names>R. R.</given-names></name>
<name><surname>Casy</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>230</fpage>
<lpage>233</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part XXXV. The thermal decomposition of benzoyl peroxide in aromatic solvents in the presence of nitrobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000233</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chalfont</surname>
<given-names>G. R.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Liang</surname>
<given-names>K. S. Y.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>233</fpage>
<lpage>245</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000233">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000233">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidation of diphenylhydroxylamine by benzoyl peroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000245</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chalfont</surname>
<given-names>G. R.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>245</fpage>
<lpage>249</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Investigation of possible isomerisation reactions in benzene, iodobenzene, and phenol upon electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000249</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dickinson</surname>
<given-names>R. J.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>249</fpage>
<lpage>251</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Type 2 photoelimination reaction of esters of aromatic carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000251</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Coyle</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>251</fpage>
<lpage>255</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000251">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000251">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Measurement of electrophilic aromatic reactivities &lt;i&gt;via&lt;/i&gt; pyrolysis of 1-arylethyl acetates. Part IV. The deactivating effect of the pentafluorophenyl group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000255</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>255</fpage>
<lpage>257</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000255">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000255">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;X&lt;/i&gt;-ray studies of terpenoid derivatives. Part II. Crystal and molecular structure of the 1 :1 adduct of germacratriene with silver nitrate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000257</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>F. H.</given-names></name>
<name><surname>Rogers</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>257</fpage>
<lpage>262</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000257">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000257">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of mass spectra of organic compounds. Part VIII. Calculation of ionization potentials of disubstituted benzenes and their importance in Hammett correlations in mass spectrometry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000263</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>T. W.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>263</fpage>
<lpage>268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000263">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000263">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 eliminations. Part XIII. The pyrolysis of 1,1- and 1,2-dibromoethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000268</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Good</surname>
<given-names>P. T.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>268</fpage>
<lpage>272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000268">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000268">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of triphenylsilyl halides with sodium naphthalenide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fearon</surname>
<given-names>F. W. G.</given-names></name>
<name><surname>Young</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>272</fpage>
<lpage>276</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ambident neighbouring groups. Part V. Effects of solvent on several O-5 ring closures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000277</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Flynn</surname>
<given-names>E. J.</given-names></name>
<name><surname>Fenton</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>277</fpage>
<lpage>278</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000277">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000277">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridone–pyridol tautomerism in 2-hydroxypyridines with [5,6]-annelated rings and oxygen at the [6]-position: 2,3-dihydro-6-hydroxy-4-methylfuro[2,3-&lt;i&gt;b&lt;/i&gt;]pyridine and 3,4-dihydro-7-hydroxy-5-methylpyrano-[2,3-&lt;i&gt;b&lt;/i&gt;]pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000279</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
<name><surname>Yeoh</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>279</fpage>
<lpage>289</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000279">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000279">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyridone–pyridol tautomerism in 2-hydroxypyridines with [5,6]-annelated rings and carbon atoms at positions [5] and [6] : 1,3-dihydro-5-hydroxyfuro[3,4-&lt;i&gt;b&lt;/i&gt;]pyridine, 1,3-dihydro-5-hydroxythieno[3,4-&lt;i&gt;b&lt;/i&gt;]pyridine, and 1,3-dihydro-5-hydroxythieno[3,4-&lt;i&gt;b&lt;/i&gt;]pyridine &lt;i&gt;S&lt;/i&gt;,&lt;i&gt;S&lt;/i&gt;-dioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000289</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
<name><surname>Yeoh</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>289</fpage>
<lpage>296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000289">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000289">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effect of unsaturated electron-withdrawing substituents on the tautomerism of 2-hydroxypyridines: 6-hydroxy-2,3-bis(methoxycarbonyl)-pyridine and 5-cyano-2,3-dihydro-6-hydroxy-4-methylfuro[2,3-&lt;i&gt;b&lt;/i&gt;]pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000296</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
<name><surname>Yeoh</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>296</fpage>
<lpage>298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000296">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000296">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 at saturated carbon. Part VIII. Solvent effects on the free energy of trimethylamine, the nitrobenzyl chlorides, and the trimethylamine–nitrobenzyl chloride transition states</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000299</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>299</fpage>
<lpage>308</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000299">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000299">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Phenyl ring–substituent interactions in substituted acetanilides. Part II. Infrared spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000309</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bennett</surname>
<given-names>J.</given-names></name>
<name><surname>Maire</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>309</fpage>
<lpage>311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000309">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000309">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 importance of &lt;i&gt;d&lt;/i&gt;-orbitals in determining the ultraviolet spectra of cyclic organic sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000312</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>D. R.</given-names></name>
<name><surname>Kontnik</surname>
<given-names>L. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>312</fpage>
<lpage>315</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000312">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000312">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 IX. The radical anion of 1-phenyl-2-trimethylsilylacetylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000315</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>Emes</surname>
<given-names>P. J.</given-names></name>
<name><surname>Phelan</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>315</fpage>
<lpage>318</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000315">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000315">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 effects in di- and tri-arylmethane dyes. Part X. Electronic absorption spectra of bridged derivatives of malachite green and crystal violet</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000319</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aaron</surname>
<given-names>C.</given-names></name>
<name><surname>Barker</surname>
<given-names>C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>319</fpage>
<lpage>324</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000319">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000319">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aspects of the Strecker aminonitrile synthesis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000325</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ogata</surname>
<given-names>Y.</given-names></name>
<name><surname>Kawasaki</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>325</fpage>
<lpage>329</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000325">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000325">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 resonance study of Schlenk's hydrocarbon</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Luckhurst</surname>
<given-names>G. R.</given-names></name>
<name><surname>Pedulli</surname>
<given-names>G. F.</given-names></name>
<name><surname>Tiecco</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>329</fpage>
<lpage>334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nuclear magnetic resonance chemical shifts caused by protonation. Part II. Formamide and some &lt;i&gt;N&lt;/i&gt;-alkyl and &lt;i&gt;NN&lt;/i&gt;-dialkyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Liler</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>334</fpage>
<lpage>338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 apparent conformations of acetic anhydride and diacetyl sulphide as solutes in benzene or carbon tetrachloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000338</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hopkins</surname>
<given-names>P. A.</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>338</fpage>
<lpage>341</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000338">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000338">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 spectrometry of quinones. Part II. A study of the distinguishing features found in the mass spectra of 1,2- and 1,4-naphthaquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000341</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oliver</surname>
<given-names>R. W. A.</given-names></name>
<name><surname>Rashman</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>341</fpage>
<lpage>344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000341">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000341">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 studies by nuclear magnetic resonance. Part I. The barrier to hindered rotation in 4-dimethylaminobut-3-en-2-one around the C–C single bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000345</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dabrowski</surname>
<given-names>J.</given-names></name>
<name><surname>Kozerski</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>345</fpage>
<lpage>348</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000345">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000345">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 data from equilibrium studies of the nitric oxide-catalysed isomerization of 1,3,5-heptatriene in the gas phase</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000348</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Egger</surname>
<given-names>Kurt W.</given-names></name>
<name><surname>James</surname>
<given-names>Thomas Ll.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>348</fpage>
<lpage>350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000348">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000348">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enamine chemistry. Part X. Ultraviolet absorption spectra of dienamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Firrell</surname>
<given-names>N. F.</given-names></name>
<name><surname>Hickmott</surname>
<given-names>P. W.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>351</fpage>
<lpage>353</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of spiradine A: &lt;i&gt;X&lt;/i&gt;-ray analysis of spiradine A methiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000354</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sasaki</surname>
<given-names>Kyoyu</given-names></name>
<name><surname>Sakabe</surname>
<given-names>Noriyoshi</given-names></name>
<name><surname>Hirata</surname>
<given-names>Yoshimasa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>354</fpage>
<lpage>356</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000354">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000354">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 examination of some fluorescent derivatives of 2,2′-bithienyl and 2-(2′-furyl)-thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000357</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. E.</given-names></name>
<name><surname>Hardy</surname>
<given-names>F. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>357</fpage>
<lpage>361</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000357">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000357">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 gas-phase reactions of ethylidenecyclobutane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000362</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>M. C.</given-names></name>
<name><surname>Gibbons</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>362</fpage>
<lpage>364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000362">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000362">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tracer studies on the reductive coupling of 1-Naphthyldiazonium ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000365</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Thomas</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>365</fpage>
<lpage>366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000365">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000365">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 novel approach to the determination of activation energies by nuclear magnetic spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000366</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marquardt</surname>
<given-names>Fritz-Hans</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>366</fpage>
<lpage>368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000366">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000366">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 1,2,3-benzothiadiazoles. Part II. The nuclear magnetic resonance spectra of the nitro-, bromo-, and methoxy-1,2,3-benzothiadiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Poesche</surname>
<given-names>W. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>368</fpage>
<lpage>373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000368">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of vinyl sulphonic esters. Part IV. Evidence of an &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;1-type mechanism involving an ethylenic carbon atom</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000374</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Tonellato</surname>
<given-names>U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>374</fpage>
<lpage>380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000374">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000374">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of vinyl sulphonic esters. Part V. Stereochemistry and rearrangements in &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;1 reactions of β-thiovinyl trinitrobenzenesulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000381</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Tonellato</surname>
<given-names>U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>381</fpage>
<lpage>385</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000381">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000381">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 dipolar contribution to the ground state in a series of fulvenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pines</surname>
<given-names>Alexander</given-names></name>
<name><surname>Rabinovitz</surname>
<given-names>Mordecai</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>385</fpage>
<lpage>388</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 proton magnetic resonance spectra of fluorene and its derivatives. Part III. 9-Substituted fluorenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000388</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartle</surname>
<given-names>K. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. W.</given-names></name>
<name><surname>Bavin</surname>
<given-names>P. M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>388</fpage>
<lpage>396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000388">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000388">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 chemical shifts in some substituted anilines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hampson</surname>
<given-names>P.</given-names></name>
<name><surname>Mathias</surname>
<given-names>A.</given-names></name>
<name><surname>Westhead</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>397</fpage>
<lpage>399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 parameters and aromatic systems. Part II. Detritiation of substituted fluoranthenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000400</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bancroft</surname>
<given-names>K. C. C.</given-names></name>
<name><surname>Howe</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>400</fpage>
<lpage>403</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000400">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000400">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 spectrum of the 2,4,5-triphenylimidazolyl radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cyr</surname>
<given-names>Natsuko</given-names></name>
<name><surname>Wilks</surname>
<given-names>M. A. J.</given-names></name>
<name><surname>Willis</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>404</fpage>
<lpage>406</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 amides, esters, and related compounds in acid solution. Part III. Ureas</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000407</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Farlow</surname>
<given-names>D. W.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>407</fpage>
<lpage>410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000407">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000407">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of pancuronium bromide (3α,17β-diacetoxy-2β,16β-dipiperidino-5α-androstane dimethobromide), a neuromuscular blocking agent. Crystal and molecular structure of the water: methylene chloride solvate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Savage</surname>
<given-names>D. S.</given-names></name>
<name><surname>Cameron</surname>
<given-names>A. F.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
<name><surname>Hannaway</surname>
<given-names>C.</given-names></name>
<name><surname>Mackay</surname>
<given-names>I. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>410</fpage>
<lpage>415</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 diphenylhydrazone of 1,2,4-trithiolane-3,5-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000415</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casalone</surname>
<given-names>G.</given-names></name>
<name><surname>Mugnoli</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>415</fpage>
<lpage>418</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000415">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000415">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 proton magnetic resonance study of π-cycloheptadienyl complexes of manganese tricarbonyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000418</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foreman</surname>
<given-names>M. I.</given-names></name>
<name><surname>Haque</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>418</fpage>
<lpage>421</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000418">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000418">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electric dipole moments and molecular conformations of aromatic amines, phosphites, and phosphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000422</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Thurston</surname>
<given-names>A. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>422</fpage>
<lpage>426</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000422">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000422">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Lanthanide ions as sensitive probes. Part IV. Transfer of triplet energy from 2-acetylfluorene and 2-acetonaphthone to tervalent terbium in a rigid matrix</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000427</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mushrush</surname>
<given-names>George W.</given-names></name>
<name><surname>Minn</surname>
<given-names>Fredrick L.</given-names></name>
<name><surname>Filipescu</surname>
<given-names>Nicolae</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>427</fpage>
<lpage>430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000427">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000427">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydroxylation. Part V. Photoinduced oxidation of some benzenoid compounds by trialkyl phosphite esters and oxygen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000430</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Higgins</surname>
<given-names>R.</given-names></name>
<name><surname>Kitson</surname>
<given-names>K. M.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. R. Lindsay</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>430</fpage>
<lpage>435</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000430">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000430">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Aromatic isothiocyanates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000435</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheng</surname>
<given-names>C. L.</given-names></name>
<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>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>435</fpage>
<lpage>437</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000435">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000435">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 studies on 1,3-dioxepans. Part III. 2,5-&lt;i&gt;O&lt;/i&gt;-methylene-D-mannitol and some related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000437</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stoddart</surname>
<given-names>J. F.</given-names></name>
<name><surname>Szarek</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>437</fpage>
<lpage>442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000437">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000437">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of a complex between silver iodide and piperidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>Gerald B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>443</fpage>
<lpage>446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 n.m.r. spectra and conformations of cyclic compounds part V. Mechanism of CH·CH coupling in heterocyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
<name><surname>Parry</surname>
<given-names>K.</given-names></name>
<name><surname>Thomas</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>446</fpage>
<lpage>453</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acyl sulphonate reactions. Part II. Solvolyses of a series of 4- and 5-substituted 2-sulphobenzoic anhydrides in hydroxylic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laird</surname>
<given-names>R. M.</given-names></name>
<name><surname>Spence</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>454</fpage>
<lpage>456</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;ortho&lt;/i&gt;-effect in 2-amino- and 2-methylamino-benzylidyne trifluoride, (2-trifluoromethyl- and 2-trifluoromethyl-&lt;i&gt;N&lt;/i&gt;-methyl-aniline)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000457</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grocock</surname>
<given-names>D. E.</given-names></name>
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
<name><surname>Hepworth</surname>
<given-names>J. D.</given-names></name>
<name><surname>Hudson</surname>
<given-names>J. A.</given-names></name>
<name><surname>Ibbitson</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>457</fpage>
<lpage>459</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000457">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000457">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 correlation of solvent effects on physical and chemical properties</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000460</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fowler</surname>
<given-names>F. W.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Rutherford</surname>
<given-names>R. J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>460</fpage>
<lpage>469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000460">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000460">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polysaccharide conformation. Part VI. Computer model-building for linear and branched pyranoglycans. Correlations with biological function. Preliminary assessment of inter-residue forces in aqueous solution. Further interpretation of optical rotation in terms of chain conformation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rees</surname>
<given-names>D. A.</given-names></name>
<name><surname>Scott</surname>
<given-names>W. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>469</fpage>
<lpage>479</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 investigation of the 4,5-methylenephenanthrene dianion radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000479</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casson</surname>
<given-names>D.</given-names></name>
<name><surname>Tabner</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>479</fpage>
<lpage>482</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000479">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000479">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the perchloric acid-catalysed hydrolyses of &lt;i&gt;para&lt;/i&gt;-substituted benzoic anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000483</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calvaruso</surname>
<given-names>G.</given-names></name>
<name><surname>Cavasino</surname>
<given-names>F. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>483</fpage>
<lpage>491</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000483">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000483">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 electron spin resonance spectroscopy. Part I. The photoreduction of biacetyl and pyruvic acid in organic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000491</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayscough</surname>
<given-names>P. B.</given-names></name>
<name><surname>Brice</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>491</fpage>
<lpage>498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000491">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000491">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Part III. Rate coefficients for elimination from substituted 2-phenylethyl arenesulphonates with potassium in t-butyl alcohol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000498</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banger</surname>
<given-names>J.</given-names></name>
<name><surname>Cockerill</surname>
<given-names>Anthony F.</given-names></name>
<name><surname>Davies</surname>
<given-names>G. L. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>498</fpage>
<lpage>502</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000498">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000498">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydrocarbons. Ionisation constants for some substituted 9-phenylfluorenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000503</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cockerill</surname>
<given-names>Anthony F.</given-names></name>
<name><surname>Lamper</surname>
<given-names>John E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>503</fpage>
<lpage>507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000503">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000503">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the decomposition of pyridiniomethylthallium(III) species in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Vamplew</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>507</fpage>
<lpage>514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 stoicheiometry of steroidal ketone–benzene association complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000515</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feeney</surname>
<given-names>J.</given-names></name>
<name><surname>Pauwels</surname>
<given-names>P. J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>515</fpage>
<lpage>518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXI. Acyloxylation, plumbylation, and oxidative dimerisation of some benzenoid compounds in the presence of trifluoro- or trichloro-acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000518</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>
<name><surname>Willson</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>518</fpage>
<lpage>529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000518">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000518">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 LVII. Negative-ion mass spectrometry of functional groups. Simple esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000530</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ho</surname>
<given-names>A. C.</given-names></name>
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Fry</surname>
<given-names>Arthur</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>530</fpage>
<lpage>533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000530">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000530">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effect of 4-substitution on the thermodynamics of hydration of phenol and the phenoxide anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000533</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parsons</surname>
<given-names>G. H.</given-names></name>
<name><surname>Rochester</surname>
<given-names>C. H.</given-names></name>
<name><surname>Wood</surname>
<given-names>C. E. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>533</fpage>
<lpage>536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000533">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000533">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part V. Partial rate factors for protodesilylation of biphenylene: a novel polycyclic reactivity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>536</fpage>
<lpage>538</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal unimolecular isomerization of tricyclo[4,1,0,0&lt;sup&gt;1,3&lt;/sup&gt;]heptane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000539</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Frey</surname>
<given-names>H. M.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>R. G.</given-names></name>
<name><surname>Skattebøl</surname>
<given-names>Lars</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>539</fpage>
<lpage>541</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000539">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000539">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 uncatalysed &lt;i&gt;syn&lt;/i&gt;–&lt;i&gt;anti&lt;/i&gt;-isomerization of imine systems. Part IV. A theoretical study of the influence of substituents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000541</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kerek</surname>
<given-names>F.</given-names></name>
<name><surname>Ostrogovich</surname>
<given-names>G.</given-names></name>
<name><surname>Simon</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>541</fpage>
<lpage>544</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000541">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000541">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 sulphones. Part XI. Extensive delocalisation in benzo- and dibenzo-thiopyran &lt;i&gt;SS&lt;/i&gt;-dioxide anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000545</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradamante</surname>
<given-names>(Mrs.) S.</given-names></name>
<name><surname>Mangia</surname>
<given-names>A.</given-names></name>
<name><surname>Pagani</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>545</fpage>
<lpage>548</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of the &lt;i&gt;C&lt;/i&gt; form of stearic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000548</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Malta</surname>
<given-names>Viscardo</given-names></name>
<name><surname>Celotti</surname>
<given-names>Giancarlo</given-names></name>
<name><surname>Zannetti</surname>
<given-names>Roberto</given-names></name>
<name><surname>Martelli</surname>
<given-names>Adele Ferrero</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>548</fpage>
<lpage>553</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000548">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000548">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isoxazoles from nitrile oxides and arylacetylenes. Kinetics of the reaction of &lt;i&gt;p&lt;/i&gt;-chlorobenzonitrile &lt;i&gt;N&lt;/i&gt;-oxide with phenyl- and mesityl-acetylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battaglia</surname>
<given-names>A.</given-names></name>
<name><surname>Dondoni</surname>
<given-names>A.</given-names></name>
<name><surname>Mangini</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>554</fpage>
<lpage>557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 benzimidazoles. Part VII. Kinetics and mechanism of the reaction of thiophenoxydehalogenation of &lt;i&gt;NN&lt;/i&gt;′-disubstituted 2-chlorobenzimidazolium perchlorates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000557</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dembech</surname>
<given-names>P.</given-names></name>
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
<name><surname>Seconi</surname>
<given-names>G.</given-names></name>
<name><surname>Vivarelli</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>557</fpage>
<lpage>560</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000557">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000557">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of 2-phenylisatogen &lt;i&gt;N&lt;/i&gt;-oxime: crystal and molecular structure of the 4-bromobenzoylation product of 2-phenylisatogen &lt;i&gt;N&lt;/i&gt;-oxime</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000560</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sax</surname>
<given-names>M.</given-names></name>
<name><surname>Pletcher</surname>
<given-names>J.</given-names></name>
<name><surname>Scholtz</surname>
<given-names>D.</given-names></name>
<name><surname>Gerkin</surname>
<given-names>R. M.</given-names></name>
<name><surname>Pinkus</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>560</fpage>
<lpage>564</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000560">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000560">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 between the carbonyl group and an α-sulphur atom. Part I. Infrared and ultraviolet spectra of some α-(alkylthio)thioesters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wladislaw</surname>
<given-names>B.</given-names></name>
<name><surname>Viertler</surname>
<given-names>H.</given-names></name>
<name><surname>Demant</surname>
<given-names>E. Berthold</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>565</fpage>
<lpage>566</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 studies of some asymmetrically substituted 1,3-dioxans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000567</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>V. I. P.</given-names></name>
<name><surname>Ladd</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>567</fpage>
<lpage>570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000567">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000567">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dipole moments and infrared spectra of a series of 4′-substituted 4-hydroxyazobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000570</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Colinese</surname>
<given-names>D. C.</given-names></name>
<name><surname>Ibbitson</surname>
<given-names>D. A.</given-names></name>
<name><surname>Stone</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>570</fpage>
<lpage>574</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000570">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000570">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Association of some aromatic aldehydes and ketones with benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000574</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hopkins</surname>
<given-names>P. 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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>574</fpage>
<lpage>576</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000574">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000574">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 pyrolysis of 1,2-dichloroethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holbrook</surname>
<given-names>K. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. W.</given-names></name>
<name><surname>Watson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>577</fpage>
<lpage>582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylarylnitrosamines. Part I. Electron spin resonance studies relevant to the mechanism of decomposition of acylarylnitrosamines in various solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000583</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Paton</surname>
<given-names>R. M.</given-names></name>
<name><surname>Thomson</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>583</fpage>
<lpage>595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000583">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000583">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylarylnitrosamines. Part II. The formation of arynes in the anomalous decompositions of &lt;i&gt;o&lt;/i&gt;-t-butyl- and 2,5-di-t-butyl-&lt;i&gt;N&lt;/i&gt;-nitrosoacetanilide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000595</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Cook</surname>
<given-names>J.</given-names></name>
<name><surname>Harger</surname>
<given-names>M. J. P.</given-names></name>
<name><surname>Hibbert</surname>
<given-names>P. G.</given-names></name>
<name><surname>Sharp</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>595</fpage>
<lpage>601</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylarylnitrosamines. Part III. Decomposition of 2,5-di-(&lt;i&gt;N&lt;/i&gt;-nitrosoacetamido)-1,4-di-t-butylbenzene and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000602</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Harger</surname>
<given-names>M. J. P.</given-names></name>
<name><surname>Sharp</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>602</fpage>
<lpage>607</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000602">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000602">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the thermal decomposition of difluoroacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000607</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>
<name><surname>Tomlinson</surname>
<given-names>A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>607</fpage>
<lpage>610</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000607">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000607">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reactions of silicon compounds. Part VII. Unimolecular gas-phase thermal decomposition of 2,2-difluoroethyltrimethoxysilane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000611</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Graham</surname>
<given-names>D.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>611</fpage>
<lpage>612</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000611">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000611">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 gas phase reactions of methylspiro[2,2]pentane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000612</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>M. C.</given-names></name>
<name><surname>Gibbons</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>612</fpage>
<lpage>617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000612">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000612">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid-catalysed decarboxylation of phosphonoformic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000618</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Warren</surname>
<given-names>Stuart</given-names></name>
<name><surname>Williams</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>618</fpage>
<lpage>621</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000618">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000618">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Measurement of electrophilic aromatic reactivities &lt;i&gt;via&lt;/i&gt; pyrolysis of 1-arylethyl acetates. Part V. Abnormal deactivation by some &lt;i&gt;ortho&lt;/i&gt;-substituents: the direct field effect</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000622</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>622</fpage>
<lpage>627</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000622">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000622">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vibrational spectra and structure of the rhodizonate dianion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000627</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>R. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>627</fpage>
<lpage>629</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000627">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000627">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 chemical shifts of protons γ to a halogen atom in steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lack</surname>
<given-names>Ruth E.</given-names></name>
<name><surname>Nemorin</surname>
<given-names>J.</given-names></name>
<name><surname>Ridley</surname>
<given-names>Anne B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>629</fpage>
<lpage>631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;X&lt;/i&gt;-ray studies of terpenoids. Part III. A redetermination of the crystal structure of (+)-3-bromocamphor: the absolute configuration of (+)-camphor</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000632</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>F. H.</given-names></name>
<name><surname>Rogers</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>632</fpage>
<lpage>636</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000632">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000632">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactivities of hydrogen peroxide and the hydroperoxide ion towards 3,4-benzotropolone-1′,2′-quinone anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000637</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collier</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>637</fpage>
<lpage>640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000637">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000637">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 8,12-diethyl-2,3,7,13,17,18-hexamethylcorrole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000640</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harrison</surname>
<given-names>H. R.</given-names></name>
<name><surname>Hodder</surname>
<given-names>O. J. R.</given-names></name>
<name><surname>Hodgkin</surname>
<given-names>Dorothy Crowfoot</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>640</fpage>
<lpage>645</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reaction of ethoxycarbonylcarbene with n-hexadecane and n-docosane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000646</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>A. D.</given-names></name>
<name><surname>Wood</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>646</fpage>
<lpage>652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000646">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000646">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Properties of some disulphones: acidities, rates of ionization and bromination, and hydrogen isotope effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Cox</surname>
<given-names>B. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>652</fpage>
<lpage>656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aminoacyl insertion reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000657</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Russell</surname>
<given-names>Peter L.</given-names></name>
<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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>657</fpage>
<lpage>661</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000657">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000657">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 electrophilic substitution at a saturated carbon atom. Part XV. The displacement of an iron carbonyl group from saturated carbon by mercury(II) and thallium(III) species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000662</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dodd</surname>
<given-names>D.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>662</fpage>
<lpage>667</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000662">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000662">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rearrangements of pinane derivatives. Part I. Products of acid catalysed hydration of α-pinene and β-pinene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000668</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>Claudia M.</given-names></name>
<name><surname>Whittaker</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>668</fpage>
<lpage>672</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000668">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000668">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rearrangements of pinane derivatives. Part II. Products of acid-catalysed rearrangement of α-pinene and β-pinene in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000672</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>Claudia M.</given-names></name>
<name><surname>Whittaker</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>672</fpage>
<lpage>677</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000672">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000672">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidation of hydroxamic acids by alkaline ferricyanide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000677</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oliver</surname>
<given-names>T. R.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>677</fpage>
<lpage>681</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000677">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000677">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>π-Electron ‘ring currents’ and proton chemical shifts in planar, condensed, benzenoid hydrocarbons: an empirical reassessment of the semi-classical theory</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000681</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mallion</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>681</fpage>
<lpage>686</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000681">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000681">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deamination of &lt;i&gt;endo&lt;/i&gt;- and &lt;i&gt;exo&lt;/i&gt;-bornylamines and related reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000687</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Morris</surname>
<given-names>D. G.</given-names></name>
<name><surname>Bunton</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>687</fpage>
<lpage>691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000687">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000687">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>π-SCF studies of the circular dichroism and electronic spectra of alkaloids containing the aniline chromophore. The stereochemical configuration of calycanthine and caracurine-II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000691</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brickell</surname>
<given-names>W. S.</given-names></name>
<name><surname>Mason</surname>
<given-names>S. F.</given-names></name>
<name><surname>Roberts</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>691</fpage>
<lpage>695</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000691">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000691">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unusual shielding effects in some 2-phenylsulphonamido-&lt;i&gt;NN&lt;/i&gt;-dialkylanilinium ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000696</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>I.</given-names></name>
<name><surname>Cameron</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>696</fpage>
<lpage>698</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000696">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000696">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 organometallic reactions. Part II. The kinetics and rate constants for the autoxidation of organoboron compounds in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000698</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Ingold</surname>
<given-names>K. U.</given-names></name>
<name><surname>Roberts</surname>
<given-names>B. P.</given-names></name>
<name><surname>Tudor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>698</fpage>
<lpage>712</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000698">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000698">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inductive and field effects in aromatic substitution. Part I. Kinetics of nitration of 4-phenylpyridine and 4-benzylpyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sarlo</surname>
<given-names>F. De</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>712</fpage>
<lpage>715</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inductive and field effects in aromatic substitution. Part II. Nitration of benzotrichloride and βββ-trichloroethylbenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000716</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grynkiewicz</surname>
<given-names>G.</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>716</fpage>
<lpage>719</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000716">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000716">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inductive and field effects in aromatic substitution. Part III. Comparison of the substituents X and CH&lt;sub&gt;2&lt;/sub&gt;X in nitration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000719</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sarlo</surname>
<given-names>F. De</given-names></name>
<name><surname>Grynkiewicz</surname>
<given-names>G.</given-names></name>
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>719</fpage>
<lpage>723</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000719">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000719">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rotational isomerism. Part X. Steric effects on rotamer populations in &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-1,3-dichloroprop-1-enes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000724</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
<name><surname>Parry</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>724</fpage>
<lpage>729</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000724">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000724">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Long-range interactions. Part III. A comparison of arene and olefin as neighbouring groups towards an allylic anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000730</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. M.</given-names></name>
<name><surname>Cain</surname>
<given-names>E. N.</given-names></name>
<name><surname>McIvor</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>730</fpage>
<lpage>733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000730">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000730">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nuclear magnetic resonance study of aromatic substituent effects in 1-X-2,4-dimethylbenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000733</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Socrates</surname>
<given-names>G.</given-names></name>
<name><surname>Adlard</surname>
<given-names>M. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>733</fpage>
<lpage>735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000733">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 J-band of 1,1′-diethyl-9-methyl-4,5;4′,5′-dibenzthiacarbocyanine chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>R. E.</given-names></name>
<name><surname>Gardner</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>736</fpage>
<lpage>738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydrolysis of 2-naphthyl β-D-glucuronide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>B.</given-names></name>
<name><surname>Ghosh</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>739</fpage>
<lpage>740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000739">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the hydrolysis of esters of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-2-hydroxycyclopentanecarboxylic acid and 3-hydroxybutyric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000741</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>Brian</given-names></name>
<name><surname>Page</surname>
<given-names>Michael I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>741</fpage>
<lpage>744</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000741">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000741">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nitration of diphenyl sulphoxide in concentrated sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000745</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marziano</surname>
<given-names>N. C.</given-names></name>
<name><surname>Maccarone</surname>
<given-names>E.</given-names></name>
<name><surname>Passerini</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>745</fpage>
<lpage>747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000745">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000745">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Factors in the formation of isomerically and optically pure alkyl halides. Part VII. Rearrangements occurring during the thermal decomposition of alkyl chloroformates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clinch</surname>
<given-names>P. W.</given-names></name>
<name><surname>Hudson</surname>
<given-names>H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>747</fpage>
<lpage>751</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Configuration of the &lt;i&gt;S&lt;/i&gt;-alkyl thiohydroximates: crystal and molecular structures of &lt;i&gt;syn&lt;/i&gt;-(alkylthio)-isomers of &lt;i&gt;S&lt;/i&gt;-methyl and &lt;i&gt;S&lt;/i&gt;-cyanoethyl &lt;i&gt;O&lt;/i&gt;-(&lt;i&gt;N&lt;/i&gt;-methylcarbamoyl)acetothiohydroximates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000752</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waite</surname>
<given-names>M. G.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>752</fpage>
<lpage>756</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000752">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000752">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enhancement of double-bond participation in the solvolysis of 9-isopropylidene-&lt;i&gt;endo&lt;/i&gt;-3,4-benzotricyclo[4,2,1,0&lt;sup&gt;2,5&lt;/sup&gt;]non-3-en-7-yl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonates by the effect of nonbonded interactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000757</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>R.</given-names></name>
<name><surname>Salter</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>757</fpage>
<lpage>761</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000757">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000757">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Microscopic reversibility and the symmetrical isotopic exchange reactions of organometallic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>M. H.</given-names></name>
<name><surname>Dodd</surname>
<given-names>D.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Lewis</surname>
<given-names>E. S.</given-names></name>
<name><surname>O'Ferrall</surname>
<given-names>R. A. More</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>762</fpage>
<lpage>766</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nucleophilic exchange reactions. Part I. Heterogeneous catalysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000767</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bovington</surname>
<given-names>C. H.</given-names></name>
<name><surname>Maundrell</surname>
<given-names>D. F.</given-names></name>
<name><surname>Dacre</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>767</fpage>
<lpage>770</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000767">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000767">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nitroso-compounds. Part II. The nitrosation of phenol and anisole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000770</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Challis</surname>
<given-names>B. C.</given-names></name>
<name><surname>Lawson</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>770</fpage>
<lpage>775</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000770">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000770">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Methyl proton resonance in nuclear magnetic resonance spectra of 2,2′- and 8,8′-dimethyl-1,1′-binaphthyls. The optical stability of (+)-2,2′-dimethyl-1,1′-binaphthyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000775</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dixon</surname>
<given-names>W.</given-names></name>
<name><surname>Harris</surname>
<given-names>Margaret M.</given-names></name>
<name><surname>Mazengo</surname>
<given-names>R. Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>775</fpage>
<lpage>778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000775">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000775">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrolysis of oxaziridines. Part I. The kinetics of 2-t-butyloxaziridines in strong acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000778</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>Anthony R.</given-names></name>
<name><surname>Challis</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>778</fpage>
<lpage>782</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000778">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000778">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Primary hydrogen isotope effects on the rate of ionization of nitroethane in mixtures of water and dimethyl sulphoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000783</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Cox</surname>
<given-names>B. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>783</fpage>
<lpage>785</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000783">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000783">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;O&lt;/i&gt;-acylglycosyl halides. Part VIII. Exchange reactions of &lt;i&gt;O&lt;/i&gt;-acetylglycosyl bromides with lithium bromide in acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000785</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duffy</surname>
<given-names>M. J.</given-names></name>
<name><surname>Pass</surname>
<given-names>G.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>785</fpage>
<lpage>788</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000785">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000785">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitramines and nitramides. Part XVI. A note on the irreversible decomposition of nitrourea in acidic solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000788</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewhurst</surname>
<given-names>F.</given-names></name>
<name><surname>Lamberton</surname>
<given-names>Alex H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>788</fpage>
<lpage>789</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000788">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000788">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 effect of alkyl substitution on ionisation potential</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000790</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocksey</surname>
<given-names>B. J.</given-names></name>
<name><surname>Eland</surname>
<given-names>J. H. D.</given-names></name>
<name><surname>Danby</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>790</fpage>
<lpage>792</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000790">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000790">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 spectra of some julolidine (2,3,6,7-tetrahydro-1&lt;i&gt;H&lt;/i&gt;, 5&lt;i&gt;H&lt;/i&gt;-benzo[&lt;i&gt;ij&lt;/i&gt;]quinolizine) analogues of 4-dimethylaminoazobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000793</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Castelino</surname>
<given-names>R. W.</given-names></name>
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>793</fpage>
<lpage>795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000793">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000793">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazepines. Part XIII. Relative reactivities of positions 5 and 6 in electrophilic substitution reactions of 2,3-dihydro-1,4-diazepinium salts measured by deuterium exchange kinetics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000795</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>Anthony R.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
<name><surname>Marshall</surname>
<given-names>Donald R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>795</fpage>
<lpage>797</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000795">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000795">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 β-keto-enol ethers with bromine in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000797</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marshall</surname>
<given-names>D. R.</given-names></name>
<name><surname>Roberts</surname>
<given-names>T. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>797</fpage>
<lpage>800</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000797">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000797">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chromogens based on non-benzenoid aromatic systems. Part I. Electronic absorption spectra of 5-phenylazotropolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000801</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>801</fpage>
<lpage>805</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000801">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000801">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dipole moments and molecular conformation in aromatic diazoketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000805</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sorriso</surname>
<given-names>S.</given-names></name>
<name><surname>Piazza</surname>
<given-names>G.</given-names></name>
<name><surname>Foffani</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>805</fpage>
<lpage>809</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000805">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000805">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 radiolysis of ethanol–ethylene systems. Part I. Telomerisation reactions at low pressures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000809</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Basson</surname>
<given-names>R. A.</given-names></name>
<name><surname>Wyk</surname>
<given-names>L. van</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>809</fpage>
<lpage>813</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000809">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000809">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Relative rates of the concurrent reactions in the addition of a substituted benzonitrile oxide to arylacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beltrame</surname>
<given-names>P.</given-names></name>
<name><surname>Sartirana</surname>
<given-names>P.</given-names></name>
<name><surname>Vintani</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>814</fpage>
<lpage>817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Symmetrically bifurcate hydrogen bonding. Part I. Bis-(β-acylvinyl)-amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dąbrowski</surname>
<given-names>Janusz</given-names></name>
<name><surname>Świstun</surname>
<given-names>Zofia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>818</fpage>
<lpage>821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 VII. Replacement of the trimethylammonio group in substituted purines by hydroxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000821</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Young</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>821</fpage>
<lpage>826</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000821">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000821">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydrolysis and aminolysis of &lt;i&gt;N&lt;/i&gt;-acetyl-&lt;i&gt;O&lt;/i&gt;-formylserinamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000826</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackburn</surname>
<given-names>G. M.</given-names></name>
<name><surname>Dodds</surname>
<given-names>H. L. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>826</fpage>
<lpage>831</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000826">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000826">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 1-methyl-4-phosphorinanone and 1-methyl-4-piperidone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000832</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Quin</surname>
<given-names>Louis D.</given-names></name>
<name><surname>Toube</surname>
<given-names>Trevor P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>832</fpage>
<lpage>834</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000832">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000832">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 separation of polar and steric effects. Part XII. The influence of protic and aprotic solvents on the kinetics of the reactions of benzoic acid with diazodiphenylmethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000834</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Dack</surname>
<given-names>M. R. J.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>834</fpage>
<lpage>842</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000834">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000834">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 4,7-di-(2-thienyl)-4,5,6,7-tetrahydrobenzo[&lt;i&gt;b&lt;/i&gt;]thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000843</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hawley</surname>
<given-names>David M.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>George</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>843</fpage>
<lpage>846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000843">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000843">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 preparation and spectroscopic properties of 2,2,4,5-tetramethylhex-4-en-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000846</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Al-Jallo</surname>
<given-names>H. N. A.</given-names></name>
<name><surname>Arnold</surname>
<given-names>B. J.</given-names></name>
<name><surname>Rothwell</surname>
<given-names>B. J.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>846</fpage>
<lpage>847</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000846">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000846">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 attack on 4-aminomethyleneoxazol-5(4&lt;i&gt;H&lt;/i&gt;)-ones, a rationalisation of penicillin carcinogenicity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000848</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Longridge</surname>
<given-names>J. L.</given-names></name>
<name><surname>Timms</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>848</fpage>
<lpage>851</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000848">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000848">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Penicillenic acid, the mechanism of the acid and base catalysed hydrolysis reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000852</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Longridge</surname>
<given-names>J. L.</given-names></name>
<name><surname>Timms</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>852</fpage>
<lpage>857</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000852">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000852">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrogen bonding and substituent group effects in phénols. Part I. Apparent dipole moments and infrared spectra of &lt;i&gt;N&lt;/i&gt;-(4-hydroxybenzylidene)-4-substituted-anilines in benzene, carbon tetrachloride, and dioxan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000857</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Colinese</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>857</fpage>
<lpage>863</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000857">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000857">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrogen bonding and substituent group effects in phenols. Part II. Apparent dipole moments and infrared spectra of &lt;i&gt;N&lt;/i&gt;-(4-substituted benzylidene)-4-hydroxyanilines in benzene, carbon tetrachloride, and dioxan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000864</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Colinese</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>864</fpage>
<lpage>869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000864">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000864">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 LX. The conformation of 5&lt;i&gt;H&lt;/i&gt;-dibenzo[&lt;i&gt;a,d&lt;/i&gt;]cyclohepten-5-one and 10,11-dihydro-5&lt;i&gt;H&lt;/i&gt;-dibenzo[&lt;i&gt;a,d&lt;/i&gt;]cyclohepten-5-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000869</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Weiler-Feilchenfeld</surname>
<given-names>Hannah</given-names></name>
<name><surname>Solomonovici</surname>
<given-names>Abraham</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>869</fpage>
<lpage>871</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000869">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000869">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 attacks on carbon–carbon double bonds. Part XIII. Vinylic substitution of 1,1-dicyano-2-&lt;i&gt;p&lt;/i&gt;-dimethylaminophenyl-2-halogenoethylenes by aromatic amines in acetonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000871</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
<name><surname>Ta-Shma</surname>
<given-names>Rachel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>871</fpage>
<lpage>881</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000871">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000871">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 yttrium(III) catalysed hydrolysis of acid phosphonate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000881</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blewett</surname>
<given-names>F. McC.</given-names></name>
<name><surname>Watts</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>881</fpage>
<lpage>885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000881">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000881">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mass spectrometry. Part XIV. The effect of conformation on the electron impact-induced fragmentation of adducts of &lt;i&gt;p&lt;/i&gt;-benzoquinone and 1,1′-bicycloalkenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000886</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deutsch</surname>
<given-names>Joseph</given-names></name>
<name><surname>Mandelbaum</surname>
<given-names>Asher</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>886</fpage>
<lpage>889</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000886">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000886">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 adsorption as the first step in the solid-state oxidation of benzenehexol with active manganese dioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fatiadi</surname>
<given-names>Alexander J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>889</fpage>
<lpage>894</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 8-carboxy-1-hydroxy-2-oxobicyclo-[3,2,2]non-6-ene-9,4-carbolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pointer</surname>
<given-names>D. J.</given-names></name>
<name><surname>Wilford</surname>
<given-names>J. B.</given-names></name>
<name><surname>Chui</surname>
<given-names>K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>895</fpage>
<lpage>898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 effect of solvent on the electronic absorption spectra of the mesoionic compounds 2,3-diphenyl-2&lt;i&gt;H&lt;/i&gt;-tetrazolium-5-thiolate and 4-phenyl-1,3,4-thiadiazolium-2-thiolate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000898</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiwan</surname>
<given-names>A. M.</given-names></name>
<name><surname>Irving</surname>
<given-names>H. M. N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>898</fpage>
<lpage>901</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000898">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000898">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 decomposition of bis-1,5-diphenylformazan-3-yl disulphide and bis-4-phenyl-Δ&lt;sup&gt;2&lt;/sup&gt;-1,3,4-thiadiazolin-2-yl disulphide in organic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000901</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiwan</surname>
<given-names>A. M.</given-names></name>
<name><surname>Irving</surname>
<given-names>H. M. N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>901</fpage>
<lpage>903</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000901">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000901">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Annulenes. Part XII. The dianion of [12]annulene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000904</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oth</surname>
<given-names>J. F. M.</given-names></name>
<name><surname>Schröder</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>904</fpage>
<lpage>907</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000904">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000904">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 motions in solid 1,6-anhydro-β-D-glucopyranose by &lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000908</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>George W.</given-names></name>
<name><surname>Shafizadeh</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>908</fpage>
<lpage>911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000908">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000908">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;N&lt;/i&gt;-(6-chlorophthalan-1-ylidene)-1-(methylazo)cyclohexylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000911</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Remoortere</surname>
<given-names>F. P. van</given-names></name>
<name><surname>Boer</surname>
<given-names>F. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>911</fpage>
<lpage>918</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000911">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000911">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure in the crystalline state of a dicarbonium ion containing two triphenylmethylium ion groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000918</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McKechnie</surname>
<given-names>James S.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>918</fpage>
<lpage>924</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000918">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000918">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2,6-Dinitro-4-X-anilino-&lt;i&gt;N&lt;/i&gt;-methylpropionamides: reactions with amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>J. J. K.</given-names></name>
<name><surname>McFarlane</surname>
<given-names>N. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>925</fpage>
<lpage>928</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2,6-Dinitro-4-X-anilino-&lt;i&gt;N&lt;/i&gt;-methylpropionamides: reactions with potassium methoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000928</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>J. J. K.</given-names></name>
<name><surname>Jewess</surname>
<given-names>P. J.</given-names></name>
<name><surname>McFarlane</surname>
<given-names>N. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>928</fpage>
<lpage>930</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000928">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000928">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 photochemistry of 4-phenylbut-1-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000931</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Salisbury</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>931</fpage>
<lpage>935</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000931">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000931">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of buxenine-G. &lt;i&gt;X&lt;/i&gt;-ray diffraction studies of buxenine-G dihydrobromide and dihydroiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000935</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>Waite</surname>
<given-names>M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>935</fpage>
<lpage>941</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000935">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000935">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of &lt;i&gt;p&lt;/i&gt;-bromophenylimino(triphenyl)phosphorane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000942</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewlins</surname>
<given-names>M. J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>942</fpage>
<lpage>945</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000942">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000942">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structures of 3,5-epidithio-2-nitroso-1,5-diphenylpenta-2,4-dien-1-one and 2,4-epidithio-1-nitro-1-nitroso-4-phenylbutadiene: heterocycles with a very short S ⋯ O intramolecular distance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000946</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>Paul L.</given-names></name>
<name><surname>Reid</surname>
<given-names>Kenneth I. G.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>946</fpage>
<lpage>952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000946">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000946">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 1-bromo-2,4-epidithio-1-nitro-4-phenylbutadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000952</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Reid</surname>
<given-names>Kenneth I. G.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>952</fpage>
<lpage>957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000952">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000952">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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-catalysed formation of monoacetals from n-butyraldehyde and certain D-glucitol derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000957</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>Bourne</surname>
<given-names>E. J.</given-names></name>
<name><surname>Cleare</surname>
<given-names>P. J. V.</given-names></name>
<name><surname>Cole</surname>
<given-names>R. F. J.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>957</fpage>
<lpage>962</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000957">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000957">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic and acetylenic compounds. Part VI. The electron impact-induced rearrangements of substituted phenylacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000962</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Safe</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>962</fpage>
<lpage>965</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000962">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000962">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Classical carbonium ions. Part II. Synthesis, properties, and solvolysis of alkyl picrates and related compounds. A comparison of arenesulphonate and phenoxide leaving groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000965</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sinnott</surname>
<given-names>M. L.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>965</fpage>
<lpage>975</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000965">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000965">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 4-acetylamino-2-bromo-5-isopropyl-1-methylimidazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000976</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Remoortere</surname>
<given-names>F. P. van</given-names></name>
<name><surname>Boer</surname>
<given-names>F. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>976</fpage>
<lpage>980</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000976">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000976">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 orbital calculations of aromatic reactivity. Part I. π-Electron calculations for monosubstituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000981</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howe</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>981</fpage>
<lpage>984</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000981">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000981">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 orbital calculations of aromatic reactivity. Part II. All-valence-electron calculations for monosubstituted benzenes: an analysis of the sigma inductive effect</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000984</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howe</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>984</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000984">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000984">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chromic acid oxidation of polycyclic alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000988</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>R.</given-names></name>
<name><surname>Mason</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>988</fpage>
<lpage>993</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000988">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000988">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXIX. Alkylamino and α-amino-alkyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710000993</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>N. H.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>993</fpage>
<lpage>1003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710000993">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710000993">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXX. One-electron reduction of carbonyl-containing compounds by the radicals ·CO&lt;sub&gt;2&lt;/sub&gt;H, ·CO&lt;sub&gt;2&lt;/sub&gt;&lt;sup&gt;–&lt;/sup&gt;, and ·CMe&lt;sub&gt;2&lt;/sub&gt;·NH&lt;sub&gt;2&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>N. H.</given-names></name>
<name><surname>Dobbs</surname>
<given-names>A. J.</given-names></name>
<name><surname>Edge</surname>
<given-names>D. J.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>West</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1004</fpage>
<lpage>1008</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXI. The generation, and some reactions, of the radicals SO&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;–·&lt;/sup&gt;, S&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;–·&lt;/sup&gt;, S&lt;sup&gt;–·&lt;/sup&gt;, and SH in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001009</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Storey</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1009</fpage>
<lpage>1013</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001009">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001009">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 trifluoroacetamide and &lt;i&gt;N&lt;/i&gt;-methyltrifluoroacetamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001014</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akiyama</surname>
<given-names>H.</given-names></name>
<name><surname>Yamauchi</surname>
<given-names>F.</given-names></name>
<name><surname>Ouchi</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1014</fpage>
<lpage>1018</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001014">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001014">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ion pairing in alkali-metal salts of 1,3-diphenylbut-1-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burley</surname>
<given-names>J. W.</given-names></name>
<name><surname>Young</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1018</fpage>
<lpage>1024</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Isolation of 4,5,4′,5′-tetrachlorobi-1,3-dioxa-2-cyclopentyl from reaction of &lt;i&gt;trans&lt;/i&gt;-2,3-dichloro-1,4-dioxan with sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001024</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huang</surname>
<given-names>H. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1024</fpage>
<lpage>1028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001024">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001024">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ring inversion in bishexahydropyrimidylmethanes. An interesting case of diastereotopism due to slow ring inversion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001028</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1028</fpage>
<lpage>1030</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbon-13 nuclear magnetic resonance spectra of some 1,3-dioxans. Part II. A demonstration of non-chair conformations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kellie</surname>
<given-names>G. M.</given-names></name>
<name><surname>Riddell</surname>
<given-names>F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1030</fpage>
<lpage>1034</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbonates. Part XI. Conformational and other effects of substitution in the acid-catalysed hydrolysis of highly branched ethylene and trimethylene carbonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001035</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katzhendler</surname>
<given-names>J.</given-names></name>
<name><surname>Poles</surname>
<given-names>(the late) L. A.</given-names></name>
<name><surname>Dagan</surname>
<given-names>H.</given-names></name>
<name><surname>Sarel</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1035</fpage>
<lpage>1040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001035">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001035">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Strain energy effects in the gas-phase elimination reactions of cycloalkyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dakubu</surname>
<given-names>M.</given-names></name>
<name><surname>Holmes</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1040</fpage>
<lpage>1042</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 on the relative stabilities of 1:1 and 1:2 adducts formed from 1,3,5-trinitrobenzene and thiolate ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001043</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>M. R.</given-names></name>
<name><surname>Ghariani</surname>
<given-names>M. El.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1043</fpage>
<lpage>1047</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001043">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001043">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 preparation of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-1-alkyl-4-phthalimidocyclohexanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>H.</given-names></name>
<name><surname>Gidley</surname>
<given-names>G. C.</given-names></name>
<name><surname>Thornburrow</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1047</fpage>
<lpage>1050</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 cyclic compounds. Part VII. The effect of axial alkyl groups in causing a flattening of the cyclohexane ring in &lt;i&gt;cis&lt;/i&gt;-1-alkyl-4-phthalimidocyclohexanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001051</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>H.</given-names></name>
<name><surname>Thornburrow</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1051</fpage>
<lpage>1058</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001051">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001051">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 some aryl cobalt nitroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001059</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swanwick</surname>
<given-names>M. G.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1059</fpage>
<lpage>1064</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001059">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001059">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 infrared study on benzeneseleninic acids and salts: assignments and substituent effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001065</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Filippo</surname>
<given-names>D. De</given-names></name>
<name><surname>Momicchioli</surname>
<given-names>F.</given-names></name>
<name><surname>Rastelli</surname>
<given-names>A.</given-names></name>
<name><surname>Preti</surname>
<given-names>C.</given-names></name>
<name><surname>Verani</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1065</fpage>
<lpage>1069</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001065">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001065">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amaryllidaceae alkaloids. Part II. Crystal structure of tazettine methiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001070</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sato</surname>
<given-names>T.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1070</fpage>
<lpage>1073</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001070">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001070">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 thalidomide, &lt;i&gt;N&lt;/i&gt;-(α-glutarimido)-phthalimide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001073</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>F. H.</given-names></name>
<name><surname>Trotter</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1073</fpage>
<lpage>1079</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001073">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001073">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 a bis-&lt;i&gt;p&lt;/i&gt;-bromobenzoate derivative of cyclograndisolide [3α-methoxy-9,19-cyclo-9β-lanost-24-en-27,23(&lt;i&gt;R&lt;/i&gt;)-olide]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001079</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>F. H.</given-names></name>
<name><surname>Trotter</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1079</fpage>
<lpage>1084</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001079">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001079">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Configuration of the endocyclic double-bond and conformation of the germacranolide dilactones, isabelin, isoisabelin, and related germacranolide monolactones, as studied by nuclear Overhauser effect</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tori</surname>
<given-names>Kazuo</given-names></name>
<name><surname>Horibe</surname>
<given-names>Isao</given-names></name>
<name><surname>Yoshioka</surname>
<given-names>Hirosuke</given-names></name>
<name><surname>Mabry</surname>
<given-names>Tom J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1084</fpage>
<lpage>1088</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of Friedel–Crafts acylating agents. Part I. Two novel methods of measuring reaction rates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001088</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pettiford</surname>
<given-names>L. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1088</fpage>
<lpage>1091</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular catalysis of phosphate triester hydrolysis. Nucleophilic catalysis by the neighbouring carboxyl group of the hydrolysis of dialkyl 2-carboxyphenyl phosphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001091</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bromilow</surname>
<given-names>R. H.</given-names></name>
<name><surname>Khan</surname>
<given-names>S. A.</given-names></name>
<name><surname>Kirby</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1091</fpage>
<lpage>1097</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acetaldehyde azine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001098</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gowenlock</surname>
<given-names>B. G.</given-names></name>
<name><surname>Haynes</surname>
<given-names>R. M.</given-names></name>
<name><surname>Johnson</surname>
<given-names>C. A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1098</fpage>
<lpage>1102</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001098">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001098">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Configuration of the &lt;i&gt;S&lt;/i&gt;-alkyl thiohydroximates: crystal-structure analysis of the &lt;i&gt;syn&lt;/i&gt;-(alkylthio)-isomer of &lt;i&gt;S&lt;/i&gt;-cyanoethyl acetothiohydroximate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001102</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waite</surname>
<given-names>M. G.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1102</fpage>
<lpage>1105</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001102">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001102">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the hydrolysis of 3,1-benzoxazin-4-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001105</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>A.</given-names></name>
<name><surname>Salvadori</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1105</fpage>
<lpage>1110</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001105">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001105">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 III. Reactions of trimethyl-, dimethylphenyl-, methyldiphenyl-, and triphenyl-silyl-lithium with fluorene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001110</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Hamid</surname>
<given-names>M. A.</given-names></name>
<name><surname>Rees</surname>
<given-names>N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1110</fpage>
<lpage>1114</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001110">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001110">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reduction of aldehydes and ketones. Part XIII. Effect of hydration and carbanion–enolate formation on the electrolysis of glycolaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001114</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnes</surname>
<given-names>D.</given-names></name>
<name><surname>Uden</surname>
<given-names>P. C.</given-names></name>
<name><surname>Zuman</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1114</fpage>
<lpage>1117</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001114">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001114">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reduction of aldehydes and ketones. Part XIV. Formation of &lt;i&gt;trans&lt;/i&gt;- and &lt;i&gt;cis&lt;/i&gt;-crotyl alcohol in the electroreduction of crotonaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001118</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnes</surname>
<given-names>D.</given-names></name>
<name><surname>Zuman</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1118</fpage>
<lpage>1121</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001118">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001118">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 with rearrangement. Part III. Isotope effects in the prototropic rearrangement of 4-bromo-2,6-di-t-butylcyclohexa-2,5-dienone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Singh</surname>
<given-names>A.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
<name><surname>Zeltner</surname>
<given-names>Michal</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1122</fpage>
<lpage>1129</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvolysis of &lt;i&gt;syn&lt;/i&gt;-&lt;i&gt;endo&lt;/i&gt;-tricyclo[3,2,1,0&lt;sup&gt;2,4&lt;/sup&gt;]oct-6-en-8-yl &lt;i&gt;p&lt;/i&gt;-nitrobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001129</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jovanovich</surname>
<given-names>Andrew P.</given-names></name>
<name><surname>Lambert</surname>
<given-names>Joseph B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1129</fpage>
<lpage>1132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001129">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001129">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 dipole moments, molar Kerr constants, and conformations as solutes of thioanisole and some &lt;i&gt;para&lt;/i&gt;-substituted thioanisoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001132</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Pierens</surname>
<given-names>R. K.</given-names></name>
<name><surname>The</surname>
<given-names>(Miss) Mida G. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1132</fpage>
<lpage>1135</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001132">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001132">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 stereochemistry of 2-alkoxy-4-methyl-1,3,2-dioxaphosphorinans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bodkin</surname>
<given-names>C. L.</given-names></name>
<name><surname>Simpson</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1136</fpage>
<lpage>1141</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydrolysis of some acid phthalic and acid terephthalic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anantaraman</surname>
<given-names>R.</given-names></name>
<name><surname>Nair</surname>
<given-names>T. D. Radhakrishnan</given-names></name>
<name><surname>Saramma</surname>
<given-names>(Miss) K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1142</fpage>
<lpage>1143</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbon–carbon bond participation in the solvolysis of &lt;i&gt;exo&lt;/i&gt;-2,3-&lt;i&gt;o&lt;/i&gt;-arylene-5-norbornyl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001144</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>R.</given-names></name>
<name><surname>Mason</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1144</fpage>
<lpage>1150</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001144">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001144">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effect of solvent and temperature upon the emission spectra of aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001151</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davidson</surname>
<given-names>R. S.</given-names></name>
<name><surname>Santhanam</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1151</fpage>
<lpage>1154</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001151">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001151">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XLVI. Interpretation of the substituent effects in base-catalysed cleavage of aryltrimethyl-silanes and -stannanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001155</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bassindale</surname>
<given-names>A. R.</given-names></name>
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
<name><surname>Thompson</surname>
<given-names>A. R.</given-names></name>
<name><surname>Walton</surname>
<given-names>D. R. M.</given-names></name>
<name><surname>Cretney</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1155</fpage>
<lpage>1161</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001155">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001155">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 isomerisation of dimethyl sulphite to methyl methanesulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001161</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brook</surname>
<given-names>A. J. W.</given-names></name>
<name><surname>Robertson</surname>
<given-names>R. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1161</fpage>
<lpage>1163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001161">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001161">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 on the acid-catalysed inversion of sucrose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnett</surname>
<given-names>J. W.</given-names></name>
<name><surname>O'Connor</surname>
<given-names>Charmain J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1163</fpage>
<lpage>1165</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidation of ethyl mandelate by chromic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001166</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jha</surname>
<given-names>D. S.</given-names></name>
<name><surname>Bakore</surname>
<given-names>G. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1166</fpage>
<lpage>1168</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001166">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001166">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 phosphate esters of biological importance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001168</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tidd</surname>
<given-names>B. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1168</fpage>
<lpage>1176</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001168">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001168">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 gas-phase thermal decomposition of chlorodifluoromethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001176</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnes</surname>
<given-names>G. R.</given-names></name>
<name><surname>Cox</surname>
<given-names>R. A.</given-names></name>
<name><surname>Simmons</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1176</fpage>
<lpage>1180</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001176">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001176">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 1,1-di-(&lt;i&gt;p&lt;/i&gt;-nitrophenyl)ethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001180</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casalone</surname>
<given-names>G.</given-names></name>
<name><surname>Simonetta</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1180</fpage>
<lpage>1183</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001180">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001180">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Trapping and identification of the intermediate aryl radicals from the reaction of aroylarylhydrazines (arylarenecarbohydrazides) with sodium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001183</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Neville</surname>
<given-names>A. F.</given-names></name>
<name><surname>Russell</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1183</fpage>
<lpage>1187</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001183">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001183">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 methyl radicals with triethylborane in the gas phase</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001187</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grotewold</surname>
<given-names>J.</given-names></name>
<name><surname>Lissi</surname>
<given-names>E. A.</given-names></name>
<name><surname>Scaiano</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1187</fpage>
<lpage>1191</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001187">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001187">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the reaction of cyclopentadienylidenetriarylphosphoranes with cyano-olefins. Part IV. Tricyanovinylation of cyclopentadienylidenetriphenylphosphorane with tetracyanoethylene and tricyanovinyl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001192</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rigby</surname>
<given-names>C. W.</given-names></name>
<name><surname>Lord</surname>
<given-names>E.</given-names></name>
<name><surname>Naan</surname>
<given-names>M. P.</given-names></name>
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1192</fpage>
<lpage>1197</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001192">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001192">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Conformations of the chlorobenzaldehydes and chloroacetophenones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001198</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheng</surname>
<given-names>C. L.</given-names></name>
<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>Goodman</surname>
<given-names>P. A.</given-names></name>
<name><surname>Gore</surname>
<given-names>P. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1198</fpage>
<lpage>1201</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001198">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001198">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 saturated systems. Basicity, reactivity, and stereochemistry in 3- and 6-substituted &lt;i&gt;cis&lt;/i&gt;-hexahydrocarbazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001201</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>A.</given-names></name>
<name><surname>Utley</surname>
<given-names>J. H. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1201</fpage>
<lpage>1207</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001201">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001201">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Orbital steering: an unnecessary concept</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001207</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>Brian</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1207</fpage>
<lpage>1209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001207">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001207">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of t-butyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001209</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>J. E.</given-names></name>
<name><surname>Pearson</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1209</fpage>
<lpage>1211</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001209">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001209">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acetoxylation of arenes. Part VI. Formation of 4-nitrocyclohexa-2,5-dienones in the nitration of bromo-, acetoxy- and methoxy-arenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001212</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackstock</surname>
<given-names>D. J.</given-names></name>
<name><surname>Hartshorn</surname>
<given-names>M. P.</given-names></name>
<name><surname>Lewis</surname>
<given-names>A. J.</given-names></name>
<name><surname>Richards</surname>
<given-names>K. E.</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1212</fpage>
<lpage>1213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001212">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001212">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reactions in cyclic systems. Displacement reactions of some sterically hindered tosylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001214</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rothberg</surname>
<given-names>Irvin</given-names></name>
<name><surname>Russo</surname>
<given-names>Robert V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1214</fpage>
<lpage>1218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001214">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001214">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of narcissidine methiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001218</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Immirzi</surname>
<given-names>A.</given-names></name>
<name><surname>Fuganti</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1218</fpage>
<lpage>1220</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001218">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001218">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 parameters and aromatic systems. Part III. Reactivity relationships, and their application to substituent effects in aromatic systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001221</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bancroft</surname>
<given-names>K. C. C.</given-names></name>
<name><surname>Howe</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1221</fpage>
<lpage>1227</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001221">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001221">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 conformation of the amide group in &lt;i&gt;N&lt;/i&gt;-acyl-indolines and -1,2,3,4-tetrahydroquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Monro</surname>
<given-names>A. M.</given-names></name>
<name><surname>Sewell</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1227</fpage>
<lpage>1230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 3,4-dihydro-2&lt;i&gt;H&lt;/i&gt;-1,5-benzodioxepin, and its derivatives as determined from their ultraviolet absorption spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001231</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Archer</surname>
<given-names>A. W.</given-names></name>
<name><surname>Claret</surname>
<given-names>P. A.</given-names></name>
<name><surname>Hayman</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1231</fpage>
<lpage>1240</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001231">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001231">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rotational isomerism. Part XI. The nuclear magnetic resonance spectra and rotational isomerism of 1,2-difluoro- and 1,1,2-trifluoroethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001240</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
<name><surname>Kemp</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1240</fpage>
<lpage>1245</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001240">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001240">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Magnetic non-equivalence in the nuclear magnetic resonance spectra of 2-cyanoethyl(phenyl)-1-phenylethylphosphine and &lt;i&gt;NO&lt;/i&gt;-dimethyl-&lt;i&gt;N&lt;/i&gt;-(1-phenylethyl)hydroxylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001246</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Powell</surname>
<given-names>R. L.</given-names></name>
<name><surname>Posner</surname>
<given-names>T.</given-names></name>
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1246</fpage>
<lpage>1249</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001246">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001246">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rearrangements of pinane derivatives. Part III. Solvolysis of the 2-pinanyl &lt;i&gt;p&lt;/i&gt;-nitrobenzoates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001249</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Salmon</surname>
<given-names>J. R.</given-names></name>
<name><surname>Whittaker</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1249</fpage>
<lpage>1254</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heteroaromatic reactivity. Part V. A quantitative study of the products of nitration of the quinolinium ion in sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001254</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crout</surname>
<given-names>D. H. G.</given-names></name>
<name><surname>Penton</surname>
<given-names>J. R.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1254</fpage>
<lpage>1256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001254">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001254">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part VII. A critical re-examination of the reactivity of toluene towards nitration with acetyl nitrate in acetic anhydride, as determined by the kinetic and competition methods</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001256</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>S. R.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1256</fpage>
<lpage>1261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001256">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001256">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;N&lt;/i&gt;-heterocycles. Pyridazinones and pyridazinethiones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Young</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1261</fpage>
<lpage>1264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 pyrolysis and the solvolysis of s-butyl thiocyanate. Part I. The gas-phase pyrolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barroeta</surname>
<given-names>N.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Cavazza</surname>
<given-names>M.</given-names></name>
<name><surname>Congiu</surname>
<given-names>L.</given-names></name>
<name><surname>Fava</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1264</fpage>
<lpage>1267</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 thio- and isothio-cyanates. Part III. Pyrolysis of s-butyl isothiocyanate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001267</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barroeta</surname>
<given-names>N.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>A.</given-names></name>
<name><surname>Cavazza</surname>
<given-names>M.</given-names></name>
<name><surname>Congiu</surname>
<given-names>L.</given-names></name>
<name><surname>Fava</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1267</fpage>
<lpage>1269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001267">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001267">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001270</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Isaacs</surname>
<given-names>N. W.</given-names></name>
<name><surname>Kennard</surname>
<given-names>C. H. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1270</fpage>
<lpage>1273</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001270">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001270">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nitrophenyl(phenyl)methanes: the formation of an &lt;i&gt;M&lt;/i&gt;–17 ion from the &lt;i&gt;meta&lt;/i&gt;- and &lt;i&gt;para&lt;/i&gt;-isomers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001273</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robinson</surname>
<given-names>G. E.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. B.</given-names></name>
<name><surname>Vernon</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1273</fpage>
<lpage>1282</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001273">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001273">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Magnetic non-equivalence in nuclear resonance. Part V. Geminal allenic protons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>Maryvonne L.</given-names></name>
<name><surname>Martin</surname>
<given-names>Gérard J.</given-names></name>
<name><surname>Couffignal</surname>
<given-names>René</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1282</fpage>
<lpage>1283</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 constants of organic charge-transfer complexes derived from optical and from nuclear magnetic resonance chemical shift measurements; the presence of termolecular complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001283</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dodson</surname>
<given-names>B.</given-names></name>
<name><surname>Foster</surname>
<given-names>R.</given-names></name>
<name><surname>Bright</surname>
<given-names>A. A. S.</given-names></name>
<name><surname>Foreman</surname>
<given-names>M. I.</given-names></name>
<name><surname>Gorton</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1283</fpage>
<lpage>1293</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001283">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001283">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Enol elimination reactions. Part V. A study of the mechanism of the decarboxylative elimination reactions of some enol sulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001293</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>Ian</given-names></name>
<name><surname>Owen</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1293</fpage>
<lpage>1299</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001293">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001293">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXX. 3-Alkyl tetrahydro-1,3-oxazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001300</article-id><contrib-group><contrib contrib-type="author">
<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>Trepanier</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1300</fpage>
<lpage>1302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001300">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001300">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXI. 1-t-Butylpiperidine-4-spiro-4′-(1′,3′-dioxolan) and 1,3-dioxan-5-spiro-4′-(1′,3′-dioxolan)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001302</article-id><contrib-group><contrib contrib-type="author">
<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>Lehman</surname>
<given-names>P. G.</given-names></name>
<name><surname>Record</surname>
<given-names>K. A. F.</given-names></name>
<name><surname>Shapiro</surname>
<given-names>(Mrs) B. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1302</fpage>
<lpage>1307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXII. 1-t-Butylpiperidine-4-spiro-4′- and -5′-oxazolines and -4′- and -5′- thiazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001308</article-id><contrib-group><contrib contrib-type="author">
<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>Lehman</surname>
<given-names>P. G.</given-names></name>
<name><surname>Shapiro</surname>
<given-names>(Mrs.) B. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1308</fpage>
<lpage>1315</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXIII. 1-t-Butylpiperidine-4-spiro-4′- and -5′-(2′,2′-dimethyloxazolidine) and a discussion of steric compression effects on chemical shifts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001316</article-id><contrib-group><contrib contrib-type="author">
<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>Lehman</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1316</fpage>
<lpage>1320</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001316">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001316">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXIV. The influence of lone pair orientation on the differential proton chemical shift of adjacent methylene groups and on &lt;i&gt;J&lt;/i&gt;&lt;sub&gt;gem&lt;/sub&gt; values</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001320</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Halls</surname>
<given-names>P. J.</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>Snarey</surname>
<given-names>M.</given-names></name>
<name><surname>Trepanier</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1320</fpage>
<lpage>1324</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001320">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001320">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXV. 1-Phenoxymethyl-3,4-dihydroisoquinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001325</article-id><contrib-group><contrib contrib-type="author">
<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>Shapiro</surname>
<given-names>B. B.</given-names></name>
<name><surname>Tute</surname>
<given-names>M. S.</given-names></name>
<name><surname>Gadsby</surname>
<given-names>B.</given-names></name>
<name><surname>Broadbent</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1325</fpage>
<lpage>1327</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001325">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001325">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXVI. The rotamer populations of axial cyclohexylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>M. J.</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>Markees</surname>
<given-names>D. G.</given-names></name>
<name><surname>Richards</surname>
<given-names>A. C.</given-names></name>
<name><surname>Jacks</surname>
<given-names>L. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1327</fpage>
<lpage>1330</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXVIII. &lt;i&gt;N&lt;/i&gt;-alkylpiperidine and &lt;i&gt;N&lt;/i&gt;-alkylmorpholine &lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001330</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>M. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Manas</surname>
<given-names>M. Moreno</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1330</fpage>
<lpage>1334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001330">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001330">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 pyridine-catalysed methanolysis of aromatic sulphonyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogne</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1334</fpage>
<lpage>1337</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polarography of organic cations in acid solution. Part II. Various aralkyl ions in sulphuric and methanesulphonic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001337</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Plesch</surname>
<given-names>P. H.</given-names></name>
<name><surname>Šestáková</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1337</fpage>
<lpage>1342</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of taxinine: &lt;i&gt;X&lt;/i&gt;-ray analysis of 2,5,9,10-tetra-&lt;i&gt;O&lt;/i&gt;-acetyl-14-bromotaxinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001342</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shiro</surname>
<given-names>M.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1342</fpage>
<lpage>1346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001342">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001342">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;2′ mechanism. Chloride ion-catalysed isomerization of α- and &lt;i&gt;γ&lt;/i&gt;-methylallyl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hemmingson</surname>
<given-names>J. A.</given-names></name>
<name><surname>England</surname>
<given-names>(the late) B. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1347</fpage>
<lpage>1352</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001347">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 glycolaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001352</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>G. C. S.</given-names></name>
<name><surname>George</surname>
<given-names>W. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1352</fpage>
<lpage>1355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001352">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001352">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of keto–enol equilibria. Part XIII. &lt;sup&gt;15&lt;/sup&gt;N-substituted imines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001356</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dudek</surname>
<given-names>Gerald</given-names></name>
<name><surname>Dudek</surname>
<given-names>Emily Pitcher</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1356</fpage>
<lpage>1360</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001356">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001356">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>σρ Relationships in the ultraviolet spectra of 4-R-, 5-R-, and 6-R-2-nitrodiphenyl sulphides in methanol and in cyclohexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001360</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Porto</surname>
<given-names>A. M.</given-names></name>
<name><surname>Altieri</surname>
<given-names>L.</given-names></name>
<name><surname>Castro</surname>
<given-names>A. J.</given-names></name>
<name><surname>Brieux</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1360</fpage>
<lpage>1366</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001360">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001360">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polysaccharide conformation. Part VII. Model building computations for α-1,4 galacturonan and the kinking function of L-rhamnose residues in pectic substances</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001366</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rees</surname>
<given-names>D. A.</given-names></name>
<name><surname>Wight</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1366</fpage>
<lpage>1372</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001366">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001366">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of 2-halogenothiazoles towards nucleophiles: kinetics and mechanisms of the reactions of 2-halogeno-X-thiazoles with benzenethiolate ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bosco</surname>
<given-names>M.</given-names></name>
<name><surname>Forlani</surname>
<given-names>L.</given-names></name>
<name><surname>Liturri</surname>
<given-names>V.</given-names></name>
<name><surname>Riccio</surname>
<given-names>P.</given-names></name>
<name><surname>Todesco</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1373</fpage>
<lpage>1376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Micellar effects on the rates of formation and decomposition of the hydroxy Meisenheimer complex of 1,3,6,8-tetranitronaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001377</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Casilio</surname>
<given-names>L. M.</given-names></name>
<name><surname>Fendler</surname>
<given-names>E. J.</given-names></name>
<name><surname>Fendler</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1377</fpage>
<lpage>1380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001377">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001377">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;-substituted heterocyclic cations. Part IX. The preparation and chloride-ion catalysed unimolecular acidolysis of 2-[chloromercury(II)]-1,3-dimethylbenzimidazolium ions in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooksey</surname>
<given-names>C. J.</given-names></name>
<name><surname>Dodd</surname>
<given-names>D.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1380</fpage>
<lpage>1384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 anhydrosulphites of α-hydroxycarboxylic acids. Part VII. Polymerisation of anhydrosulphites derived from symmetrically substituted α-hydroxy-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blackbourn</surname>
<given-names>G. P.</given-names></name>
<name><surname>Tighe</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1384</fpage>
<lpage>1390</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ring–chain tautomerism. Part I. 2-Acyl- and 2-aroyl-benzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001390</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1390</fpage>
<lpage>1394</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001390">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001390">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ring–chain tautomerism. Part II. Methyl esters of 2-acyl-and 2-aroyl-benzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001395</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1395</fpage>
<lpage>1399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001395">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001395">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XII. Stereochemistry of gaillardin: crystal and molecular structures of bromogaillardin and deacetyldihydrogaillardin &lt;i&gt;p&lt;/i&gt;-bromobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001399</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dullforce</surname>
<given-names>T. A.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
<name><surname>White</surname>
<given-names>D. N. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1399</fpage>
<lpage>1405</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001399">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001399">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pyrrole studies. Part XVI. Conformational studies of 6-aryl-6-di-methylamino-2-azafulvenes [2-aryl(dimethylamino)methylenepyrroles]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Candy</surname>
<given-names>C. F.</given-names></name>
<name><surname>Jones</surname>
<given-names>R. Alan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1405</fpage>
<lpage>1406</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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, molecular, and electronic structure of 2,5-diphenyl-1,4-dithiin 1-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001407</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bandoli</surname>
<given-names>G.</given-names></name>
<name><surname>Panattoni</surname>
<given-names>C.</given-names></name>
<name><surname>Clemente</surname>
<given-names>D. A.</given-names></name>
<name><surname>Tondello</surname>
<given-names>E.</given-names></name>
<name><surname>Dondoni</surname>
<given-names>A.</given-names></name>
<name><surname>Mangini</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1407</fpage>
<lpage>1411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001407">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001407">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 geometric isomerisation about azomethine bonds. Part II. Bromination of &lt;i&gt;NN&lt;/i&gt;-disubstituted hydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Groeger</surname>
<given-names>F. A.</given-names></name>
<name><surname>Hegarty</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1411</fpage>
<lpage>1417</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 p&lt;i&gt;K&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; values of mono-substituted phenols and benzenethiols and the conjugation of substituents having a strong +&lt;i&gt;K&lt;/i&gt; effect</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001417</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chuchani</surname>
<given-names>G.</given-names></name>
<name><surname>Frohlich</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1417</fpage>
<lpage>1420</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001417">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001417">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 phosphorescent centres in biphenyl, biphenyl–tetracyanoethylene, and biphenyl–tetracyanoethylene–naphthalene molecular crystals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haines</surname>
<given-names>R. M.</given-names></name>
<name><surname>Pryce</surname>
<given-names>A.</given-names></name>
<name><surname>Shields</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1420</fpage>
<lpage>1424</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ionization constants of heterocyclic substances. Part IX. Protonation of aminopyridones and aminopyrimidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001425</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Pfleiderer</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1425</fpage>
<lpage>1432</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001425">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001425">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 data and deviations from coplanarity of helicene molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001433</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laarhoven</surname>
<given-names>W. H.</given-names></name>
<name><surname>Brus</surname>
<given-names>G. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1433</fpage>
<lpage>1434</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001433">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001433">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acyl sulphonate reactions. Part III. The solvolyses of acyl sulphonates and sulphonic anhydrides, both cyclic and acyclic, in hydroxylic solvents, and the reaction of acetyl benzenesulphonate with a series of 3- and 4-substituted anilines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001434</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Laird</surname>
<given-names>R. M.</given-names></name>
<name><surname>Spence</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1434</fpage>
<lpage>1440</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001434">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001434">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structures of complexes between alkali-metal salts and cyclic polyethers. Part II. Complex formed from sodium bromide and 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacyclo-octadeca-2,11-diene (‘di-benzo-18-crown-6’)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001440</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bush</surname>
<given-names>M. A.</given-names></name>
<name><surname>Truter</surname>
<given-names>Mary R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1440</fpage>
<lpage>1446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001440">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001440">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part VI. Protodesilylation and protodetritiation of some oxygen- and sulphur-containing aromatic compounds and of diphenylmethane. Evidence for hyperconjugation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>F. P.</given-names></name>
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1446</fpage>
<lpage>1449</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Measurement of electrophilic aromatic reactivities &lt;i&gt;via&lt;/i&gt; pyrolysis of 1-arylethyl acetates. Part VI. Further evidence for the direct field effect, and the invalidity of σ&lt;sub&gt;&lt;i&gt;0&lt;/i&gt;&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt; values</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001450</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1450</fpage>
<lpage>1454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001450">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001450">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Structural implications of nuclear magnetic resonance and infrared investigations on 2-substituted 1,3,2-dioxaphosphorinan-2-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>White</surname>
<given-names>D. W.</given-names></name>
<name><surname>McEwen</surname>
<given-names>G. K.</given-names></name>
<name><surname>Bertrand</surname>
<given-names>R. D.</given-names></name>
<name><surname>Verkade</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1454</fpage>
<lpage>1461</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 attacks on carbon–carbon double bonds. Part XIV. Low-element effects and amine catalysis in the substitution of 1,1-dicyano-2-&lt;i&gt;p&lt;/i&gt;-dimethylaminophenyl-2-halogenoethylenes by anilines in alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001461</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
<name><surname>Ta-Shma</surname>
<given-names>Rachel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1461</fpage>
<lpage>1467</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001461">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001461">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 spectra of some analogues and derivatives of Michler's ketone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001468</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Castelino</surname>
<given-names>R. W.</given-names></name>
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1468</fpage>
<lpage>1471</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001468">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001468">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deviations in the electronic absorption spectra of di- and tri-arylmethane dyes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001471</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Castelino</surname>
<given-names>R. W.</given-names></name>
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1471</fpage>
<lpage>1473</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001471">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001471">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Purines, pyrimidines, and imidazoles. Part XXXVIII. A kinetics study of the decarboxylation of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxylic acid 5′-phosphate and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001474</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Litchfield</surname>
<given-names>G. J.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1474</fpage>
<lpage>1484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001474">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001474">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 X. Electron spin resonance study of the radical anions of azobenzene, naphthalene-1-azobenzene, 1,1′-azonaphthalene, and 2,2′-azonaphthalene including the measurements of tight ion-pair–loose ion-pair equilibria</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001484</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>Emes</surname>
<given-names>P. J.</given-names></name>
<name><surname>James</surname>
<given-names>C. L.</given-names></name>
<name><surname>Pomery</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1484</fpage>
<lpage>1493</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001484">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001484">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heteroaromatic reactivity. Part VI. Kinetics and products of the nitration of 4-hydroxyquinoline, 1-methyl-4-quinolone, 4-methoxyquinoline, and 4-hydroxycinnoline in sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001493</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Penton</surname>
<given-names>J. R.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1493</fpage>
<lpage>1498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001493">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001493">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 dipole moments, molar Kerr constants, and conformations as solutes of substituted phenylcyclopropanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armstrong</surname>
<given-names>R. S.</given-names></name>
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Hector</surname>
<given-names>(Miss) A.</given-names></name>
<name><surname>Hopkins</surname>
<given-names>P.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Lüttke</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1499</fpage>
<lpage>1502</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effect of unsaturated substituents on the hydrolysis of esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001502</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>C. G.</given-names></name>
<name><surname>Thomas</surname>
<given-names>J. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1502</fpage>
<lpage>1504</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001502">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001502">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Decomposition reactions of sodium propionate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001505</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duruz</surname>
<given-names>J. J.</given-names></name>
<name><surname>Michels</surname>
<given-names>H. J.</given-names></name>
<name><surname>Ubbelohde</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1505</fpage>
<lpage>1509</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001505">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001505">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 triplet state of LSD and its 2-bromo-derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowd</surname>
<given-names>A.</given-names></name>
<name><surname>Hudson</surname>
<given-names>J. B.</given-names></name>
<name><surname>Turnbull</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1509</fpage>
<lpage>1510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ion-pair dissociation equilibria for hexachloroantimonate salts of stable organic cations in dichloromethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001511</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowyer</surname>
<given-names>P. M.</given-names></name>
<name><surname>Ledwith</surname>
<given-names>A.</given-names></name>
<name><surname>Sherrington</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1511</fpage>
<lpage>1514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001511">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001511">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;ortho&lt;/i&gt;-Effects on ordering factors in mass spectral rearrangements. Loss of keten from halogenated phenyl acetates and acetanilides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001515</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Benezra</surname>
<given-names>Steven A.</given-names></name>
<name><surname>Bursey</surname>
<given-names>Maurice M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1515</fpage>
<lpage>1520</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 II. Theoretical calculation and experimental measurement of halogen exchange of 1-halogeno-2,4-dinitrobenzenes in methanol and &lt;i&gt;NN&lt;/i&gt;-dimethylformamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001521</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>
<name><surname>Wong</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1521</fpage>
<lpage>1525</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001521">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001521">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of &lt;i&gt;N&lt;/i&gt;-(&lt;i&gt;p&lt;/i&gt;-bromophenylcarbamoyl)thiamine anhydride (&lt;i&gt;N&lt;/i&gt;,&lt;i&gt;S&lt;/i&gt;-&lt;i&gt;trans&lt;/i&gt;-type)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001525</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nakai</surname>
<given-names>H.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1525</fpage>
<lpage>1529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001525">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001525">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazepines. Part XIV. Reactivities of positions 5 and 6 in 2,3-dihydro-1,4-diazepines towards quasi-aromatic substitution by bromine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnett</surname>
<given-names>C.</given-names></name>
<name><surname>Marshall</surname>
<given-names>D. R.</given-names></name>
<name><surname>Mulligan</surname>
<given-names>L. A.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1529</fpage>
<lpage>1533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Field and charge-transfer theory for the quantitative correlation of substituent effects in aromatic molecules. Part I. The field and charge-transfer (FCT) theory</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001534</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1534</fpage>
<lpage>1537</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001534">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001534">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Field and charge-transfer theory for the quantitative correlation of substituent effects in aromatic molecules. Part II. Photoelectron spectra of substituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001537</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1537</fpage>
<lpage>1540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001537">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001537">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Field and charge-transfer theory for the quantitative correlation of substituent effects in aromatic molecules. Part III. Thermal heterolytic addition and elimination reactions of substituted benzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001540</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1540</fpage>
<lpage>1544</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Field and charge-transfer theory for the quantitative correlation of substituent effects in aromatic molecules. Part IV. Non-additivity in electrophilic substitution reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001545</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1545</fpage>
<lpage>1547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphines. Part III. Kinetics of oxidation of thiobenzophenones with peroxybenzoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001547</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battaglia</surname>
<given-names>A.</given-names></name>
<name><surname>Dondoni</surname>
<given-names>A.</given-names></name>
<name><surname>Giorgianni</surname>
<given-names>P.</given-names></name>
<name><surname>Maccagnani</surname>
<given-names>G.</given-names></name>
<name><surname>Mazzanti</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1547</fpage>
<lpage>1550</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001547">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001547">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Barriers to ring inversion in two alkoxy-1,3-dioxans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001551</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eccleston</surname>
<given-names>G.</given-names></name>
<name><surname>Wyn-Jones</surname>
<given-names>E.</given-names></name>
<name><surname>Orville-Thomas</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1551</fpage>
<lpage>1552</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001551">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001551">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXXI. Formation of cyclo-octa-1,5-&lt;i&gt;cis&lt;/i&gt;,&lt;i&gt;cis&lt;/i&gt;-dienes from 1,4-disubstituted &lt;i&gt;s&lt;/i&gt;-&lt;i&gt;trans&lt;/i&gt;-butadienes in the solid state. A contribution to the problem of C&lt;sub&gt;4&lt;/sub&gt;-&lt;i&gt;versus&lt;/i&gt; C&lt;sub&gt;8&lt;/sub&gt;-cyclodimerisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001552</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Green</surname>
<given-names>B. S.</given-names></name>
<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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1552</fpage>
<lpage>1564</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001552">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001552">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of new alkaloids, secodaphniphylline and methyl homosecodaphniphyllate: &lt;i&gt;X&lt;/i&gt;-ray analysis of methyl &lt;i&gt;N&lt;/i&gt;-bromoacetylhomosecodaphniphyllate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sasaki</surname>
<given-names>Kyoyu</given-names></name>
<name><surname>Hirata</surname>
<given-names>Yoshimasa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1565</fpage>
<lpage>1568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of vinyl sulphonic esters. Part VI. &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;1-type reactivity of 1,2-diphenyl-2-phenylthiovinyl and triphenylvinyl derivatives: anchimeric assistance due to the β-sulphur atom</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001569</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Tonellato</surname>
<given-names>U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1569</fpage>
<lpage>1573</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001569">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001569">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free-radical reductions of arenediazonium ions in aqueous solution. Part I. Toluene-&lt;i&gt;p&lt;/i&gt;-diazonium ions reduced with methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001574</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Packer</surname>
<given-names>J. E.</given-names></name>
<name><surname>House</surname>
<given-names>D. B.</given-names></name>
<name><surname>Rasburn</surname>
<given-names>E. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1574</fpage>
<lpage>1578</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001574">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001574">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Conformations of 1- and 2-benzoylnaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001579</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cheng</surname>
<given-names>C. L.</given-names></name>
<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>Gore</surname>
<given-names>P. H.</given-names></name>
<name><surname>Yusuf</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1579</fpage>
<lpage>1581</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;p&lt;/i&gt;-chloroanilide derivative of bicyclo[5,3,1]undec-7-en-11-one-1-carboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001581</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>A. Forbes</given-names></name>
<name><surname>Jamieson</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1581</fpage>
<lpage>1585</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001581">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001581">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 comparison of sensitivities to substituent effects of five-membered heteroaromatic rings in gas phase ionization</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001585</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Linda</surname>
<given-names>Paolo</given-names></name>
<name><surname>Marino</surname>
<given-names>Gianlorenzo</given-names></name>
<name><surname>Pignataro</surname>
<given-names>Salvatore</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1585</fpage>
<lpage>1587</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001585">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001585">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nitroaromatic compounds. Part II. An electron spin resonance study of the radical anions of some nitronaphthalic anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001588</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wells</surname>
<given-names>C. H. J.</given-names></name>
<name><surname>Wilson</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1588</fpage>
<lpage>1592</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001588">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001588">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anodic oxidation of amines. Part II. Electrochemical dealkylation of aliphatic tertiary amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Masui</surname>
<given-names>Masaichiro</given-names></name>
<name><surname>Sayo</surname>
<given-names>Hiroteru</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1593</fpage>
<lpage>1596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal decomposition of fluoroacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001596</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1596</fpage>
<lpage>1597</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001596">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001596">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of jatrophone dihydrobromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001598</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haltiwanger</surname>
<given-names>R. C.</given-names></name>
<name><surname>Bryan</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1598</fpage>
<lpage>1602</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001598">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001598">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 spectral charateristics of the cyclobutane ring system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zirvi</surname>
<given-names>Karimullah A.</given-names></name>
<name><surname>Jarboe</surname>
<given-names>Charles H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1603</fpage>
<lpage>1606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the formation of hydrazides from hydrazidic halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001607</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Cashman</surname>
<given-names>M.</given-names></name>
<name><surname>Hegarty</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1607</fpage>
<lpage>1610</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001607">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001607">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Standard enthalpies of formation of diphenyl oxalate and benzoic anhydride and some related bond dissociation energies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001611</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carson</surname>
<given-names>A. S.</given-names></name>
<name><surname>Fine</surname>
<given-names>D. H.</given-names></name>
<name><surname>Gray</surname>
<given-names>P.</given-names></name>
<name><surname>Laye</surname>
<given-names>P. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1611</fpage>
<lpage>1615</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001611">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001611">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazepines. Part XV. Polarographic studies on six 2,3-dihydro-1,4-diazepinium perchlorates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001615</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cleghorn</surname>
<given-names>H. P.</given-names></name>
<name><surname>Gaskin</surname>
<given-names>J. E.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>Douglas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1615</fpage>
<lpage>1617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001615">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001615">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereospecific electronegative effects. Part I. The &lt;sup&gt;19&lt;/sup&gt;F nuclear magnetic resonance spectra of deoxyfluoro-D-glucopyranoses</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001618</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Phillips</surname>
<given-names>L.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1618</fpage>
<lpage>1624</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001618">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001618">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 protonation of some oxygenated derivatives of hemimellitene (1,2,3-trimethylbenzene) and &lt;i&gt;o&lt;/i&gt;-xylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001624</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>M. P.</given-names></name>
<name><surname>Richards</surname>
<given-names>K. E.</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1624</fpage>
<lpage>1625</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001624">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001624">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 gas-phase thermal decomposition of bromodifluoromethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001625</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>R. A.</given-names></name>
<name><surname>Simmons</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1625</fpage>
<lpage>1631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001625">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001625">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 analysis of indan-1-ols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hiscock</surname>
<given-names>M.</given-names></name>
<name><surname>Porter</surname>
<given-names>G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1631</fpage>
<lpage>1634</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cathodic reduction of the trityl cation in methylene dichloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001634</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Plesch</surname>
<given-names>P. H.</given-names></name>
<name><surname>Stasko</surname>
<given-names>A.</given-names></name>
<name><surname>Robson</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1634</fpage>
<lpage>1637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001634">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001634">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitroxide radicals. Part IX. Preparation of [2,2]paracyclophane mono- and bis-nitroxides and [2,2]paracyclophanequinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forrester</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ramasseul</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1638</fpage>
<lpage>1644</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitroxide radicals. Part X. Electron spin resonance spectra of [2,2]paracyclophanylene bisnitroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001645</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forrester</surname>
<given-names>A. R.</given-names></name>
<name><surname>Ramasseul</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1645</fpage>
<lpage>1647</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001645">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001645">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;-imines, &lt;i&gt;C&lt;/i&gt;-ylides, and anhydrobases derived from 1,2,4-triazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001648</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyd</surname>
<given-names>G. V.</given-names></name>
<name><surname>Summers</surname>
<given-names>A. J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1648</fpage>
<lpage>1654</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Investigation of unimolecular decomposition and isomerisation reactions of some metastable carboxonium ions in the gas phase</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001654</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mead</surname>
<given-names>Timothy J.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1654</fpage>
<lpage>1658</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001654">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001654">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 some radical anion intermediates from xanthen and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001659</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tabner</surname>
<given-names>B. J.</given-names></name>
<name><surname>Zdysiewicz</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1659</fpage>
<lpage>1664</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001659">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001659">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deuterium solvent isotope effects in methanol solution. Part I. Fractionation factors for lyonium and lyate ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001665</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Grist</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1665</fpage>
<lpage>1670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001665">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001665">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 benzimidazoles. Part VIII. &lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance study of substituted 2-chloro-1-methylbenzimidazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001670</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dembech</surname>
<given-names>P.</given-names></name>
<name><surname>Seconi</surname>
<given-names>G.</given-names></name>
<name><surname>Vivarelli</surname>
<given-names>P.</given-names></name>
<name><surname>Schenetti</surname>
<given-names>L.</given-names></name>
<name><surname>Taddei</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1670</fpage>
<lpage>1675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001670">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001670">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 VIII. Preparation and reactivity of trimethylammonio derivatives of aza monocycles (pyridine and pyrimidine) towards hydroxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001675</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Young</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1675</fpage>
<lpage>1682</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001675">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001675">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the reaction of triarylphosphines with 7,7,8,8-tetracyanoquinodimethane and tetracyanoethylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001683</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Naan</surname>
<given-names>M. P.</given-names></name>
<name><surname>Powell</surname>
<given-names>R. L.</given-names></name>
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1683</fpage>
<lpage>1691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001683">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001683">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbohydrate derivatives. Part III. Crystal and molecular structure of (2&lt;i&gt;R&lt;/i&gt;,4&lt;i&gt;S&lt;/i&gt;,6&lt;i&gt;S&lt;/i&gt;)-2-hydroxymethyl-6-methoxy-1,4-oxathian &lt;i&gt;S&lt;/i&gt;-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001692</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Watkin</surname>
<given-names>D. J.</given-names></name>
<name><surname>Hamor</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1692</fpage>
<lpage>1696</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001692">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001692">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 3,3′-spirobi(bicyclo[3,1,0]hexane)-2,2′-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001696</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Herbstein</surname>
<given-names>F. H.</given-names></name>
<name><surname>Regev</surname>
<given-names>(Mrs) H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1696</fpage>
<lpage>1698</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001696">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001696">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nucleophilic displacement in allylic systems. Part X. Bimolecular substitution with rearrangement: some comments on the &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;2′ mechanism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001699</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Vernon</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1699</fpage>
<lpage>1700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001699">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001699">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of vinyl sulphonic esters. Part VII. Assisted and unassisted &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;1-type reactivity of β-arylthiovinyl sulphonic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001700</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capozzi</surname>
<given-names>G.</given-names></name>
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Tonellato</surname>
<given-names>U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1700</fpage>
<lpage>1704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001700">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001700">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular catalysis in the oxidation of 2-carboxybenzaldehyde with bromine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001704</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>B. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1704</fpage>
<lpage>1707</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001704">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001704">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 acid–base behaviour of cationic indicators in H&lt;sub&gt;2&lt;/sub&gt;O–D&lt;sub&gt;2&lt;/sub&gt;O mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001707</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1707</fpage>
<lpage>1711</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001707">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001707">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidations by chloramine-T. Part I. Oxidation of α-hydroxy-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mushran</surname>
<given-names>S. P.</given-names></name>
<name><surname>Agrawal</surname>
<given-names>M. C.</given-names></name>
<name><surname>Prasad</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1712</fpage>
<lpage>1714</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 studies of alkoxyphosphonium hexachloroantimonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001714</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Murray</surname>
<given-names>M.</given-names></name>
<name><surname>Schmutzler</surname>
<given-names>R.</given-names></name>
<name><surname>Gründemann</surname>
<given-names>E.</given-names></name>
<name><surname>Teichmann</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1714</fpage>
<lpage>1719</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001714">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001714">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free radical substitution in aliphatic compounds. Part XXII. The gasphase chlorination of chlorocyclopentane and methylcyclopentane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001719</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ashton</surname>
<given-names>D. S.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1719</fpage>
<lpage>1722</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001719">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001719">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Free radical substitution in aliphatic compounds. Part XXIII. The gas phase chlorination of chlorocycloheptane and fluorocyclohexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001723</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ashton</surname>
<given-names>D. S.</given-names></name>
<name><surname>Tedder</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1723</fpage>
<lpage>1726</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001723">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001723">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 keten. Part I. Kinetics of the gas-phase reaction with acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001727</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Davies</surname>
<given-names>H. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1727</fpage>
<lpage>1728</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001727">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001727">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reactivities of ‘normal’ and angle strained cyclo-olefins in 1,3-dipolar cycloaddition reactions. Rotational barriers in nitrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001728</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boyle</surname>
<given-names>Lynda W.</given-names></name>
<name><surname>Peagram</surname>
<given-names>M. J.</given-names></name>
<name><surname>Whitham</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1728</fpage>
<lpage>1733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001728">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001728">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 5-methoxycarbonylmethylene-2-piperidino-Δ&lt;sup&gt;2&lt;/sup&gt;-thiazolin-4-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001733</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>A. F.</given-names></name>
<name><surname>Hair</surname>
<given-names>N. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1733</fpage>
<lpage>1736</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001733">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Product ratios in the ring-opening photoreactions of cycloalkanones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coyle</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1736</fpage>
<lpage>1740</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amine oxidation. Part III. The oxidation of some aralkyl tertiary amines with alkaline potassium hexacyanoferrate(III)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001741</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Audeh</surname>
<given-names>C. A.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. R. Lindsay</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1741</fpage>
<lpage>1744</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001741">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001741">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amine oxidation. Part IV. The oxidative cyclisation of trialkylamino-alcohols and -amines with alkaline potassium hexacyanoferrate(III)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001745</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Audeh</surname>
<given-names>C. A.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. R. Lindsay</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1745</fpage>
<lpage>1747</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001745">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001745">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 antioxidant action: the pro-oxidant stage in the function of thiodipropionate esters as antioxidants</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armstrong</surname>
<given-names>Colin</given-names></name>
<name><surname>Scott</surname>
<given-names>Gerald</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1747</fpage>
<lpage>1752</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 phthalides and phthaleins in concentrated sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001752</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hopkinson</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1752</fpage>
<lpage>1756</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001752">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001752">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 serratamolide and related cyclotetradepsipeptides in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001757</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Moschidis</surname>
<given-names>M. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1757</fpage>
<lpage>1761</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001757">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001757">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 pyrolyses of 1,1-dichlorobutane and 1,1-dichloropropane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holbrook</surname>
<given-names>K. A.</given-names></name>
<name><surname>Parry</surname>
<given-names>K. A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1762</fpage>
<lpage>1765</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 in strongly basic solutions. Part II. Correlations of the rates of alkaline hydrolysis of 1-substituted 2- and 4-nitrobenzenes and 4-substituted 1-methoxy-2-nitrobenzenes in aqueous dimethyl sulphoxide with an acidity function</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001765</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Cook</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1765</fpage>
<lpage>1770</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001765">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001765">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 in strongly basic solutions. Part III. Correlation of the rate of alkaline hydrolysis of 1-substituted 2,4-dinitrobenzenes in aqueous dimethyl sulphoxide with an acidity function. Details of the mechanistic pathway</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001771</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Cook</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1771</fpage>
<lpage>1778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001771">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001771">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 in strongly basic solutions. Part IV. Kinetics and mechanisms of the alkaline hydrolysis of 1-substituted 2,4-dinitrobenzenes in aqueous dioxan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001778</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Cook</surname>
<given-names>R. S.</given-names></name>
<name><surname>Price</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1778</fpage>
<lpage>1783</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001778">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001778">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 in strongly basic media. Part V. The kinetics and mechanism of the alkaline hydrolysis of substituted 2-alkoxytropones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001784</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Price</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1784</fpage>
<lpage>1792</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001784">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001784">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 hydrolysis of peroxybenzoic acid in aqueous acidic solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001792</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Secco</surname>
<given-names>F.</given-names></name>
<name><surname>Celsi</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1792</fpage>
<lpage>1795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001792">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001792">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;cis&lt;/i&gt;–&lt;i&gt;trans&lt;/i&gt; Equilibrium in &lt;i&gt;meta&lt;/i&gt;-chlorophenyl aldehydes, ethers, ketones, and carboxylic esters from dipole moment studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001795</article-id><contrib-group><contrib contrib-type="author">
<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>Ochkin</surname>
<given-names>A. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1795</fpage>
<lpage>1799</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001795">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001795">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of mass spectra of organic compounds. Part IX. Evidence against charge localization in the fragmentation of methionine and selenomethionine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001800</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>T. W.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
<name><surname>Mellon</surname>
<given-names>F. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1800</fpage>
<lpage>1803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001800">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001800">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of mass spectra of organic compounds. Part X. Rationalization of a variety of electron-impact induced rearrangements of ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>T. W.</given-names></name>
<name><surname>Johnstone</surname>
<given-names>R. A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1804</fpage>
<lpage>1811</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dielectric relaxation and dipole moments of substituted pyrroles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001811</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Wood</surname>
<given-names>J. W. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1811</fpage>
<lpage>1817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001811">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001811">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 base-catalysed hydrolysis of substituted aryl benzoates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chaw</surname>
<given-names>Z. S.</given-names></name>
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Happer</surname>
<given-names>D. A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1818</fpage>
<lpage>1819</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Negative radicals of condensed thiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001820</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lunazzi</surname>
<given-names>L.</given-names></name>
<name><surname>Placucci</surname>
<given-names>G.</given-names></name>
<name><surname>Tiecco</surname>
<given-names>M.</given-names></name>
<name><surname>Martelli</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1820</fpage>
<lpage>1822</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001820">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001820">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 organometallic reactions. Part III. An electron spin resonance study of homolytic t-butoxydealkylation of organometallic compounds. Rate constants for the reaction at boron</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001823</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Griller</surname>
<given-names>D.</given-names></name>
<name><surname>Roberts</surname>
<given-names>B. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1823</fpage>
<lpage>1829</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001823">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001823">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 organometallic reactions. Part IV. Homolytic alkylthiyldealkylation of organoboranes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001830</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1830</fpage>
<lpage>1837</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001830">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001830">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photo-oxygenation of 4&lt;i&gt;H&lt;/i&gt;-pyran-4-thiones and 4&lt;i&gt;H&lt;/i&gt;-thiopyran-4-thiones: reactivity and kinetic characterization</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001837</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ishibe</surname>
<given-names>N.</given-names></name>
<name><surname>Odani</surname>
<given-names>M.</given-names></name>
<name><surname>Sunami</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1837</fpage>
<lpage>1840</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001837">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001837">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 electrophilic substitution at a saturated carbon atom. Part XVI. Rates of reaction of metallic electrophiles with the 2-, 3-, and 4-pyridiniomethylchromium(III) ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001841</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dodd</surname>
<given-names>D.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Vamplew</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1841</fpage>
<lpage>1846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001841">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001841">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 carbonates. Part XII. The alkaline hydrolysis of highly branched ethylene and trimethylene carbonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001847</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katzhendler</surname>
<given-names>Joshua</given-names></name>
<name><surname>Poles</surname>
<given-names>(the late) L. A.</given-names></name>
<name><surname>Sarel</surname>
<given-names>Shalom</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1847</fpage>
<lpage>1854</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001847">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001847">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the reactions of aromatic sulphonyl chlorides with anilines in methanol; Brønsted and Hammett correlations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogne</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1855</fpage>
<lpage>1858</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 between the carbonyl group and an α-sulphur atom. Part III. Infrared and nuclear magnetic resonance measurements of carbonyl group basicities for some α-ethylthio-substituted carbonyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wladislaw</surname>
<given-names>B.</given-names></name>
<name><surname>Rittner</surname>
<given-names>R.</given-names></name>
<name><surname>Viertler</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1859</fpage>
<lpage>1861</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Succinamic acids. Part I. Hydrogen-bonding equilibria in succinanilic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001862</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>M. J.</given-names></name>
<name><surname>Loadman</surname>
<given-names>M. J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1862</fpage>
<lpage>1865</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001862">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001862">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXI. Butylamine and hydrogen bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001865</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Nagra</surname>
<given-names>S. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1865</fpage>
<lpage>1869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001865">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001865">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XXII. &lt;i&gt;NN&lt;/i&gt;-dimethylformamide and hydrogen chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001869</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Nagra</surname>
<given-names>S. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1869</fpage>
<lpage>1872</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001869">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001869">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 alkylamino-radicals. Part I. Photolysis of dialkylamino-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001873</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>P. W.</given-names></name>
<name><surname>Gesser</surname>
<given-names>H. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1873</fpage>
<lpage>1876</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001873">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001873">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 thermal decomposition of acetic anhydride in flow and static systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001877</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Speis</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1877</fpage>
<lpage>1878</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001877">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001877">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;ortho&lt;/i&gt;-Group participation in azocarbonium ion and 1,3-dipolar ion formation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001879</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hegarty</surname>
<given-names>A. F.</given-names></name>
<name><surname>Cashman</surname>
<given-names>M.</given-names></name>
<name><surname>Aylward</surname>
<given-names>J. B.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1879</fpage>
<lpage>1883</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001879">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001879">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic proton nuclear magnetic resonance spectra. Part VII. [&lt;sup&gt;2&lt;/sup&gt;H&lt;sub&gt;6&lt;/sub&gt;]Benzene-induced solvent shifts at high solute concentration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001884</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Takeuchi</surname>
<given-names>Yoshito</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1884</fpage>
<lpage>1887</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001884">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001884">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Radiation chemistry of aqueous solutions of indole and its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001887</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Iddon</surname>
<given-names>B.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. O.</given-names></name>
<name><surname>Robbins</surname>
<given-names>K. E.</given-names></name>
<name><surname>Davies</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1887</fpage>
<lpage>1892</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001887">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001887">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Addition reactions of conjugated double bonds. Part III. The kinetics of pyrazoline ring formation from αβ-unsaturated phenylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001892</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferres</surname>
<given-names>H.</given-names></name>
<name><surname>Hamdam</surname>
<given-names>M. S.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1892</fpage>
<lpage>1898</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001892">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001892">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nucleophilic character of &lt;i&gt;N&lt;/i&gt;-halogenosulphonamide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001899</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hardy</surname>
<given-names>F. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1899</fpage>
<lpage>1902</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001899">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001899">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;117&lt;/sup&gt;Sn, &lt;sup&gt;119&lt;/sup&gt;Sn Satellite spectra and &lt;sup&gt;117,119&lt;/sup&gt;Sn–H long-range coupling constants in the symmetrical isomers of tetrafuryl- and tetrathienyl-tin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001903</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barbieri</surname>
<given-names>G.</given-names></name>
<name><surname>Taddei</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1903</fpage>
<lpage>1906</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001903">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001903">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 effect of pH on the racemisation rate of 4,4′-biquinolyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001907</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>Malcolm</given-names></name>
<name><surname>Ingle</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1907</fpage>
<lpage>1912</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001907">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001907">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 catalysis. Part IV. Acid-catalysed hydrolysis of some 3-alkylsydnones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001912</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aziz</surname>
<given-names>S.</given-names></name>
<name><surname>Buglass</surname>
<given-names>A. J.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1912</fpage>
<lpage>1916</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001912">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001912">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidation of 1,3-dioxolan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001916</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Molera</surname>
<given-names>M. J.</given-names></name>
<name><surname>Domínguez</surname>
<given-names>J. A. García</given-names></name>
<name><surname>Acuña</surname>
<given-names>A. U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1916</fpage>
<lpage>1923</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001916">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001916">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Dehydration mechanisms in the thermal decomposition of gaseous formic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001923</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Davies</surname>
<given-names>H. H.</given-names></name>
<name><surname>Jackson</surname>
<given-names>G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1923</fpage>
<lpage>1925</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001923">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001923">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 study of some benzeneseleninic acids; kinetics of reduction by iodide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferranti</surname>
<given-names>F.</given-names></name>
<name><surname>Filippo</surname>
<given-names>D. De</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1925</fpage>
<lpage>1927</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of 7,15,17,19-tetraethoxy-2,3,4,5,10,11,12,13-octathiatricyclo[12,2,2,2&lt;sup&gt;6, 9&lt;/sup&gt;]eicosa-6,8,14,16,17,19-hexaene, a sulphur analogue of the paracyclophanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001928</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ricci jun. </surname>
<given-names>John S.</given-names></name>
<name><surname>Bernal</surname>
<given-names>Ivan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1928</fpage>
<lpage>1932</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001928">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001928">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 isomerisation of gaseous C&lt;sub&gt;3&lt;/sub&gt;H&lt;sub&gt;8&lt;/sub&gt;N&lt;sup&gt;+&lt;/sup&gt; metastable ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001933</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Uccella</surname>
<given-names>N. A.</given-names></name>
<name><surname>Howe</surname>
<given-names>I.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1933</fpage>
<lpage>1939</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001933">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001933">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;X&lt;/i&gt;-ray crystal structure determination of the more laevorotatory diastereoisomer of 2′-&lt;i&gt;O&lt;/i&gt;-tetrahydropyranyladenosine. Correlation of physical properties of tetrahydropyranyl ethers with absolute configuration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001940</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kennard</surname>
<given-names>Olga</given-names></name>
<name><surname>Motherwell</surname>
<given-names>W. D. S.</given-names></name>
<name><surname>Coppola</surname>
<given-names>J. C.</given-names></name>
<name><surname>Griffin</surname>
<given-names>B. E.</given-names></name>
<name><surname>Reese</surname>
<given-names>C. B.</given-names></name>
<name><surname>Larson</surname>
<given-names>Allen C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1940</fpage>
<lpage>1946</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001940">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001940">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 resonance study of some reactions involving silyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001947</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowles</surname>
<given-names>A. J.</given-names></name>
<name><surname>Hudson</surname>
<given-names>A.</given-names></name>
<name><surname>Jackson</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1947</fpage>
<lpage>1949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001947">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001947">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Brønsted coefficient for the nucleophilic attack of hydroxamate ions on di-isopropyl phosphorochloridate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001950</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Weinberger</surname>
<given-names>M. A.</given-names></name>
<name><surname>Greenhalgh</surname>
<given-names>R.</given-names></name>
<name><surname>Lutley</surname>
<given-names>Miss P. M.</given-names></name>
<name><surname>Gibson</surname>
<given-names>N. C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1950</fpage>
<lpage>1952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001950">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001950">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>O–H stretching frequencies in bicyclo[2,2,1]heptan-2-ols: measurement of repulsion between aromatic &lt;i&gt;π&lt;/i&gt;- and oxygen lone pair-type orbitals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001952</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>R.</given-names></name>
<name><surname>Dyall</surname>
<given-names>L. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1952</fpage>
<lpage>1957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001952">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001952">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Adsorption effects in the polarographic behaviour of ω-diazoacetophenones in aqueous buffer solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001957</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailes</surname>
<given-names>M.</given-names></name>
<name><surname>Leveson</surname>
<given-names>L. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1957</fpage>
<lpage>1961</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001957">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001957">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transmission of substituent effects in pyridines. Part IV. Alkaline hydrolysis of methyl diazinecarboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001962</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Deady</surname>
<given-names>L. W.</given-names></name>
<name><surname>Foskey</surname>
<given-names>D. J.</given-names></name>
<name><surname>Shanks</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1962</fpage>
<lpage>1963</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001962">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001962">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 effects in the hydrolysis of formaldehyde methyl aryl acetals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001963</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capon</surname>
<given-names>B.</given-names></name>
<name><surname>Anderson</surname>
<given-names>E.</given-names></name>
<name><surname>Anderson</surname>
<given-names>N. S.</given-names></name>
<name><surname>Dahm</surname>
<given-names>R. H.</given-names></name>
<name><surname>Smith</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1963</fpage>
<lpage>1966</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001963">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001963">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrolysis of phosphinic esters: general-base catalysis by imidazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001967</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>Andrew</given-names></name>
<name><surname>Naylor</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1967</fpage>
<lpage>1972</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001967">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001967">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;2(P) mechanism in the phosphorylation of alkaline phosphatase by substrates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001973</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>Andrew</given-names></name>
<name><surname>Naylor</surname>
<given-names>Richard A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1973</fpage>
<lpage>1979</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001973">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001973">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 gas phase reactions of &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-2,3-epoxybutane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001980</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>M. C.</given-names></name>
<name><surname>Parker</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1980</fpage>
<lpage>1988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001980">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001980">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 organophosphorus compounds. Part XXVII. Reactions of alkyl hydrogen alkylphosphonates with &lt;i&gt;p&lt;/i&gt;-nitrobenzonitrile oxide: anchimerically assisted P–O fission in acidic hydrolysis of the resulting α-hydroxyimino-&lt;i&gt;p&lt;/i&gt;-nitrobenzyl alkylphosphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001988</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Challis</surname>
<given-names>(Mrs) J. A.</given-names></name>
<name><surname>Eastlick</surname>
<given-names>D. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1988</fpage>
<lpage>1995</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001988">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001988">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylarylnitrosamines. Part IV. Aryne participation in decompositions of &lt;i&gt;N&lt;/i&gt;-nitrosoacetanilide and its &lt;i&gt;m&lt;/i&gt;- and &lt;i&gt;p&lt;/i&gt;-t-butyl-, &lt;i&gt;o&lt;/i&gt;-, &lt;i&gt;m&lt;/i&gt;-, and &lt;i&gt;p&lt;/i&gt;-chloro-derivatives in benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710001996</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brydon</surname>
<given-names>D. L.</given-names></name>
<name><surname>Cadogan</surname>
<given-names>J. I. G.</given-names></name>
<name><surname>Cook</surname>
<given-names>J.</given-names></name>
<name><surname>Harger</surname>
<given-names>M. J. P.</given-names></name>
<name><surname>Sharp</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>1996</fpage>
<lpage>2006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710001996">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710001996">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical production of the electrophilic cyano-radical: homolytic aromatic cyanation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002006</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spagnolo</surname>
<given-names>P.</given-names></name>
<name><surname>Testaferri</surname>
<given-names>L.</given-names></name>
<name><surname>Tiecco</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2006</fpage>
<lpage>2008</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;X&lt;/i&gt;-ray evidence for contrasting stereochemistry in related diene addition products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002009</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pointer</surname>
<given-names>D. J.</given-names></name>
<name><surname>Wilford</surname>
<given-names>J. B.</given-names></name>
<name><surname>Hodder</surname>
<given-names>O. J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2009</fpage>
<lpage>2014</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002009">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002009">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Magnetic shielding by the azo-group. A nuclear magnetic resonance study of phenylazoalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002014</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ege</surname>
<given-names>Seyhan N.</given-names></name>
<name><surname>Sharp</surname>
<given-names>Robert R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2014</fpage>
<lpage>2020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002014">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002014">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structure of fusicoccin A &lt;i&gt;p&lt;/i&gt;-iodobenzenesulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002021</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brufani</surname>
<given-names>M.</given-names></name>
<name><surname>Cerrini</surname>
<given-names>S.</given-names></name>
<name><surname>Fedeli</surname>
<given-names>W.</given-names></name>
<name><surname>Vaciago</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2021</fpage>
<lpage>2026</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002021">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002021">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Comments on the mechanism of one-electron oxidation of phenols: a fresh interpretation of oxidative coupling reactions of plant phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2026</fpage>
<lpage>2029</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ring inversion of 1,3,5-trithian</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002030</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2030</fpage>
<lpage>2030</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 catalysed thermal decomposition of organic acids. Part I. The catalysed decomposition of cyclohexanecarboxylic acid by hydrogen bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002031</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahonkhai</surname>
<given-names>S. I.</given-names></name>
<name><surname>Emovon</surname>
<given-names>E. U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2031</fpage>
<lpage>2033</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002031">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002031">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ultraviolet absorption and protonation equilibria of amino- and nitro-substituted pyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002034</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellobono</surname>
<given-names>I. R.</given-names></name>
<name><surname>Favini</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2034</fpage>
<lpage>2037</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002034">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002034">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 and Raman spectra of some thioacetals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002037</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wladislaw</surname>
<given-names>B.</given-names></name>
<name><surname>Olivato</surname>
<given-names>P. R.</given-names></name>
<name><surname>Sala</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2037</fpage>
<lpage>2040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002037">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002037">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Search for general acid catalysis in the reduction and racemization of sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002041</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landini</surname>
<given-names>D.</given-names></name>
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
<name><surname>Quintily</surname>
<given-names>U.</given-names></name>
<name><surname>Scorrano</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2041</fpage>
<lpage>2044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 infrared study of solvent effects on the carbonyl stretching bands of some androgen esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>James</surname>
<given-names>K. C.</given-names></name>
<name><surname>Noyce</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2045</fpage>
<lpage>2048</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sign determination of geminal and long-range cumulenic coupling constants</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002049</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>M. L.</given-names></name>
<name><surname>Lefevre</surname>
<given-names>F.</given-names></name>
<name><surname>Mantione</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2049</fpage>
<lpage>2050</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002049">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002049">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 keten. Part II. The thermodynamics of the gas-phase equilibrium: acetic acid + keten ⇌ acetic anhydride
</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002050</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Davies</surname>
<given-names>H. H.</given-names></name>
<name><surname>Speis</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2050</fpage>
<lpage>2052</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002050">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002050">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cathodic reduction of the tropylium cation in methylene dichloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002052</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Plesch</surname>
<given-names>P. H.</given-names></name>
<name><surname>Stasko</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2052</fpage>
<lpage>2053</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002052">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002052">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 benzidine and semidine rearrangements. Part XXIII. Kinetics and products of acid-catalysed conversion of 4-phenyl-; 4-nitro-; 2,2′-diphenyl-; and 4,4′-difluoro-substituted hydrazobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002054</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Cooper</surname>
<given-names>Anthony</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2054</fpage>
<lpage>2057</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002054">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002054">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 benzidine and semidine rearrangements. Part XXIV. Photochemical decomposition of hydrazoarenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002057</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Cooper</surname>
<given-names>Anthony</given-names></name>
<name><surname>Pearce</surname>
<given-names>D. A.</given-names></name>
<name><surname>Thomas</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2057</fpage>
<lpage>2060</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002057">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002057">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;E&lt;/i&gt;1cB eliminations. Part V. Two types of &lt;i&gt;E&lt;/i&gt;1cB reaction in the amine-catalysed elimination of HCN from 2,6-dimethyl-4-(ααββ-tetracyanoethyl)aniline in chloroform</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002060</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
<name><surname>Shohamy</surname>
<given-names>Esther</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2060</fpage>
<lpage>2068</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002060">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002060">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structural dependence of the inductive effect. Part I. The calculation of geminal substituent effects upon fluorine-19 chemical shifts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Phillips</surname>
<given-names>L.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2068</fpage>
<lpage>2074</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 structural dependence of the inductive effect. Part II. The shielding of fluorine bonded to octahedral tin(IV) complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Phillips</surname>
<given-names>L.</given-names></name>
<name><surname>Wray</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2074</fpage>
<lpage>2076</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Synthesis and emission characteristics of some fluorescent derivatives of 2-(2-quinolyl)thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002077</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>R. E.</given-names></name>
<name><surname>Speakman</surname>
<given-names>P. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2077</fpage>
<lpage>2081</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002077">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002077">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 modification to the ferrioxalate actinometer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002081</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurien</surname>
<given-names>K. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2081</fpage>
<lpage>2082</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002081">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002081">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Transmission of electronic effects in organosilanols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002083</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>Glyn I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2083</fpage>
<lpage>2086</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 in the gas phase. Part I. Reaction of the helium tritiide molecular ion with halogenobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002086</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cacace</surname>
<given-names>Fulvio</given-names></name>
<name><surname>Perez</surname>
<given-names>Giorgio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2086</fpage>
<lpage>2089</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002086">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002086">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 in the gas phase. Part II. Reactions of the helium tritiide ion with anisole, t-butylbenzene, and ααα-trifluorotoluene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002089</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cacace</surname>
<given-names>Fulvio</given-names></name>
<name><surname>Cipollini</surname>
<given-names>Romano</given-names></name>
<name><surname>Ciranni</surname>
<given-names>Giovanna</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2089</fpage>
<lpage>2092</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002089">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002089">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 proton magnetic resonance spectra of polynuclear heterocycles. Part III. Electronic spectra and high-resolution proton magnetic resonance of acenaphtho[1,2-&lt;i&gt;b&lt;/i&gt;]thiophen and acenaphtho[1,2-&lt;i&gt;c&lt;/i&gt;]thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002092</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartle</surname>
<given-names>K. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. W.</given-names></name>
<name><surname>Matthews</surname>
<given-names>R. S.</given-names></name>
<name><surname>Birch</surname>
<given-names>A.</given-names></name>
<name><surname>Crombie</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2092</fpage>
<lpage>2096</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002092">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002092">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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-cycloadditions of benzonitrile &lt;i&gt;N&lt;/i&gt;-oxides to thiobenzophenones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battaglia</surname>
<given-names>A.</given-names></name>
<name><surname>Dondoni</surname>
<given-names>A.</given-names></name>
<name><surname>Maccagnani</surname>
<given-names>G.</given-names></name>
<name><surname>Mazzanti</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2096</fpage>
<lpage>2100</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Conformations of some substituted styrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002100</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Britton</surname>
<given-names>P. L.</given-names></name>
<name><surname>Cheng</surname>
<given-names>C. L.</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2100</fpage>
<lpage>2103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002100">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002100">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 conformation of &lt;i&gt;N&lt;/i&gt;-phenylaziridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002104</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armstrong</surname>
<given-names>R. S.</given-names></name>
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Stootman</surname>
<given-names>(Mrs.) H. J.</given-names></name>
<name><surname>Lüttke</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2104</fpage>
<lpage>2107</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002104">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002104">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 reaction of &lt;i&gt;p&lt;/i&gt;-substituted nitrosobenzenes with &lt;i&gt;N&lt;/i&gt;-alkyl-&lt;i&gt;N&lt;/i&gt;-arylhydroxylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002107</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knight</surname>
<given-names>G. T.</given-names></name>
<name><surname>Loadman</surname>
<given-names>M. J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2107</fpage>
<lpage>2112</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002107">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002107">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 comparison of substituent effects on the proton and carbon basicities of thiophenoxide ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002112</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2112</fpage>
<lpage>2116</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidation of α-glycols by periodic acid. Part IX. Propane-1,2-diol: kinetics of formation of the intermediate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002117</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buist</surname>
<given-names>G. J.</given-names></name>
<name><surname>Bunton</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2117</fpage>
<lpage>2128</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002117">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002117">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 oxidation of α-glycols by periodic acid. Part X. The oxidation of pinacol, and a general discussion of the stability of periodate esters and their role in the mechanism of oxidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buist</surname>
<given-names>G. J.</given-names></name>
<name><surname>Bunton</surname>
<given-names>C. A.</given-names></name>
<name><surname>Hipperson</surname>
<given-names>W. C. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2128</fpage>
<lpage>2142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XLVII. Effects of 10-substituents on the rates of detritiation at the 9-position of phenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Fischer</surname>
<given-names>A.</given-names></name>
<name><surname>Killpack</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2142</fpage>
<lpage>2145</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of tropan-3-yl ethers. Part I. Synthesis of tropan-3-yl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002145</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kraiss</surname>
<given-names>G.</given-names></name>
<name><surname>Scheiber</surname>
<given-names>P.</given-names></name>
<name><surname>Nádor</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2145</fpage>
<lpage>2149</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002145">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002145">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of tropan-3-yl ethers. Part II. Configuration and conformation of phenyl tropan-3-yl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002149</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scheiber</surname>
<given-names>P.</given-names></name>
<name><surname>Kraiss</surname>
<given-names>G.</given-names></name>
<name><surname>Nádor</surname>
<given-names>K.</given-names></name>
<name><surname>Neszmélyi</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2149</fpage>
<lpage>2153</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002149">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002149">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemistry of tropan-3-yl ethers. Part III. Kinetic properties of tropan-3α-yl methanesulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002154</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Scheiber</surname>
<given-names>P.</given-names></name>
<name><surname>Kraiss</surname>
<given-names>G.</given-names></name>
<name><surname>Nádor</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2154</fpage>
<lpage>2156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002154">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002154">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 studies on the alcoholysis of &lt;i&gt;N&lt;/i&gt;-sulphinylaniline, using copper(II) chloride as catalyst</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>N. C.</given-names></name>
<name><surname>Glass</surname>
<given-names>W. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2156</fpage>
<lpage>2159</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 maytoline methiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002159</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryan</surname>
<given-names>Robert F.</given-names></name>
<name><surname>Smith</surname>
<given-names>Roger M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2159</fpage>
<lpage>2163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002159">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002159">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 organometallic compounds containing silicon. Part IV.&lt;sup&gt;1&lt;i&gt;a&lt;/i&gt;&lt;/sup&gt; Reactions of dimethylphenyl-, methyldiphenyl- and triphenylsilyl-lithium with 9-methylfluorene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Hamid</surname>
<given-names>M. A.</given-names></name>
<name><surname>Rees</surname>
<given-names>N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2164</fpage>
<lpage>2167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 2-chlorotropone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002167</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Watkin</surname>
<given-names>D. J.</given-names></name>
<name><surname>Hamor</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2167</fpage>
<lpage>2170</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002167">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002167">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 organometallic reactions. Part V. Homolytic bimolecular substitution at boron by the triplet state of ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002171</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>
<name><surname>Scaiano</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2171</fpage>
<lpage>2176</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002171">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002171">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 macrocyclic compounds. Part LXXXIII. A quantitative study of the conformational mobility of [18]annulene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002177</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilles</surname>
<given-names>J.-M.</given-names></name>
<name><surname>Oth</surname>
<given-names>J. F. M.</given-names></name>
<name><surname>Sondheimer</surname>
<given-names>F.</given-names></name>
<name><surname>Woo</surname>
<given-names>E. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2177</fpage>
<lpage>2186</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002177">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002177">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 at two-co-ordinate sulphur. Brønsted relationships with nitrogen nucleophiles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002187</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ciuffarin</surname>
<given-names>Ennio</given-names></name>
<name><surname>Senatore</surname>
<given-names>Lucio</given-names></name>
<name><surname>Isola</surname>
<given-names>Mauro</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2187</fpage>
<lpage>2190</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002187">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002187">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 at two-co-ordinate sulphur. Effect of the leaving group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002191</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Senatore</surname>
<given-names>Lucio</given-names></name>
<name><surname>Ciuffarin</surname>
<given-names>Ennio</given-names></name>
<name><surname>Sagramora</surname>
<given-names>Laura</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2191</fpage>
<lpage>2193</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002191">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002191">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 charge-transfer complexes of 1,4-naphthoquinone acceptors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002194</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2194</fpage>
<lpage>2197</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002194">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002194">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 bromination of heterocyclic hydrazones. &lt;i&gt;syn&lt;/i&gt;–&lt;i&gt;anti&lt;/i&gt;-Isomerisation of 5-(arymethylenehydrazino)-1- and -2-benzyltetrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002198</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tobin</surname>
<given-names>J. C.</given-names></name>
<name><surname>Hegarty</surname>
<given-names>A. F.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2198</fpage>
<lpage>2202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002198">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002198">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 and nuclear magnetic resonance study of the acetic anhydride–sulphuric acid system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clemett</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2202</fpage>
<lpage>2205</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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-conventional paths in electrophilic aromatic reactions. Part IX. Chlorination of hexaethylbenzene and some of its cyclic analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002206</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Illuminati</surname>
<given-names>G.</given-names></name>
<name><surname>Mandolini</surname>
<given-names>L.</given-names></name>
<name><surname>Arnett</surname>
<given-names>E. M.</given-names></name>
<name><surname>Smoyer</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2206</fpage>
<lpage>2208</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002206">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002206">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 halogenobenzofurazans and halogenonitrobenzofurazans with nucleophiles. Part I. Methoxy-dehalogenation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002209</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Monte</surname>
<given-names>D. Dal</given-names></name>
<name><surname>Sandri</surname>
<given-names>E.</given-names></name>
<name><surname>Nunno</surname>
<given-names>L. Di</given-names></name>
<name><surname>Florio</surname>
<given-names>S.</given-names></name>
<name><surname>Todesco</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2209</fpage>
<lpage>2213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002209">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002209">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XIII. The formation and hydrolysis of simple potassium pyrimidinesulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002214</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Hoskins</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2214</fpage>
<lpage>2217</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002214">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002214">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XI. A boat-chair bicyclo[3,3,1]nonane: crystal structure analysis of 9-benzoyl-3α-bromo-9-azabicyclo[3,3,1]-nonan-2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002218</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cradwick</surname>
<given-names>P. D.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2218</fpage>
<lpage>2221</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002218">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002218">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effect of some electron-withdrawing substituents from the &lt;i&gt;meta&lt;/i&gt;- and &lt;i&gt;para&lt;/i&gt;-positions in aromatic nucleophilic replacement reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002221</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hirst</surname>
<given-names>J.</given-names></name>
<name><surname>Una</surname>
<given-names>S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2221</fpage>
<lpage>2224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002221">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002221">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 pseudoaromatic compounds. Part IV. Normal substitutions of 2-substituted tropones by secondary or tertiary amines; abnormal behaviour of 2-fluorotropone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002224</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pietra</surname>
<given-names>Francesco</given-names></name>
<name><surname>Cima</surname>
<given-names>Francesco Del</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2224</fpage>
<lpage>2230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002224">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002224">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 ketones and esters in basic solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gersmann</surname>
<given-names>H. R.</given-names></name>
<name><surname>Bickel</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2230</fpage>
<lpage>2237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidation of anthracene with cerium(IV) ammonium nitrate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002238</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rindone</surname>
<given-names>B.</given-names></name>
<name><surname>Scolastico</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2238</fpage>
<lpage>2241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002238">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002238">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 stereochemistry of organometallic compounds. Part XI. The variable temperature nuclear magnetic resonance spectra of di-µ-chloro-bis-[(α,1,2-&lt;i&gt;trihapto&lt;/i&gt;-3,3,5,5-tetramethylmethylenecyclohexane)-palladium(II)]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alexander</surname>
<given-names>C. W.</given-names></name>
<name><surname>Jackson</surname>
<given-names>W. R.</given-names></name>
<name><surname>Jennings</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2241</fpage>
<lpage>2243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Effect of fluorine substitution on the molecular core binding energies of some binuclear aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002243</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>D. T.</given-names></name>
<name><surname>Kilcast</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2243</fpage>
<lpage>2247</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002243">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002243">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 and kinetics in the isomerisation of &lt;i&gt;o&lt;/i&gt;-formylbenzoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002247</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Cox</surname>
<given-names>B. G.</given-names></name>
<name><surname>Timimi</surname>
<given-names>B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2247</fpage>
<lpage>2250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002247">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002247">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of solvent effects on the kinetics of hydrogen abstraction from 2,4,6-tri-t-butylphenol by 2,2-diphenyl-1-picrylhydrazyl free radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002251</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dearden</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2251</fpage>
<lpage>2254</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002251">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002251">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemical reactions of aliphatic aldehydes in solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002254</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coyle</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2254</fpage>
<lpage>2256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002254">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002254">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cycloadditions of simple allyl cations to conjugated dienes. Optimization and scope of the reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002257</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hoffmann</surname>
<given-names>H. M. R.</given-names></name>
<name><surname>Kernaghan</surname>
<given-names>G. F. P.</given-names></name>
<name><surname>Greenwood</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2257</fpage>
<lpage>2261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002257">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002257">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XLVIII. Hydrogen exchange in the methyl groups of 2-methyl-, 3-methyl-, and 2,3-dimethyl-benzo[&lt;i&gt;b&lt;/i&gt;]thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Wright</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2262</fpage>
<lpage>2264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic iodination by iodine and nitric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>Anthony R.</given-names></name>
<name><surname>Sanderson</surname>
<given-names>Anthony P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2264</fpage>
<lpage>2268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Second-&lt;i&gt;versus&lt;/i&gt; third-order kinetics in the base-catalysed halogenation of di-isopropyl ketone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lii</surname>
<given-names>Ruey-Rong</given-names></name>
<name><surname>Miller</surname>
<given-names>Sidney I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2269</fpage>
<lpage>2270</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Inverse kinetic dependence on hydroxide in the reaction of hypochlorite with nitroethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002271</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lii</surname>
<given-names>Ruey-Rong</given-names></name>
<name><surname>Miller</surname>
<given-names>Sidney I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2271</fpage>
<lpage>2272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002271">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002271">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deuterium solvent isotope effects in methanol solution. Part II. The general acid-catalysed reaction of cyanoketen dimethyl acetal with solvent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Grist</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2272</fpage>
<lpage>2281</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deuterium solvent isotope effects in methanol solution. Part III. Proton transfer from 2-nitropropane and from 3-methyl-1-phenylbutyl phenyl ketone to methoxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002282</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Grist</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2282</fpage>
<lpage>2285</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002282">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002282">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Deuterium solvent isotope effects in methanol solution. Part IV. The solvolysis of acetic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002285</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Grist</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2285</fpage>
<lpage>2286</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002285">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002285">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 quaternization and conformational analysis of some substituted &lt;i&gt;NN&lt;/i&gt;-dimethylcyclohexylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002287</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ramalingam</surname>
<given-names>K.</given-names></name>
<name><surname>Balasubramanian</surname>
<given-names>(the late) M.</given-names></name>
<name><surname>Baliah</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2287</fpage>
<lpage>2290</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002287">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002287">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 conformation and electronic structure of azomethines. Part IV. The electric dipole moments of &lt;i&gt;para&lt;/i&gt;-substituted &lt;i&gt;N&lt;/i&gt;-benzylidenemethylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002290</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pitea</surname>
<given-names>D.</given-names></name>
<name><surname>Grasso</surname>
<given-names>D.</given-names></name>
<name><surname>Favini</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2290</fpage>
<lpage>2293</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002290">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002290">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pressure effects and quantum yields in the photolysis of ethylene and propene at 185 nm</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002293</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Borrell</surname>
<given-names>Peter</given-names></name>
<name><surname>Cervenka</surname>
<given-names>A.</given-names></name>
<name><surname>Turner</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2293</fpage>
<lpage>2298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002293">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002293">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the transalkylation between some alkyl heterocyclic ethers and thiophenol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002299</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dembech</surname>
<given-names>P.</given-names></name>
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
<name><surname>Seconi</surname>
<given-names>G.</given-names></name>
<name><surname>Vivarelli</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2299</fpage>
<lpage>2301</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002299">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002299">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heteroaromatic rings as substituents. Part II. Evaluation of the electrophilic substituent constants for 2- and 3-thienyl groups from the solvolysis of 2-chloro-2-(thienylphenyl)propanes in 90% aqueous acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fringuelli</surname>
<given-names>Francesco</given-names></name>
<name><surname>Marino</surname>
<given-names>Gianlorenzo</given-names></name>
<name><surname>Taticchi</surname>
<given-names>Aldo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2302</fpage>
<lpage>2303</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heteroaromatic rings as substituents. Part III. The electronic effects of the 2-furyl group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002304</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fringuelli</surname>
<given-names>Francesco</given-names></name>
<name><surname>Marino</surname>
<given-names>Gianlorenzo</given-names></name>
<name><surname>Taticchi</surname>
<given-names>Aldo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2304</fpage>
<lpage>2306</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002304">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002304">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 &lt;i&gt;syn&lt;/i&gt;-2,11-dithia-9,18-dimethyl[3,3]metacyclophane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002307</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>Betty R.</given-names></name>
<name><surname>Bernal</surname>
<given-names>Ivan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2307</fpage>
<lpage>2313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002307">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002307">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the gaseous carbonium ions from the decay of [1,2-&lt;sup&gt;3&lt;/sup&gt;H&lt;sub&gt;2&lt;/sub&gt;]-cyclopentane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002313</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Babérnics</surname>
<given-names>L.</given-names></name>
<name><surname>Cacace</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2313</fpage>
<lpage>2316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Calculation of rate constants for gas-phase bimolecular halogen atom transfer reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Previtali</surname>
<given-names>C. M.</given-names></name>
<name><surname>Scainao</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2317</fpage>
<lpage>2320</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 properties of hydrochloric acid in dimethylformamide–water mixtures at different temperatures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002320</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roy</surname>
<given-names>Rabindra N.</given-names></name>
<name><surname>Vernon</surname>
<given-names>William</given-names></name>
<name><surname>Bothwell</surname>
<given-names>Alfred L. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2320</fpage>
<lpage>2322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002320">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002320">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 IX. Trimethylammonio- and dimethylamino-&lt;i&gt;N&lt;/i&gt;-methyl-derivatives of quinoline, isoquinoline, cinnoline, phthalazine, quinazoline, and quinoxaline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Young</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2323</fpage>
<lpage>2329</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 absorption and isomerism of 3-aminocrotonic esters. Part I. 3-(Alkylamino)crotonic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002330</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sánchez</surname>
<given-names>A. Gómez</given-names></name>
<name><surname>Valle</surname>
<given-names>A. M.</given-names></name>
<name><surname>Bellanato</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2330</fpage>
<lpage>2335</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002330">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002330">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nucleophilic addition of some aromatic thiols to aryl vinyl sulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002335</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maria</surname>
<given-names>P. De</given-names></name>
<name><surname>Fini</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2335</fpage>
<lpage>2338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002335">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002335">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 pyridines. Part XII. The stabilisation of hydroxy-forms by intramolecular hydrogen-bonding</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bean</surname>
<given-names>G. P.</given-names></name>
<name><surname>Cook</surname>
<given-names>M. J.</given-names></name>
<name><surname>Dand</surname>
<given-names>T. M.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Lea</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2339</fpage>
<lpage>2344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 azines. Part V. Cinnolin-3(2&lt;i&gt;H&lt;/i&gt;)-one and 3- and 4-aminocinnoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Fletcher</surname>
<given-names>I. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2344</fpage>
<lpage>2350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 heteroaromatic compounds with five-membered rings. Part XII. The imidazole 3-oxide &lt;i&gt;versus&lt;/i&gt; 3-hydroxy[3H]imidazole equilibrium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002350</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chua</surname>
<given-names>S. O.</given-names></name>
<name><surname>Cook</surname>
<given-names>M. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2350</fpage>
<lpage>2355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002350">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002350">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 heteroaromatic compounds with five-membered rings. Part XIII. The tautomeric structure of 1-methyl-5-methyl-aminotetrazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bianchi</surname>
<given-names>G.</given-names></name>
<name><surname>Boulton</surname>
<given-names>A. J.</given-names></name>
<name><surname>Fletcher</surname>
<given-names>I. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2355</fpage>
<lpage>2358</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 XLI. &lt;i&gt;cis&lt;/i&gt;-&lt;i&gt;trans&lt;/i&gt;-Equilibria of 4-thia- and 4-oxa-analogues of 2,6-dimethylcyclohexanone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002358</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>M. D.</given-names></name>
<name><surname>Cook</surname>
<given-names>M. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2358</fpage>
<lpage>2363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002358">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002358">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the electrophilic substitution of heteroaromatic compounds. Part XXV. The acid-catalysed hydrogen-exchange of some 2-aminopyridine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002363</article-id><contrib-group><contrib contrib-type="author">
<name><surname>El-Anani</surname>
<given-names>A.</given-names></name>
<name><surname>Jones</surname>
<given-names>P. E.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2363</fpage>
<lpage>2365</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002363">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002363">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mechanism of the electrophilic substitution of heteroaromatic compounds. Part XXVII. The nitration and hydrogen exchange of 1,3,5-trimethylpyrazole, 3,5-dimethylisoxazole, and 3,5-dimethylisothiazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002365</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burton</surname>
<given-names>A. G.</given-names></name>
<name><surname>Forsythe</surname>
<given-names>P. 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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2365</fpage>
<lpage>2371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002365">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002365">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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;X&lt;/i&gt;-ray structural analysis of two isomeric modifications of 1,3-diphenyl-2-(phenylazo)propene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002372</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Serantoni</surname>
<given-names>E. Foresti</given-names></name>
<name><surname>Sanseverino</surname>
<given-names>L. Riva di</given-names></name>
<name><surname>Rosini</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2372</fpage>
<lpage>2374</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002372">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002372">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 of phenylacetic acid and three substituted phenylacetic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duer</surname>
<given-names>Wayne C.</given-names></name>
<name><surname>Robinson</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2375</fpage>
<lpage>2375</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular reactions of nitro-olefin–cyclohexane-1,3-dione Michael adducts. Crystal structure of 3-(4-bromophenyl)-6,7-dihydro-2-hydroxyiminobenzofuran-4(5&lt;i&gt;H&lt;/i&gt;)-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002376</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>Gerald B.</given-names></name>
<name><surname>Moore</surname>
<given-names>Donald W.</given-names></name>
<name><surname>Nielsen</surname>
<given-names>Arnold T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2376</fpage>
<lpage>2382</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002376">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002376">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Determination of electrophilic aromatic reactivities &lt;i&gt;via&lt;/i&gt; pyrolysis of 1-arylethyl acetates. Part VII. The total reactivity of quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002382</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2382</fpage>
<lpage>2387</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002382">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 nature of cyclopropane. Its interaction as a solvent with polar solutes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002388</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2388</fpage>
<lpage>2390</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002388">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002388">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 mass spectral fragmentation of some phenoxaphosphinic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002391</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Granoth</surname>
<given-names>I.</given-names></name>
<name><surname>Levy</surname>
<given-names>Jack B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2391</fpage>
<lpage>2393</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002391">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002391">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 between aromatic nitro-compounds and hydroxylamines in alkaline solution. Part I. Kinetic studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002393</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cowley</surname>
<given-names>D. J.</given-names></name>
<name><surname>Millen</surname>
<given-names>(Miss) M. H.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2393</fpage>
<lpage>2397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002393">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002393">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 between aromatic nitro-compounds and hydroxylamines in alkaline solution. Part II. Product studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002398</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Millen</surname>
<given-names>(Miss) M. H.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2398</fpage>
<lpage>2400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002398">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002398">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrolysis of acylchymotrypsins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>Andrew</given-names></name>
<name><surname>Salvadori</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2401</fpage>
<lpage>2406</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Radical anions of pyridine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002406</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kalyanaraman</surname>
<given-names>V.</given-names></name>
<name><surname>Rao</surname>
<given-names>C. N. R.</given-names></name>
<name><surname>George</surname>
<given-names>M. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2406</fpage>
<lpage>2409</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002406">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002406">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 the rearrangement of 1-&lt;sup&gt;1&lt;/sup&gt; and 2-naphthylsulphamic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002409</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spillane</surname>
<given-names>W. J.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
<name><surname>Goggin</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2409</fpage>
<lpage>2414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002409">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002409">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 glycolaldehyde and glyceraldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002414</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brittain</surname>
<given-names>E. F. H.</given-names></name>
<name><surname>George</surname>
<given-names>W. O.</given-names></name>
<name><surname>Collins</surname>
<given-names>G. C. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2414</fpage>
<lpage>2416</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002414">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002414">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 spectrum of the diphenylfulvene radical-anion: a new triarylmethyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002416</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Camaggi</surname>
<given-names>C. M.</given-names></name>
<name><surname>Perkins</surname>
<given-names>M. J.</given-names></name>
<name><surname>Ward</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2416</fpage>
<lpage>2417</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002416">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002416">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 on circular dichroism of α-phenylethylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002418</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gottarelli</surname>
<given-names>G.</given-names></name>
<name><surname>Samorì</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2418</fpage>
<lpage>2423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002418">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002418">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Pteridine studies. Part XLII. Addition reactions between alcohols and pteridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002423</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Mizuno</surname>
<given-names>Hatsuhiko</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2423</fpage>
<lpage>2427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002423">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002423">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Frequency shifts in the electronic spectra of some methylated naphthalenes and anthracenes and their radical ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002427</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dodd</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2427</fpage>
<lpage>2430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002427">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002427">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular screening effects on nuclear magnetic resonance chemical shifts. Part V. The fluorine-19 magnetic resonance spectra of some bridgehead substituted fluorobicyclo[2,2,1]heptenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002430</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Homer</surname>
<given-names>J.</given-names></name>
<name><surname>Callaghan</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2430</fpage>
<lpage>2433</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002430">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002430">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 quadrupole resonance of substituted anilines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002433</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Krause</surname>
<given-names>L.</given-names></name>
<name><surname>Whitehead</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2433</fpage>
<lpage>2438</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002433">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002433">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Radical addition reactions of alkenylsilanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002439</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jarvie</surname>
<given-names>A. W. P.</given-names></name>
<name><surname>Rowley</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2439</fpage>
<lpage>2442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002439">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002439">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part VIII. Isomer ratios and assignment of mechanism in aromatic nitration. &lt;i&gt;o&lt;/i&gt;-xylene and biphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coombes</surname>
<given-names>R. G.</given-names></name>
<name><surname>Russell</surname>
<given-names>L. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2443</fpage>
<lpage>2447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part IX. The kinetics of nitration of benzene and some methylbenzenes in aqueous acetic acid and in acetic anhydride, with observations on limiting rates of nitration and on M.O.-theoretical treatments of nitration rates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002447</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>S. R.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Thompson</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2447</fpage>
<lpage>2453</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002447">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002447">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part X. The kinetics and mechanism of nitration of some anilides and aromatic ethers in sulphuric acid and in acetic anhydride, with particular reference to the existence of a special mechanism for &lt;i&gt;ortho&lt;/i&gt;-nitration in the latter medium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>S. R.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2454</fpage>
<lpage>2461</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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 aromatic substitution. Part XI. The kinetics and mechanism of the nitration of reactive aromatic substrates in acetic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002461</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>S. R.</given-names></name>
<name><surname>Hoggett</surname>
<given-names>J. G.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Thompson</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2461</fpage>
<lpage>2469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002461">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002461">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Ultrasonic relaxation and ring inversion associated with chair to chair and twist-boat to chair conformational changes in 1,3-dioxans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eccleston</surname>
<given-names>G.</given-names></name>
<name><surname>Wyn-Jones</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2469</fpage>
<lpage>2474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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, 1971</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002475</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2475</fpage>
<lpage>2494</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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, 1971</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29710002495</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>2495</fpage>
<lpage>2518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29710002495">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J29710002495">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: 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. Section B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2971000X001</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>X001</fpage>
<lpage>X002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2971000X001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J2971000X001">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>Journal of the Chemical Society</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2971000X003</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>1971</year></pub-date>
<volume>1971</volume>
<issue />
<fpage>X003</fpage>
<lpage>X015</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2971000X003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1971/J2/J2971000X003">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
</articles>
