<?xml version="1.0" encoding="utf-8"?>
<articles xmlns:xlink="http://www.w3.org/1999/xlink">
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</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/JR95600FP001</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR95600FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR95600FP001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</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/JR95600FP003</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR95600FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR95600FP003">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</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/JR95600FP005</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>P005</fpage>
<lpage>P006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR95600FP005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR95600FP005">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</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/JR95600FP007</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>P007</fpage>
<lpage>P008</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR95600FP007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR95600FP007">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1. The reaction of &lt;i&gt;o&lt;/i&gt;-di-iodobenzene with magnesium, lithium, and &lt;i&gt;n&lt;/i&gt;-butyl-lithium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heaney</surname>
<given-names>Harry</given-names></name>
<name><surname>Mann</surname>
<given-names>Frederick G.</given-names></name>
<name><surname>Millar</surname>
<given-names>Ian T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1</fpage>
<lpage>5</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>2. The effect of solvents on the molecular complexities of tantalum &lt;i&gt;n&lt;/i&gt;-alkoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000005</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
<name><surname>Whitley</surname>
<given-names>(Miss) Alice</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>5</fpage>
<lpage>7</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000005">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>3. The absorption spectra and stability of complex ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>R. J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>8</fpage>
<lpage>15</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>4. Thermochromism of compounds containing the thiocarbonyl and disulphide functions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brand</surname>
<given-names>J. C. D.</given-names></name>
<name><surname>Davidson</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>15</fpage>
<lpage>22</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>5. Sedimentation potentials. Part I. The measurement of sedimentation potentials in some aqueous and non-aqueous media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000022</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elton</surname>
<given-names>G. A. H.</given-names></name>
<name><surname>Peace</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>22</fpage>
<lpage>26</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000022">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000022">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>6. Cinnolines and other heterocyclic types in relation to the chemotherapy of trypanosomiasis. Part XI. Some reactions of simple quinoxaline derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>C. M.</given-names></name>
<name><surname>Brown</surname>
<given-names>C. W.</given-names></name>
<name><surname>Simpson</surname>
<given-names>(the late) J. C. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>26</fpage>
<lpage>30</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>7. Ionophoresis of carbohydrates. Part III. Behaviour of some amylosaccharides and their reaction with borate ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Newton-Hearn</surname>
<given-names>Miss P. A.</given-names></name>
<name><surname>Stacey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>30</fpage>
<lpage>36</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>8. The kinetics and mechanisms of aromatic halogen substitution. Part II. Partial rate factors for the acid-catalysed bromination of toluene by hypobromous acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Harvey</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>36</fpage>
<lpage>40</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>9. The reaction between &lt;i&gt;tert&lt;/i&gt;.-butyl chloride and sodium thiophenoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000041</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>41</fpage>
<lpage>44</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000041">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000041">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>10. The enzymic synthesis and degradation of starch. Part XX. The disproportionating enzyme (D-enzyme) of the potato</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peat</surname>
<given-names>Stanley</given-names></name>
<name><surname>Whelan</surname>
<given-names>W. J.</given-names></name>
<name><surname>Rees</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>44</fpage>
<lpage>53</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>11. The enzymic synthesis and degradation of starch. Part XXI. The dextrins synthesised by D-enzyme</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000053</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peat</surname>
<given-names>Stanley</given-names></name>
<name><surname>Whelan</surname>
<given-names>W. J.</given-names></name>
<name><surname>Kroll</surname>
<given-names>(the late) G. W. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>53</fpage>
<lpage>55</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000053">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000053">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>12. Infrared spectra and the polymorphism of glycerides. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000055</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>55</fpage>
<lpage>60</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000055">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000055">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>13. Addition of free radicals to unsaturated systems. Part XII. Free-radical and electrophilic attack on fluoro-olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000061</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Osborne</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>61</fpage>
<lpage>71</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000061">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000061">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>14. Studies in hydrogen-bond formation. Part III. The reactivity of amines, amides, and azo-compounds in aqueous and non-aqueous solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000072</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arshid</surname>
<given-names>F. M.</given-names></name>
<name><surname>Giles</surname>
<given-names>C. H.</given-names></name>
<name><surname>Jain</surname>
<given-names>S. K.</given-names></name>
<name><surname>Hassan</surname>
<given-names>A. S. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>72</fpage>
<lpage>75</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000072">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000072">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>15. The solvolysis of 1-chloropropan-2-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000076</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregor</surname>
<given-names>I. K.</given-names></name>
<name><surname>Riggs</surname>
<given-names>N. V.</given-names></name>
<name><surname>Stimson</surname>
<given-names>V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>76</fpage>
<lpage>77</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000076">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000076">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>16. Magnetochemistry of the heaviest elements. Part IX. The system UO&lt;sub&gt;2&lt;/sub&gt;–ThO&lt;sub&gt;2&lt;/sub&gt;–O</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000078</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawson</surname>
<given-names>J. K.</given-names></name>
<name><surname>Roberts</surname>
<given-names>L. E. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>78</fpage>
<lpage>80</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000078">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000078">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>17. Solutions in sulphuric acid. Part XVII. Cryoscopic measurements on some univalent metal sulphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000080</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gillespie</surname>
<given-names>R. J.</given-names></name>
<name><surname>Oubridge</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>80</fpage>
<lpage>89</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000080">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000080">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>18. &lt;i&gt;o&lt;/i&gt;-Mercapto-azo-compounds. Part VIII. Preparation and debenzylation of 2-benzylthio-2′- and -4′-nitroazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burawoy</surname>
<given-names>A.</given-names></name>
<name><surname>Chaudhuri</surname>
<given-names>A.</given-names></name>
<name><surname>Vellins</surname>
<given-names>C. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>90</fpage>
<lpage>95</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>19. &lt;i&gt;o&lt;/i&gt;-Mercapto-azo-compounds. Part IX. Debenzylation of 1-benzylthio-2-phenylazonaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burawoy</surname>
<given-names>A.</given-names></name>
<name><surname>Chaudhuri</surname>
<given-names>A.</given-names></name>
<name><surname>Hyslop</surname>
<given-names>W. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>96</fpage>
<lpage>99</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>20. The chemotherapy of tuberculosis. Part VII. Thiosemicarbazones of substituted phenyl- and pyridyl-benzaldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000100</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cymerman-Craig</surname>
<given-names>J.</given-names></name>
<name><surname>Loder</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>100</fpage>
<lpage>103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000100">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000100">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>21. The decomposition of hydrogen peroxide by ceric salts. Part II. The action of ceric perchlorate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000104</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ardon</surname>
<given-names>Michael</given-names></name>
<name><surname>Stein</surname>
<given-names>Gabriel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>104</fpage>
<lpage>106</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000104">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000104">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>22. The pyrolysis of organomercury compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000106</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carter</surname>
<given-names>H. V.</given-names></name>
<name><surname>Chappell</surname>
<given-names>E. I.</given-names></name>
<name><surname>Warhurst</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>106</fpage>
<lpage>115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000106">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000106">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>23. The addition of thiolacetic acid to ethynylcarbinols and the conversion of the adducts into aldols and αβ-unsaturated aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000116</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bader</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>116</fpage>
<lpage>121</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000116">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000116">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>24. Polynuclear heterocyclic systems. Part IX. &lt;i&gt;n&lt;/i&gt;-π*-Transitions in the spectra of aromatic aza-hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000122</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Walker</surname>
<given-names>I. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>122</fpage>
<lpage>126</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000122">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000122">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>25. Experiments on the synthesis of the pyrethrins. Part X. Intermediates for the synthesis of &lt;i&gt;cis&lt;/i&gt;-pyrethrolone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000126</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Harper</surname>
<given-names>S. H.</given-names></name>
<name><surname>Newman</surname>
<given-names>F. C.</given-names></name>
<name><surname>Thompson</surname>
<given-names>D.</given-names></name>
<name><surname>Smith</surname>
<given-names>R. J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>126</fpage>
<lpage>135</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000126">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000126">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>26. Stereochemical studies of olefinic compounds. Part V. Further observations on the ring fission of 3-chlorotetrahydro-furans and -pyrans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Gold</surname>
<given-names>(Mrs.) J.</given-names></name>
<name><surname>Harper</surname>
<given-names>S. H.</given-names></name>
<name><surname>Stokes</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>136</fpage>
<lpage>142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>27. Sesquiterpenoids. Part VII. The constitution of tenulin, a novel sesquiterpenoid lactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Mayo</surname>
<given-names>P. de</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>142</fpage>
<lpage>149</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>28. Chemistry of nitrosyl complexes. Part II. Exchange of &lt;sup&gt;36&lt;/sup&gt;Cl between nitrosyl chloride and some insoluble metal chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000150</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>J.</given-names></name>
<name><surname>Sowerby</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>150</fpage>
<lpage>153</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000150">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000150">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>29. Deoxypentose nucleic acids. Part VII. A re-examination of the titration curves of sodium deoxyribonucleate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000154</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jordan</surname>
<given-names>D. O.</given-names></name>
<name><surname>Mathieson</surname>
<given-names>A. R.</given-names></name>
<name><surname>Matty</surname>
<given-names>Sheila</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>154</fpage>
<lpage>157</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000154">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000154">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>30. Deoxypentose nucleic acids. Part VIII. The influence of concentration and ionic strength on the electrometric titration of sodium deoxyribonucleate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000158</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jordan</surname>
<given-names>D. O.</given-names></name>
<name><surname>Mathieson</surname>
<given-names>A. R.</given-names></name>
<name><surname>Matty</surname>
<given-names>Sheila</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>158</fpage>
<lpage>163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000158">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000158">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>31. Electrophilic substitution. Part I. Preliminary investigations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bavin</surname>
<given-names>P. M. G.</given-names></name>
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>164</fpage>
<lpage>169</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>32. The kinetics of the alkaline hydrolysis of esters and amides of 1- and 2-naphthoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000170</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fitzgerald</surname>
<given-names>P.</given-names></name>
<name><surname>Packer</surname>
<given-names>J.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>J.</given-names></name>
<name><surname>Wilson</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>170</fpage>
<lpage>173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000170">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000170">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>33. Perfluoroalkyl derivatives of sulphur. Part IV. Perfluoroalkanesulphonic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gramstad</surname>
<given-names>T.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>173</fpage>
<lpage>180</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>34. Mannose-containing polysaccharides. Part IV. The glucomannans of Lily bulbs</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000181</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrews</surname>
<given-names>P.</given-names></name>
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Jones</surname>
<given-names>J. K. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>181</fpage>
<lpage>188</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000181">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000181">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>35. Degradative studies on peptides and proteins. Part II. Synthesis and properties of 3-benzoyl-1-phenyl-2-thiohydantoin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000188</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elmore</surname>
<given-names>D. T.</given-names></name>
<name><surname>Toseland</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>188</fpage>
<lpage>191</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000188">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000188">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>36. Degradative studies on peptides and proteins. Part III. Synthesis of some 2-thiohydantoins as reference compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000192</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elmore</surname>
<given-names>D. T.</given-names></name>
<name><surname>Ogle</surname>
<given-names>J. R.</given-names></name>
<name><surname>Toseland</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>192</fpage>
<lpage>196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000192">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000192">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>37. Specific conductivity measurements directly related to solubilities with special reference to calcium sulphate (anhydrite) solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000196</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Madgin</surname>
<given-names>W. M.</given-names></name>
<name><surname>Swales</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>196</fpage>
<lpage>200</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000196">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000196">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>38. Solutions of alcohols in non-polar solvents. Part III. The viscosities of dilute solutions of primary alcohols in benzene, heptane, and &lt;i&gt;cyclo&lt;/i&gt;hexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000200</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Staveley</surname>
<given-names>L. A. K.</given-names></name>
<name><surname>Taylor</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>200</fpage>
<lpage>209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000200">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000200">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>39. The latent heat of vaporization and the thermochemistry of ethyl nitrate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000210</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>Peter</given-names></name>
<name><surname>Pratt</surname>
<given-names>M. W. T.</given-names></name>
<name><surname>Larkin</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>210</fpage>
<lpage>212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000210">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000210">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>40. Naphthyridines. Part III. Hydroxynaphthyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000212</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hart</surname>
<given-names>E. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>212</fpage>
<lpage>214</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000212">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000212">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000214</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Zervas</surname>
<given-names>L.</given-names></name>
<name><surname>Zioudrou</surname>
<given-names>Miss C.</given-names></name>
<name><surname>Schuler</surname>
<given-names>Bruno O. G.</given-names></name>
<name><surname>Warren</surname>
<given-names>F. L.</given-names></name>
<name><surname>Craw</surname>
<given-names>D. A.</given-names></name>
<name><surname>Rogers</surname>
<given-names>J. L.</given-names></name>
<name><surname>Prasad</surname>
<given-names>K. S. N.</given-names></name>
<name><surname>Raper</surname>
<given-names>R.</given-names></name>
<name><surname>Meek</surname>
<given-names>Eric G.</given-names></name>
<name><surname>Anderson</surname>
<given-names>D. M. W.</given-names></name>
<name><surname>Greenwood</surname>
<given-names>C. T.</given-names></name>
<name><surname>Edward</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>214</fpage>
<lpage>223</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000214">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000214">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Obituary notice: William Godden, 1884–1954</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000224</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cuthbertson</surname>
<given-names>D. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>224</fpage>
<lpage>224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000224">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000224">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>48. The infrared spectra of liquid and solid formic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>225</fpage>
<lpage>229</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>49. The diffusion coefficient of hydrogen in iron</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000230</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stross</surname>
<given-names>T. M.</given-names></name>
<name><surname>Tompkins</surname>
<given-names>F. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>230</fpage>
<lpage>234</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000230">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000230">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>50. Heterocyclic imines and amines. Part VI. Condensation products from di-imino&lt;i&gt;iso&lt;/i&gt;indoline and succinimidine with cyanoacetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000235</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Fitt</surname>
<given-names>John S.</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>235</fpage>
<lpage>243</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000235">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000235">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>51. Compounds containing directly linked pyrrole rings. Part I. A new type of pyrrole pigment</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000244</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Fitt</surname>
<given-names>John S.</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>244</fpage>
<lpage>246</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000244">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000244">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>52. Addition reactions of heterocyclic compounds. Part II. Phenanthridine and methyl acetylenedicarboxylate in methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000246</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Bond</surname>
<given-names>G. J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>246</fpage>
<lpage>250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000246">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000246">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>53. The optical stability of 1 : 2 : 3 : 4-tetrahydro-2-naphthylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000250</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Edwin</surname>
<given-names>E. E.</given-names></name>
<name><surname>Kenyon</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>250</fpage>
<lpage>254</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000250">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000250">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>54. Studies in aromatic nucleophilic substitution. Part IV. Relative nucleophilic powers of common reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000254</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
<name><surname>Hirst</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>254</fpage>
<lpage>260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000254">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000254">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>55. Terpene compounds. Part VIII. The conversion of (±)-benzylidenepiperitone into 3-&lt;i&gt;iso&lt;/i&gt;propylphenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000260</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Adhya</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>260</fpage>
<lpage>263</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000260">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000260">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>56. The reversibility of the adsorption of catalyst poisons. Part IV. Revival of poisoned catalysts by gas-phase desorption</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maxted</surname>
<given-names>E. B.</given-names></name>
<name><surname>Josephs</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>264</fpage>
<lpage>268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>57. Ion-exchange studies of phosphates. Part I. Ion-exchange sorption and pH-titration methods for detection of complex formation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holroyd</surname>
<given-names>A.</given-names></name>
<name><surname>Salmon</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>269</fpage>
<lpage>272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>58. The localization theory of organic reactions. Part III. Radical substitution in pyridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>272</fpage>
<lpage>275</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>59. Binding in some diatomic molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Linnett</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>275</fpage>
<lpage>287</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>60. The effect of α-chloro-substituents on the &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;1 reactivity of the C—Cl linkage</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000287</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bensley</surname>
<given-names>B.</given-names></name>
<name><surname>Kohnstam</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>287</fpage>
<lpage>296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000287">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000287">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>61. 16-Oxo- and 16α-hydroxy-testosterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000297</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adams</surname>
<given-names>(Mrs.) W. J.</given-names></name>
<name><surname>Patel</surname>
<given-names>D. K.</given-names></name>
<name><surname>Petrow</surname>
<given-names>V.</given-names></name>
<name><surname>Stuart-Webb</surname>
<given-names>(Mrs.) I. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>297</fpage>
<lpage>302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000297">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000297">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>62. Deoxypentose nucleic acids. Part IX. The electrophoretic mobility of sodium deoxyribonucleate at various pH values and ionic strengths</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000303</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mathieson</surname>
<given-names>A. R.</given-names></name>
<name><surname>McLaren</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>303</fpage>
<lpage>307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000303">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000303">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>63. The reaction of cyanamide with α-amino-acetals and α-amino-aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000307</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawson</surname>
<given-names>Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>307</fpage>
<lpage>310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000307">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000307">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>64. Enol isomerism in the tropine series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000310</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Friedmann</surname>
<given-names>C. A.</given-names></name>
<name><surname>Gladych</surname>
<given-names>J. M. Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>310</fpage>
<lpage>313</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000310">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000310">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>65. Quinolizines and quinolizidines. Part I. Reduction of 4-oxoquinolizidines by lithium aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000313</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>H. R.</given-names></name>
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>313</fpage>
<lpage>318</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000313">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000313">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>66. The formation and reductive scission of bis-compounds from enols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000319</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>William</given-names></name>
<name><surname>Watkinson</surname>
<given-names>Leonard J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>319</fpage>
<lpage>327</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000319">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000319">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>67. Decahydroisoquinolines and related compounds. Part I. Some 6-oxygenated derivatives and an example of abnormal ultraviolet absorption</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marchant</surname>
<given-names>Alan</given-names></name>
<name><surname>Pinder</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>327</fpage>
<lpage>331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>68. Infrared absorption of halogeno-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Page</surname>
<given-names>J. E.</given-names></name>
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>331</fpage>
<lpage>336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>69. New trypanocides. Part I. Quaternary salts derived from 2 : 7-diaminophenanthridine and the attempted preparation of quaternary salts from 2 : 7-diamino-9-anilinophenanthridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000337</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>337</fpage>
<lpage>343</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>70. The kinetics of the reaction between cobalt(III) and thallium(I) in aqueous perchloric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000343</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ashurst</surname>
<given-names>K. G.</given-names></name>
<name><surname>Higginson</surname>
<given-names>W. C. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>343</fpage>
<lpage>349</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000343">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000343">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>71. Synthesis of polycyclic compounds. Part I. A new synthesis of alkylphenanthrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000350</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Nasipuri</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>350</fpage>
<lpage>354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000350">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000350">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>72. Synthesis of polycyclic compounds. Part II. The ring closure of β-carboxy-&lt;i&gt;γ&lt;/i&gt;-1-naphthylbutyric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Nasipuri</surname>
<given-names>D.</given-names></name>
<name><surname>Adhya</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>355</fpage>
<lpage>358</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>73. Terpene compounds. Part IX. A method of formation of homo&lt;i&gt;apo&lt;/i&gt;camphoric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000358</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adhya</surname>
<given-names>R. N.</given-names></name>
<name><surname>Ghosh</surname>
<given-names>A. C.</given-names></name>
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>358</fpage>
<lpage>361</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000358">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000358">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>74. Anhydro-compounds from nitrogen-containing derivatives of thioglycollic acid. Part II. Glyoxaline and benziminazole compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000361</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duffin</surname>
<given-names>G. F.</given-names></name>
<name><surname>Kendall</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>361</fpage>
<lpage>368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000361">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000361">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>75. The search for chemotherapeutic amidines. Part XII. &lt;i&gt;NN&lt;/i&gt;′-di(amidinophenyl)amidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000368</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crundwell</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>368</fpage>
<lpage>371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000368">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000368">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>76. Peptides. Part V. Condensation of the &lt;i&gt;γ&lt;/i&gt;-carboxyl group of α-glutamyl peptides with the peptide chain</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clayton</surname>
<given-names>D. W.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>371</fpage>
<lpage>380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>77. Reactions of &lt;i&gt;N&lt;/i&gt;-carboxy-α-amino-acid anhydrides catalysed by tertiary bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000381</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>D. G. H.</given-names></name>
<name><surname>Bamford</surname>
<given-names>C. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>381</fpage>
<lpage>387</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000381">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000381">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>78. A novel method of cyanoethylation. Part IV. Substitution effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000388</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bates</surname>
<given-names>R. J.</given-names></name>
<name><surname>Cymerman-Craig</surname>
<given-names>J.</given-names></name>
<name><surname>Moyle</surname>
<given-names>M.</given-names></name>
<name><surname>Young</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>388</fpage>
<lpage>395</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000388">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000388">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>79. 1-Phenylnaphthalenes. Part III. The effect of substituents and their position on the absorption spectra of 1-phenylnaphthalene-2 : 3-dicarboxylic anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000395</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Sawires</surname>
<given-names>Zaki</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>395</fpage>
<lpage>400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000395">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000395">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>80. A spectrophotometric study of hexanitrodiphenylamine. Part I. The molecular and ionic forms in dioxan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kertes</surname>
<given-names>S.</given-names></name>
<name><surname>Goldschmidt</surname>
<given-names>J. M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>401</fpage>
<lpage>404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>81. Mechanism of aromatic side-chain reactions with special reference to the polar effects of substituents. Part XVI. Hyperconjugation of groups of the type CH&lt;sub&gt;2&lt;/sub&gt;X in the benzaldehyde–cyanohydrin equilibria</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>John W.</given-names></name>
<name><surname>Brieux</surname>
<given-names>J. A. L.</given-names></name>
<name><surname>Saunders</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>404</fpage>
<lpage>414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>82. Reactions of substituted 3 : 4-dihydro-4-oxoquinazolines with Grignard reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000415</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kacker</surname>
<given-names>I. K.</given-names></name>
<name><surname>Zaheer</surname>
<given-names>S. Husain</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>415</fpage>
<lpage>418</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000415">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000415">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>83. Galloflavin. Part III. The position of the carboxyl group in &lt;i&gt;iso&lt;/i&gt;galloflavin and a synthesis of trimethylbrevifolin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000418</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimshaw</surname>
<given-names>James</given-names></name>
<name><surname>Haworth</surname>
<given-names>Robert D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>418</fpage>
<lpage>422</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000418">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000418">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>84. The thermochemistry of organic phosphorus compounds. Part II. Ester and anilide formation from halides, and combustion of the anilides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000422</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Neale</surname>
<given-names>E.</given-names></name>
<name><surname>Williams</surname>
<given-names>L. T. D.</given-names></name>
<name><surname>Moores</surname>
<given-names>V. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>422</fpage>
<lpage>427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000422">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000422">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>85. Peroxides as initiators of polymerization of methyl methacrylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000427</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Saha</surname>
<given-names>(the late) N. G.</given-names></name>
<name><surname>Nandi</surname>
<given-names>U. S.</given-names></name>
<name><surname>Palit</surname>
<given-names>Santi R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>427</fpage>
<lpage>436</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000427">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000427">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>86. Complexes of palladium and platinum with certain chelate compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000437</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Livingstone</surname>
<given-names>S. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>437</fpage>
<lpage>440</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000437">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000437">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>87. &lt;i&gt;O&lt;/i&gt;-toluene-&lt;i&gt;p&lt;/i&gt;-sulphonyl derivatives of 1 : 6-anhydro-β-D-altrose and their behaviour towards alkali.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000441</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Newth</surname>
<given-names>F. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>441</fpage>
<lpage>447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000441">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000441">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>88. Steric relations between ionisation of aralkyl chlorides and dissociation of anilinium ions. Part II.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000448</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddeley</surname>
<given-names>G.</given-names></name>
<name><surname>Chadwick</surname>
<given-names>J.</given-names></name>
<name><surname>Taylor</surname>
<given-names>H. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>448</fpage>
<lpage>450</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000448">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000448">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>89. Steric relations between ionisation of aralkyl chlorides and dissociation of anilinium ions. Part III.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000451</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddeley</surname>
<given-names>G.</given-names></name>
<name><surname>Chadwick</surname>
<given-names>J.</given-names></name>
<name><surname>Taylor</surname>
<given-names>H. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>451</fpage>
<lpage>456</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000451">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000451">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>90. Triterpenoids. Part XLVII. The constitution of some compounds obtained by the dehydration of β-amyrin and related alcohols: further observations on the stereochemistry of α-amyrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000456</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allan</surname>
<given-names>G. G.</given-names></name>
<name><surname>Fayez</surname>
<given-names>M. B. E.</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>Robert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>456</fpage>
<lpage>465</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000456">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000456">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000465</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>J. I.</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>Robert</given-names></name>
<name><surname>French</surname>
<given-names>C. M.</given-names></name>
<name><surname>Harrison</surname>
<given-names>D.</given-names></name>
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
<name><surname>Bye</surname>
<given-names>G. C.</given-names></name>
<name><surname>Newth</surname>
<given-names>F. H.</given-names></name>
<name><surname>Ayer</surname>
<given-names>W. A.</given-names></name>
<name><surname>Taylor</surname>
<given-names>W. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>465</fpage>
<lpage>472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000465">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000465">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>96. The conductivity of silver nitrate in non-aqueous and mixed solvents. Part IV</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000473</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>V. S.</given-names></name>
<name><surname>Lawrence</surname>
<given-names>K. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>473</fpage>
<lpage>476</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000473">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000473">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>97. The interaction of &lt;i&gt;aldehydo&lt;/i&gt;-sugars and primary aromatic amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000476</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barclay</surname>
<given-names>J. L.</given-names></name>
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Overend</surname>
<given-names>W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>476</fpage>
<lpage>480</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000476">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000476">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>98. Dambonitol. Part II. Oxidation by periodic acid and sodium metaperiodate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000480</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiang</surname>
<given-names>A. K.</given-names></name>
<name><surname>Loke</surname>
<given-names>K. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>480</fpage>
<lpage>483</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000480">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000480">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>99. The condensation of acridone with tertiary aromatic amines and the ultraviolet absorption spectra of the products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000484</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Robinson</surname>
<given-names>M. J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>484</fpage>
<lpage>489</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000484">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000484">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>100. Oxidation of organic sulphides. Part V. The products of the reaction of organic hydroperoxides with alk-2-enyl sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000489</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnard</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>489</fpage>
<lpage>495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000489">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000489">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>101. The reaction of magnesium halides with αβ-anhydro-sugars</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000496</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Richards</surname>
<given-names>G. N.</given-names></name>
<name><surname>Wiggins</surname>
<given-names>L. F.</given-names></name>
<name><surname>Wise</surname>
<given-names>W. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>496</fpage>
<lpage>500</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000496">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000496">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>102. The mechanism of hydrolysis of acid chlorides. Part VI. Formolysis of &lt;i&gt;para&lt;/i&gt;-substituted benzoyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000501</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crunden</surname>
<given-names>E. W.</given-names></name>
<name><surname>Hudson</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>501</fpage>
<lpage>507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000501">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000501">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>103. Trichloromethyl sulphones and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000508</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Farrar</surname>
<given-names>W. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>508</fpage>
<lpage>513</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000508">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000508">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>104. The oxidation of some 3 : 4-dihydroxyphenethylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000513</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>E. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>513</fpage>
<lpage>517</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000513">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000513">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>105. Partial reduction of steroid hormones and related substances. Part II. A new synthetic route to steroidal 20 : 21-ketols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000517</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norymberski</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>517</fpage>
<lpage>519</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000517">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000517">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>106. Exchange reactions and magnetic susceptibilities of complex salts. Part IV. Correlation with absorption spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000520</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>H. C.</given-names></name>
<name><surname>Odell</surname>
<given-names>A. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>520</fpage>
<lpage>524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000520">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000520">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>107. Equilibria between &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-[(MR&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;PtX&lt;sub&gt;2&lt;/sub&gt;](where M = P, As, and Sb; X = halogen)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000525</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatt</surname>
<given-names>J.</given-names></name>
<name><surname>Wilkins</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>525</fpage>
<lpage>529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000525">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000525">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>108. The synthesis of usnic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000530</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Deflorin</surname>
<given-names>A. M.</given-names></name>
<name><surname>Edwards</surname>
<given-names>O. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>530</fpage>
<lpage>534</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000530">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000530">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>109. Polarography in fused salts. The dipping platinum microelectrode</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000534</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flengas</surname>
<given-names>S. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>534</fpage>
<lpage>538</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000534">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000534">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>110. Ionisation equilibria of metal co-ordination complexes in benzene solution. Part II. The structures of some cuprous complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000538</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burkin</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>538</fpage>
<lpage>541</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000538">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000538">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>111. Cationic polymerisation of oxa&lt;i&gt;cyclo&lt;/i&gt;butanes. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000542</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rose</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>542</fpage>
<lpage>546</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000542">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000542">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>112. Cationic polymerisation of oxa&lt;i&gt;cyclo&lt;/i&gt;butanes. Part II.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000546</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rose</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>546</fpage>
<lpage>555</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000546">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000546">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>113. Interaction of Lewis acids with aromatic hydrocarbons and bases. Part XVI. The association of chloranil with methylbenzenes in &lt;i&gt;cyclo&lt;/i&gt;hexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000555</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foster</surname>
<given-names>R.</given-names></name>
<name><surname>Hammick</surname>
<given-names>D. Ll.</given-names></name>
<name><surname>Parsons</surname>
<given-names>B. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>555</fpage>
<lpage>558</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000555">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000555">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>114. Studies in hydrogen-bond formation. Part IV. The hydrogen-bonding properties of water in non-aqueous solution and of alcohols, aldehydes, carbohydrates, ketones, phenols, and quinones in aqueous and non-aqueous solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000559</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arshid</surname>
<given-names>F. M.</given-names></name>
<name><surname>Giles</surname>
<given-names>C. H.</given-names></name>
<name><surname>Jain</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>559</fpage>
<lpage>569</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000559">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000559">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>115. Organic complex-forming agents for metals. Part I. Preparation of 4-hydroxy- and 4 : 7-dihydroxy-benziminazoles and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000569</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lane</surname>
<given-names>E. S.</given-names></name>
<name><surname>Williams</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>569</fpage>
<lpage>573</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000569">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000569">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>116. Structural and stereochemical investigations of cyclic bases. Part I. 3-(Tertiary amino)-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000573</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gent</surname>
<given-names>B. B.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>573</fpage>
<lpage>578</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000573">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000573">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>117. Alkyl sulphates. Part I. Critical micelle concentrations of the sodium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000579</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>H. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>579</fpage>
<lpage>586</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>118. A quantitative study of the autoxidation products of oleic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000587</article-id><contrib-group><contrib contrib-type="author">
<name><surname>King</surname>
<given-names>George</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>587</fpage>
<lpage>593</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000587">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000587">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>119. Five-covalent terpyridyl complexes of bivalent metals. Part I. The stereochemistry of the zinc, cadmium, and copper compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000594</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Corbridge</surname>
<given-names>D. E. C.</given-names></name>
<name><surname>Cox</surname>
<given-names>E. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>594</fpage>
<lpage>603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000594">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000594">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>120. The constituents of high-boiling petroleum distillates. Part III. Anthracene homologues in a Kuwait oil</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>603</fpage>
<lpage>607</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>121. Solutions in sulphuric acid. Part XVIII. A conductometric investigation of the ionisation of some carboxylic acid anhydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000607</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>R.</given-names></name>
<name><surname>Gillespie</surname>
<given-names>R. J.</given-names></name>
<name><surname>Wasif</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>607</fpage>
<lpage>613</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000607">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000607">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>122. Aromatic azo-compounds. Part VIII. A study of intramolecular hydrogen bonding in 8-hydroxyquinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000614</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Buttery</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>614</fpage>
<lpage>616</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000614">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000614">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>123. Synthetic applications of activated metal catalysts. Part II. The formation of heterocyclic diaryls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000616</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Sasse</surname>
<given-names>W. H. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>616</fpage>
<lpage>620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000616">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000616">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>124. The kinetics of the reduction of some azo-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000620</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Large</surname>
<given-names>N. R.</given-names></name>
<name><surname>Hinshelwood</surname>
<given-names>Sir Cyril</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>620</fpage>
<lpage>627</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000620">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000620">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>125. Modified steroid hormones. Part I. Some 4-bromo-3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000627</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirk</surname>
<given-names>D. N.</given-names></name>
<name><surname>Patel</surname>
<given-names>D. K.</given-names></name>
<name><surname>Petrow</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>627</fpage>
<lpage>629</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000627">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000627">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>126. Chemical examination of &lt;i&gt;Wedelia calendulacea&lt;/i&gt;. Part I. Structure of wedelolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Govindachari</surname>
<given-names>T. R.</given-names></name>
<name><surname>Nagarajan</surname>
<given-names>K.</given-names></name>
<name><surname>Pai</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>629</fpage>
<lpage>632</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>127. An examination of the rutaceae of Hong Kong. Part I. Flavonoid glycosides from &lt;i&gt;Zanthoxylum&lt;/i&gt; species and the occurrence of optically active hesperetin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000632</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arthur</surname>
<given-names>H. R.</given-names></name>
<name><surname>Hui</surname>
<given-names>(Miss) W. H.</given-names></name>
<name><surname>Ma</surname>
<given-names>C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>632</fpage>
<lpage>635</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000632">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000632">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>128. The structure of Bouchardat's dichlorodideoxydulcitol and the synthesis of 1 : 6-diamino-1 : 6-dideoxy-2 : 4-3 : 5-di-&lt;i&gt;O&lt;/i&gt;-methylenedulcitol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000636</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>K.</given-names></name>
<name><surname>Cummings</surname>
<given-names>W. A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>636</fpage>
<lpage>640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000636">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000636">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>129. Metal derivatives of &lt;i&gt;NN&lt;/i&gt;′-diarylamidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000640</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>William</given-names></name>
<name><surname>Wright</surname>
<given-names>Ian</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>640</fpage>
<lpage>648</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>130. &lt;i&gt;o&lt;/i&gt;-Mercapto-azo-compounds. Part X. Reactions of azobenzene-2-sulphenyl bromide and its derivatives with malonic acid, acetone, and acetophenone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000648</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burawoy</surname>
<given-names>A.</given-names></name>
<name><surname>Chaudhuri</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>648</fpage>
<lpage>652</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000648">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000648">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>131. &lt;i&gt;o&lt;/i&gt;-Mercapto-azo-compounds. Part XI. Action of alkali on azobenzene-2-sulphenyl bromide and its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000653</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burawoy</surname>
<given-names>A.</given-names></name>
<name><surname>Chaudhuri</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>653</fpage>
<lpage>658</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>132. A new method of preparation of aryl &lt;i&gt;iso&lt;/i&gt;thiocyanates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000659</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baxter</surname>
<given-names>J. N.</given-names></name>
<name><surname>Cymerman-Craig</surname>
<given-names>J.</given-names></name>
<name><surname>Moyle</surname>
<given-names>M.</given-names></name>
<name><surname>White</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>659</fpage>
<lpage>665</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000659">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000659">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>133. Organic peroxides. Part VI. A stereochemical investigation of the preparation and reactions of 1-phenylethyl hydroperoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000665</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Feld</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>665</fpage>
<lpage>670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000665">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000665">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>134. The dissociation constant of the ion-pair Co(NH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;6&lt;/sub&gt;&lt;sup&gt;3+&lt;/sup&gt;OH&lt;sup&gt;–&lt;/sup&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000671</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Caton</surname>
<given-names>J. A.</given-names></name>
<name><surname>Prue</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>671</fpage>
<lpage>673</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000671">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000671">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>135. The preparation of benziminazoles from α-benzamido-acids and peptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000673</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>R.</given-names></name>
<name><surname>Edward</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>673</fpage>
<lpage>675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000673">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000673">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>136. An ion-sieve reagent for cœsium–alkali-metal separations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000675</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrer</surname>
<given-names>R. M.</given-names></name>
<name><surname>Sammon</surname>
<given-names>D. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>675</fpage>
<lpage>682</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000675">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000675">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>137. Studies on degraded esparto cellulose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000683</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Fordyce</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>683</fpage>
<lpage>687</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000683">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000683">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>138. The &lt;i&gt;Si&lt;/i&gt;–&lt;i&gt;C&lt;/i&gt;&lt;sub&gt;aromatic&lt;/sub&gt; bond in polyphenylsilyl compounds : the acid strengths of the series of acids &lt;i&gt;p&lt;/i&gt;-Me&lt;sub&gt;4–n&lt;/sub&gt;Ph&lt;sub&gt;n–1&lt;/sub&gt;Si·C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;·CO&lt;sub&gt;2&lt;/sub&gt;H</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000688</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatt</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>A. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>688</fpage>
<lpage>691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000688">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000688">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>139. Compounds of potential pharmacological interest. Part 1. Acyl derivatives of 1-amino-3-phenylindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000691</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Philpott</surname>
<given-names>P. G.</given-names></name>
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>691</fpage>
<lpage>698</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000691">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000691">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>140. Compounds of potential pharmacological interest. Part II. Some heterocyclic and carbocyclic systems related to 1-phenylindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000698</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>MacPhee</surname>
<given-names>K. E.</given-names></name>
<name><surname>Philpott</surname>
<given-names>P. G.</given-names></name>
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>698</fpage>
<lpage>705</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000698">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000698">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>141. Compounds of potential pharmacological interest. Part III. 2-Substituted 1-phenylindanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000706</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Dodsworth</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>706</fpage>
<lpage>708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000706">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000706">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>142. Molecular polarisability. The apparent anisotropy of methane and other quasi-spherical molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000708</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>(Mrs.) C. G. Le</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Rao</surname>
<given-names>D. A. A. S. Narayana</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>708</fpage>
<lpage>713</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000708">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000708">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>143. New thiosemicarbazones and 4-oxo-Δ&lt;sup&gt;2&lt;/sup&gt;-thiazolin-2-ylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000713</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Xuong</surname>
<given-names>Ng. D.</given-names></name>
<name><surname>Binon</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>713</fpage>
<lpage>716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000713">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000713">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>144. Stages in oxidations of organic compounds by potassium permanganate. Part VII. Characteristic features of oxidations involving the manganate, MnO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;2–&lt;/sup&gt;, and hypomanganate, MnO&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;3–&lt;/sup&gt;, anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000717</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pode</surname>
<given-names>J. S. F.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>717</fpage>
<lpage>725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000717">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000717">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>145. The thermal decomposition of lead dioxide in air</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000725</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>George</given-names></name>
<name><surname>Copp</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>725</fpage>
<lpage>735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000725">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000725">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>146. The deuteration and exchange of ethylene on evaporated metal catalysts at low temperatures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000735</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kemball</surname>
<given-names>Charles</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>735</fpage>
<lpage>743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000735">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000735">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>147. Thermodynamics of ion association. Part II. Alkaline-earth acetates and formates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000744</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nancollas</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>744</fpage>
<lpage>749</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000744">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000744">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>148. The &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt; mechanism in aromatic compounds. Part XVI.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000750</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolto</surname>
<given-names>Brian A.</given-names></name>
<name><surname>Liveris</surname>
<given-names>Mark</given-names></name>
<name><surname>Miller</surname>
<given-names>Joseph</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>750</fpage>
<lpage>753</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000750">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000750">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>149. Perfluoroalkyl compounds of nitrogen. Part II. The vibrational assignment of trifluoronitrosomethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000754</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mason</surname>
<given-names>(Mrs.) J.</given-names></name>
<name><surname>Banus</surname>
<given-names>(Miss) J.</given-names></name>
<name><surname>Dunderdale</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>754</fpage>
<lpage>759</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000754">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000754">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>150. Perfluoroalkyl compounds of nitrogen. Part III. The vibrational assignment of fluoropicrin, chloropicrin, and bromopicrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000759</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mason</surname>
<given-names>(Mrs.) J.</given-names></name>
<name><surname>Banus</surname>
<given-names>(Miss) J.</given-names></name>
<name><surname>Dunderdale</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>759</fpage>
<lpage>766</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000759">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000759">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>151. The calculation of atom self-polarizabilities and similar quantities in the molecular-orbital theory</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000767</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>767</fpage>
<lpage>769</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000767">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000767">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>152. Alkaloids of &lt;i&gt;Toddalia aculeata&lt;/i&gt;: identity of toddaline with chelerythrine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000769</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Govindachari</surname>
<given-names>T. R.</given-names></name>
<name><surname>Thyagarajan</surname>
<given-names>B. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>769</fpage>
<lpage>771</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000769">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000769">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>153. The constitution of yohimbine and related alkaloids. Part IX. Synthesis of 2-(4 : 5-diethyl-2-pyridyl)-3-ethylindole (alstyrine or coryline) and two related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000771</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lee</surname>
<given-names>T. B.</given-names></name>
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>771</fpage>
<lpage>775</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000771">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000771">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000776</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gibson</surname>
<given-names>M. S.</given-names></name>
<name><surname>McLean</surname>
<given-names>John</given-names></name>
<name><surname>Clark</surname>
<given-names>A. H.</given-names></name>
<name><surname>Coulson</surname>
<given-names>C. A.</given-names></name>
<name><surname>McDonald</surname>
<given-names>B. J.</given-names></name>
<name><surname>Fardon</surname>
<given-names>J. B.</given-names></name>
<name><surname>Farrar</surname>
<given-names>W. V.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Smith</surname>
<given-names>F.</given-names></name>
<name><surname>Mill</surname>
<given-names>G. S.</given-names></name>
<name><surname>Campbell</surname>
<given-names>R.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Jones</surname>
<given-names>Emrys R. H.</given-names></name>
<name><surname>Mann</surname>
<given-names>Frederick G.</given-names></name>
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Carruthers</surname>
<given-names>W.</given-names></name>
<name><surname>Overton</surname>
<given-names>K. H.</given-names></name>
<name><surname>Barclay</surname>
<given-names>J. L.</given-names></name>
<name><surname>Cleaver</surname>
<given-names>A. J.</given-names></name>
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Overend</surname>
<given-names>W. G.</given-names></name>
<name><surname>Rakshit</surname>
<given-names>(Miss) Usha</given-names></name>
<name><surname>Bhattacharyya</surname>
<given-names>K. C.</given-names></name>
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Bradbury</surname>
<given-names>Helena</given-names></name>
<name><surname>Smith</surname>
<given-names>F. J.</given-names></name>
<name><surname>Earle</surname>
<given-names>Patricia J.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>Muriel L.</given-names></name>
<name><surname>Gregory</surname>
<given-names>Rita A.</given-names></name>
<name><surname>Barton</surname>
<given-names>J. W.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>Alles</surname>
<given-names>B. J. P.</given-names></name>
<name><surname>late) </surname>
<given-names>(the</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>776</fpage>
<lpage>797</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000776">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000776">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Obituary notices: Robert Henry Aders Plimmer, 1877–1955; Walter William Reed 1885–1955; Sigmund Otto Rosenheim, 1871–1955; Gwyn Williams, 1904–1955</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000798</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haas</surname>
<given-names>P.</given-names></name>
<name><surname>Jones</surname>
<given-names>R.</given-names></name>
<name><surname>King</surname>
<given-names>Harold</given-names></name>
<name><surname>Bennett</surname>
<given-names>G. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>798</fpage>
<lpage>804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000798">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000798">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>171. The epimeric (±)-1 : 3-diamino&lt;i&gt;cyclo&lt;/i&gt;hexanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000805</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hewgill</surname>
<given-names>F. R.</given-names></name>
<name><surname>Jefferies</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>805</fpage>
<lpage>808</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000805">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000805">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>172. The preparation of some &lt;i&gt;iso&lt;/i&gt;quinoline derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000808</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gibson</surname>
<given-names>M. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>808</fpage>
<lpage>812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000808">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000808">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>173. Some basic esters of 9-xanthenylacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000812</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McConnel</surname>
<given-names>(Miss) R. J.</given-names></name>
<name><surname>Petrow</surname>
<given-names>V.</given-names></name>
<name><surname>Sturgeon</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>812</fpage>
<lpage>814</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000812">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000812">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>174. The synthesis of glucosamine 6-(dihydrogen phosphate)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>J. M.</given-names></name>
<name><surname>Percival</surname>
<given-names>Elizabeth</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>814</fpage>
<lpage>819</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>175. The ammonolysis of methyl 2 : 3-anhydro-D-furanosides. Part II. Methyl 2 : 3-anhydro-5-&lt;i&gt;O&lt;/i&gt;-methyl-α- and -β-D-lyxofuranosides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000819</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>J. M.</given-names></name>
<name><surname>Percival</surname>
<given-names>Elizabeth</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>819</fpage>
<lpage>823</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000819">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000819">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>176. Interaction of boron and hydrogen halides with esters of boronic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000824</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brindley</surname>
<given-names>P. B.</given-names></name>
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>824</fpage>
<lpage>828</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000824">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000824">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>177. The mucilages of &lt;i&gt;Hibiscus esculentus&lt;/i&gt;(okra or bamia fellahi) and &lt;i&gt;Corchorus olitorius&lt;/i&gt;(mulukhia)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000828</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Amin</surname>
<given-names>El S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>828</fpage>
<lpage>832</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000828">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000828">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>178. Chemical action of ionizing radiations in solution. Part XV. Effect of molecular oxygen in the irradiation of aqueous benzene solutions with &lt;i&gt;X&lt;/i&gt;-rays</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000832</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Daniels</surname>
<given-names>M.</given-names></name>
<name><surname>Scholes</surname>
<given-names>G.</given-names></name>
<name><surname>Weiss</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>832</fpage>
<lpage>834</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000832">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000832">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>179. A new synthesis of fluoro-ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000835</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sykes</surname>
<given-names>A.</given-names></name>
<name><surname>Tatlow</surname>
<given-names>J. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>835</fpage>
<lpage>839</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000835">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000835">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>180. The mechanisms of oxidative fission of stereoisomeric 1 : 2-glycos</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000840</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Levesley</surname>
<given-names>(Miss) P.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
<name><surname>Wright</surname>
<given-names>A. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>840</fpage>
<lpage>845</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000840">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000840">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>181. Mechanism of substitution at a saturated carbon atom. Part L. Kinetic effects of phenyl and halogen substituents in alkyl halides on their reactions with halide ions in acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000845</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Hughes</surname>
<given-names>E. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>845</fpage>
<lpage>849</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000845">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000845">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>182. Mechanism of substitution at a saturated carbon atom. Part LI. &lt;i&gt;ortho&lt;/i&gt;-Effects in solvolysis of arylalkyl halides, illustrating steric retardation in a unimolecular substitution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000850</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Charlton</surname>
<given-names>J. C.</given-names></name>
<name><surname>Hughes</surname>
<given-names>E. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>850</fpage>
<lpage>854</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000850">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000850">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>183. Mechanism of substitution at a saturated carbon atom. Part LII. Polar and steric &lt;i&gt;ortho&lt;/i&gt;-effects in bimolecular Finkelstein substitutions of arylalkyl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Charlton</surname>
<given-names>J. C.</given-names></name>
<name><surname>Hughes</surname>
<given-names>E. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>855</fpage>
<lpage>858</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>184. The electronic spectrum of formaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000858</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brand</surname>
<given-names>J. C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>858</fpage>
<lpage>872</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000858">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000858">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>185. The stereochemistry of the tropane alkaloids. Part VIII. The absolute configurations of the nitrogen atoms in some optically active tropanols and derived quaternary salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000873</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kovács</surname>
<given-names>Ödön</given-names></name>
<name><surname>Fodor</surname>
<given-names>Gábor</given-names></name>
<name><surname>Halmos</surname>
<given-names>Miklós</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>873</fpage>
<lpage>876</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000873">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000873">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>186. Complex fluorides. Part IV. The structural chemistry of complex fluorides of the general formula ABF&lt;sub&gt;6&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000876</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>876</fpage>
<lpage>878</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000876">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000876">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>187. The retardation of benzaldehyde autoxidation. Part VII. Further studies of the actions of polycyclic aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000879</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Turner</surname>
<given-names>A. H.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>879</fpage>
<lpage>888</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000879">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000879">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>188. The oxidation of derivatives of &lt;i&gt;o&lt;/i&gt;-phenylenediamine. Part I. Isomeric phenazine pigments obtained by oxidation of 2-aminodiphenylamine hydrochloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000888</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barry</surname>
<given-names>Vincent C.</given-names></name>
<name><surname>Belton</surname>
<given-names>J. G.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Twomey</surname>
<given-names>Dermot</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>888</fpage>
<lpage>893</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000888">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000888">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>189. The oxidation of derivatives of &lt;i&gt;o&lt;/i&gt;-phenylenediamine. Part II. Phenazine pigments obtained from &lt;i&gt;N&lt;/i&gt;-alkyl-, &lt;i&gt;N&lt;/i&gt;-&lt;i&gt;cyclo&lt;/i&gt;alkyl-, &lt;i&gt;N&lt;/i&gt;-alkylphenyl-, and &lt;i&gt;N&lt;/i&gt;-alkoxyphenyl-&lt;i&gt;o&lt;/i&gt;-phenylenediamine hydrochloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000893</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barry</surname>
<given-names>Vincent C.</given-names></name>
<name><surname>Belton</surname>
<given-names>J. G.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Twomey</surname>
<given-names>Dermot</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>893</fpage>
<lpage>895</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000893">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000893">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>190. The oxidation of derivatives of &lt;i&gt;o&lt;/i&gt;-phenylenediamine. Part III. Isomeric phenazine pigments and &lt;i&gt;apo&lt;/i&gt;safranones obtained by oxidation of chlorinated 2-aminodiphenylamine hydrochlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000896</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barry</surname>
<given-names>Vincent C.</given-names></name>
<name><surname>Belton</surname>
<given-names>J. G.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Twomey</surname>
<given-names>Dermot</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>896</fpage>
<lpage>899</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000896">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000896">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>191. The decomposition of inorganic cyanates in water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000900</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kemp</surname>
<given-names>I. A.</given-names></name>
<name><surname>Kohnstam</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>900</fpage>
<lpage>911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000900">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000900">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>192. The synthesis and reactions of branched-chain hydrocarbons. Part X. The rearrangement of α-ethynyl alcohols to unsaturated carbonyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000911</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Hancock</surname>
<given-names>J. W.</given-names></name>
<name><surname>Hickinbottom</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>911</fpage>
<lpage>917</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000911">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000911">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>193. The synthesis of pyrimidin-5-yl sulphides and disulphides. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000917</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>G. R.</given-names></name>
<name><surname>Luthy</surname>
<given-names>Nydia G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>917</fpage>
<lpage>921</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000917">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000917">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>194. Nitramines and nitramides. Part X. The formation of alkyl cations during acid-catalysed decomposition : evidence from (+)-&lt;i&gt;sec&lt;/i&gt;.-butylnitramine and &lt;i&gt;O&lt;/i&gt;-methyl-&lt;i&gt;N&lt;/i&gt;-&lt;i&gt;neo&lt;/i&gt;pentylnitramine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000921</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bruck</surname>
<given-names>Peter</given-names></name>
<name><surname>Denton</surname>
<given-names>I. N.</given-names></name>
<name><surname>Lamberton</surname>
<given-names>Alex. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>921</fpage>
<lpage>925</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000921">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000921">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>195. The crystal structure of the monoclinic modification of 1 : 2-5 : 6-dibenzanthracene. A quantitative &lt;i&gt;X&lt;/i&gt;-ray investigation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
<name><surname>White</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>925</fpage>
<lpage>931</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>196. Long-range effects in alicyclic systems. Part I. The rates of rearrangement of some steroidal dibromides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000932</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Head</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>932</fpage>
<lpage>937</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000932">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000932">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>197. Some new tropine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000938</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foster</surname>
<given-names>R.</given-names></name>
<name><surname>Ing</surname>
<given-names>H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>938</fpage>
<lpage>940</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000938">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000938">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>198. Studies in peroxidase action. Part X. The oxidation of phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000940</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>H.</given-names></name>
<name><surname>Saunders</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>940</fpage>
<lpage>948</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000940">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000940">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>199. The stereochemistry of sesquiethylenediaminetrimethylplatinic iodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000948</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Truter</surname>
<given-names>Mary R.</given-names></name>
<name><surname>Cox</surname>
<given-names>E. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>948</fpage>
<lpage>952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000948">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000948">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>200. Liquid-phase reactions at high pressures. Part X. The rates of some isomerisations and rearrangements</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000953</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>R. T.</given-names></name>
<name><surname>Weale</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>953</fpage>
<lpage>958</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000953">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000953">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>201. Acrylonitrile in organic syntheses. Part II. Conditions for monocyanoethylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000959</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>A. D.</given-names></name>
<name><surname>Stevens</surname>
<given-names>I. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>959</fpage>
<lpage>962</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000959">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000959">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>202. Polyfluoroalkyl compounds of silicon. Part I. Reaction of trichlorosilane with tetrafluoroethylene.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000962</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Marklow</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>962</fpage>
<lpage>970</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000962">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000962">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>203. The disulphones derived by oxidation of the diethyl dithioacetals of D-galactose, D-mannose, and D-glucose with peroxypropionic acid, and their conversion into aldopentoses</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000970</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Taylor</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>970</fpage>
<lpage>980</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000970">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000970">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>204. A new mechanism for the Beckmann rearrangement of ketoximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000980</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
<name><surname>Staskun</surname>
<given-names>Benjamin</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>980</fpage>
<lpage>985</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000980">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000980">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>205. Syntheses in the quinazolone series. Part I. Synthesis of 2 : 3-diaryl-4-quinazolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000985</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Levy</surname>
<given-names>Paul R.</given-names></name>
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>985</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000985">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000985">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>206. Plant gums of the genus &lt;i&gt;Khaya&lt;/i&gt;. The structure of &lt;i&gt;Khaya grandifolia&lt;/i&gt; gum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000989</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Hirst</surname>
<given-names>E. L.</given-names></name>
<name><surname>Matheson</surname>
<given-names>N. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>989</fpage>
<lpage>997</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000989">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000989">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>207. Conductimetric studies in ketonic solvents. Part II. Water in ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560000998</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hughes</surname>
<given-names>S. R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>998</fpage>
<lpage>1001</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560000998">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560000998">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>208. The thermal decomposition of octadeutero&lt;i&gt;cyclo&lt;/i&gt;butane and octafluoro&lt;i&gt;cyclo&lt;/i&gt;butane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001002</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>B. F.</given-names></name>
<name><surname>Pritchard</surname>
<given-names>H. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1002</fpage>
<lpage>1004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001002">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001002">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>209. Kinetic studies in the phosphinyl chloride and phosphorochloridate series. Part V. Evidence for a one-stage mechanism in the hydrolysis of diethyl phosphorochloridate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dostrovsky</surname>
<given-names>I.</given-names></name>
<name><surname>Halmann</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1004</fpage>
<lpage>1007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>210. Infrared spectra of natural products. Part V. The characterisation of carbonyl groups in pentacyclic triterpenoids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001007</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cole</surname>
<given-names>A. R. H.</given-names></name>
<name><surname>Thornton</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1007</fpage>
<lpage>1015</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001007">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001007">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>211. Allenes. Part I. The rearrangement of prop-2-ynyl acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landor</surname>
<given-names>Phyllis D.</given-names></name>
<name><surname>Landor</surname>
<given-names>S. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1015</fpage>
<lpage>1019</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>212. Some 2 : 6-diamino- and 2-amino-6-hydroxy-derivatives of 5-aryl-4 : 5-dihydropyrimidines. A new synthesis of 4-alkyl-5-arylpyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001019</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hitchings</surname>
<given-names>George H.</given-names></name>
<name><surname>Russell</surname>
<given-names>Peter B.</given-names></name>
<name><surname>Whittaker</surname>
<given-names>Norman</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1019</fpage>
<lpage>1028</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001019">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001019">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>213. The constitution and synthesis of fuscin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001028</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Hendrickson</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1028</fpage>
<lpage>1034</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001028">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001028">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>214. Kinetics of the reaction between methyl iodide and trimethylamine in carbon tetrachloride solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001035</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fahim</surname>
<given-names>R. B.</given-names></name>
<name><surname>Moelwyn-Hughes</surname>
<given-names>E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1035</fpage>
<lpage>1041</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001035">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001035">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>215. Complexes of nickel and cobalt with certain chelate compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001042</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Livingstone</surname>
<given-names>S. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1042</fpage>
<lpage>1044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001042">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001042">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>216. Polyazanaphthalenes. Part III. Some derivatives of 1 : 3 : 5- and 1 : 3 : 8-triazanaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oakes</surname>
<given-names>V.</given-names></name>
<name><surname>Pascoe</surname>
<given-names>R.</given-names></name>
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1045</fpage>
<lpage>1054</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>217. Steroids and Walden inversion. Part XXVII. 3α-Cholesterylamine and coprostan-3α-ylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001054</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Richards</surname>
<given-names>H. C.</given-names></name>
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Sly</surname>
<given-names>J. C. P.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1054</fpage>
<lpage>1059</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001054">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001054">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>218. Steroids and Walden inversion. Part XXVIII. The structure of the lactonic acid derived from 6α-hydroxy-2 : 3-&lt;i&gt;sec&lt;/i&gt;ocholestane-2 : 3-dioic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001059</article-id><contrib-group><contrib contrib-type="author">
<name><surname>James</surname>
<given-names>D. R.</given-names></name>
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1059</fpage>
<lpage>1064</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001059">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001059">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>219. Steroids and Walden inversion. Part XXIX. The configurations of the bromination products of 7-oxocholestan-3β-yl acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001064</article-id><contrib-group><contrib contrib-type="author">
<name><surname>James</surname>
<given-names>D. R.</given-names></name>
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1064</fpage>
<lpage>1067</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001064">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001064">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>220. Syntheses of hydrocarbons possibly related to carcinogenic factors in city smoke</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clemo</surname>
<given-names>G. R.</given-names></name>
<name><surname>Ghatge</surname>
<given-names>N. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1068</fpage>
<lpage>1072</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>221. The constitution of an oat-straw xylan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001072</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Wilkie</surname>
<given-names>K. C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1072</fpage>
<lpage>1076</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001072">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001072">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001076</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gibson</surname>
<given-names>M. S.</given-names></name>
<name><surname>Beckett</surname>
<given-names>A. H.</given-names></name>
<name><surname>Jolliffe</surname>
<given-names>G. O.</given-names></name>
<name><surname>Neeman</surname>
<given-names>M.</given-names></name>
<name><surname>Bunton</surname>
<given-names>C. A.</given-names></name>
<name><surname>Spatcher</surname>
<given-names>D. N.</given-names></name>
<name><surname>Atkinson</surname>
<given-names>C. M.</given-names></name>
<name><surname>Brown</surname>
<given-names>C. W.</given-names></name>
<name><surname>Simpson</surname>
<given-names>(the late) J. C. E.</given-names></name>
<name><surname>Lewis</surname>
<given-names>K. G.</given-names></name>
<name><surname>Carasso</surname>
<given-names>J. I.</given-names></name>
<name><surname>Pittman</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1076</fpage>
<lpage>1085</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001076">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001076">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Obituary notices: Philip Rufus Carter, 1921–1955; Salah Eldin Said El Wakkad, 1918–1955; Bernard Jacques Flurscheim, 1874–1955; Harold Augustine Tempany, 1881–1955</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001086</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Moussa</surname>
<given-names>A. A.</given-names></name>
<name><surname>Ingold</surname>
<given-names>C. K.</given-names></name>
<name><surname>Russell</surname>
<given-names>E. John</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1086</fpage>
<lpage>1092</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001086">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001086">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>229. Aliphatic hydroxylamines. Part II. Autoxidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001093</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>David H.</given-names></name>
<name><surname>Rogers</surname>
<given-names>M. A. Thorold</given-names></name>
<name><surname>Trappe</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1093</fpage>
<lpage>1103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001093">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001093">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>230. 2-Mercaptoglyoxalines. Part X. The acylation of 2-mercaptoglyoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001103</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawson</surname>
<given-names>Alexander</given-names></name>
<name><surname>Morley</surname>
<given-names>H. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1103</fpage>
<lpage>1108</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001103">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001103">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>231. The reactions of anthracene and 9-methylanthracene with the free radicals derived from di-&lt;i&gt;tert&lt;/i&gt;.-butyl peroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001108</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beckwith</surname>
<given-names>A. L. J.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1108</fpage>
<lpage>1115</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001108">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001108">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>232. Stabilities of complex compounds of metals. The system di(tri-&lt;i&gt;n&lt;/i&gt;-butylphosphine)dichloropalladium(II)–&lt;i&gt;n&lt;/i&gt;-octylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meddings</surname>
<given-names>B.</given-names></name>
<name><surname>Burkin</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1115</fpage>
<lpage>1123</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>233. Attempted synthesis of 1 : 9-9′ : 1′-dicarbazolylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001124</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Geale</surname>
<given-names>Ann C.</given-names></name>
<name><surname>Linnell</surname>
<given-names>June M. G.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>Muriel L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1124</fpage>
<lpage>1127</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001124">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001124">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>234. The reaction between diphenylpicrylhydrazyl and 2-cyano-2-propyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001127</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevington</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1127</fpage>
<lpage>1132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001127">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001127">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>235. The oxidation of &lt;i&gt;iso&lt;/i&gt;butyraldehyde with the free radical, ·O·N(SO&lt;sub&gt;3&lt;/sub&gt;K)&lt;sub&gt;2&lt;/sub&gt;, from potassium nitrosyldisulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001132</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>G. D.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1132</fpage>
<lpage>1135</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001132">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001132">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>236. Experiments on the preparation of indolocarbazoles. Part VIII. The preparation of 1-methylindolo(2′ : 3′-2 : 3)carbazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001135</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swindells</surname>
<given-names>Margaret L.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>Muriel L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1135</fpage>
<lpage>1138</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001135">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001135">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>237. Structural chemistry of the alkoxides. Part V. Isomeric butoxides and pentyloxides of quinquevalent tantalum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001139</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
<name><surname>Whitley</surname>
<given-names>(Miss) A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1139</fpage>
<lpage>1142</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001139">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001139">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>238. The kinetics of oxidation by nitrous and nitric acid. Part III. Oxidation of oxalic acid by nitrous acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001143</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Vamplew</surname>
<given-names>(Miss) P. A.</given-names></name>
<name><surname>Singer</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1143</fpage>
<lpage>1146</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001143">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001143">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>239. α-Methyleneadipic acid and some related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001146</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Owen</surname>
<given-names>L. N.</given-names></name>
<name><surname>Peto</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1146</fpage>
<lpage>1151</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001146">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001146">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>240. Analogues of cortical hormones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001152</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Edward R.</given-names></name>
<name><surname>Howes</surname>
<given-names>J. G. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1152</fpage>
<lpage>1158</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001152">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001152">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>241. Polynuclear heterocyclic systems. Part I. The synthesis of condensed glyoxalinium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001158</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>B. R.</given-names></name>
<name><surname>Wild</surname>
<given-names>E. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1158</fpage>
<lpage>1163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001158">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001158">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>242. The solubility of aluminium chloride in some hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fairbrother</surname>
<given-names>Fred</given-names></name>
<name><surname>Scott</surname>
<given-names>Norman</given-names></name>
<name><surname>Prophet</surname>
<given-names>Harold</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1164</fpage>
<lpage>1167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>243. Saponins and sapogenins. Part IV. Agapanthagenin (22a-spirostan-2α : 3β : 5α-triol), a new sapogenin from &lt;i&gt;Agapanthus&lt;/i&gt; species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001167</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stephen</surname>
<given-names>(Mrs.) T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1167</fpage>
<lpage>1169</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001167">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001167">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>244. Raman effect of the borohydride ion in liquid ammonia</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001170</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Woodward</surname>
<given-names>L. A.</given-names></name>
<name><surname>Roberts</surname>
<given-names>H. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1170</fpage>
<lpage>1172</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001170">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001170">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>245. Theoretical studies of the macrocyclic pigments. Part I. The structure of bacteriochlorophyll</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001172</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnard</surname>
<given-names>J. R.</given-names></name>
<name><surname>Jackman</surname>
<given-names>L. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1172</fpage>
<lpage>1178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001172">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001172">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>246. Modified steroid hormones. Part II. (i) Monohalogenation of 5α : 6β-dibromocholestan-3-one. (ii) Some 2α-halogenated androgens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001179</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ellis</surname>
<given-names>Bernard</given-names></name>
<name><surname>Petrow</surname>
<given-names>Vladimir</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1179</fpage>
<lpage>1183</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001179">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001179">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>247. Modified steroid hormones. Part III. Some 4-chloro-3-oxo-Δ&lt;sup&gt;4&lt;/sup&gt;-derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001184</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirk</surname>
<given-names>D. N.</given-names></name>
<name><surname>Patel</surname>
<given-names>D. K.</given-names></name>
<name><surname>Petrow</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1184</fpage>
<lpage>1186</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001184">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001184">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>248. The polarography of niobium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001186</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ferrett</surname>
<given-names>D. J.</given-names></name>
<name><surname>Milner</surname>
<given-names>G. W. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1186</fpage>
<lpage>1192</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001186">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001186">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>249. The chemistry of D-ribose and its derivatives. Part VI. &lt;i&gt;iso&lt;/i&gt;Propylidene and benzylidene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001192</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>G. R.</given-names></name>
<name><surname>Spoors</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1192</fpage>
<lpage>1195</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001192">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001192">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>250. The synthesis and stereochemistry of some tervalent arsenic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001195</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>I. G. M.</given-names></name>
<name><surname>Poller</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1195</fpage>
<lpage>1203</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001195">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001195">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>251. The allomerization of chlorophyll</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001203</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnston</surname>
<given-names>L. G.</given-names></name>
<name><surname>Watson</surname>
<given-names>W. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1203</fpage>
<lpage>1212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001203">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001203">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>252. Cellular constituents. The chemistry of xanthine oxidase. Part II. The homogeneity of crystalline metalloflavoprotein fractions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001212</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Avis</surname>
<given-names>P. G.</given-names></name>
<name><surname>Bergel</surname>
<given-names>F.</given-names></name>
<name><surname>Bray</surname>
<given-names>R. C.</given-names></name>
<name><surname>James</surname>
<given-names>D. W. F.</given-names></name>
<name><surname>Shooter</surname>
<given-names>K. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1212</fpage>
<lpage>1219</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001212">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001212">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>253. Cellular constituents. The chemistry of xanthine oxidase. Part III. Estimations of the co-factors and the catalytic activities of enzyme fractions from cow's milk</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001219</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Avis</surname>
<given-names>P. G.</given-names></name>
<name><surname>Bergel</surname>
<given-names>F.</given-names></name>
<name><surname>Bray</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1219</fpage>
<lpage>1226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001219">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001219">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>254. Tracer studies in the formation and reactions of organic per-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001226</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bunton</surname>
<given-names>C. A.</given-names></name>
<name><surname>Lewis</surname>
<given-names>(the late) T. A.</given-names></name>
<name><surname>Llewellyn</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1226</fpage>
<lpage>1230</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001226">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001226">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>255. Studies on phosphorylation. Part XIII. Ketoxime sulphonates as intermediates in pyrophosphate formation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001231</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander R.</given-names></name>
<name><surname>Webb</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1231</fpage>
<lpage>1237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001231">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001231">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>256. Reduced cyclic compounds. Part I. The preparation and cyclodehydration of ω-phenyl unsaturated tertiary alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001238</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Selleck</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1238</fpage>
<lpage>1242</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001238">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001238">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>257. Complex fluorides. Part V. Complexes formed by molybdenum hexafluoride, tungsten hexafluoride, and rhodium tetrafluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001242</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>B.</given-names></name>
<name><surname>Sharp</surname>
<given-names>D. W. A.</given-names></name>
<name><surname>Sharpe</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1242</fpage>
<lpage>1244</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001242">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001242">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Note</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001244</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>D. C. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1244</fpage>
<lpage>1247</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001244">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001244">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chemical effects of steric strains</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001248</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>Herbert C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1248</fpage>
<lpage>1268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001248">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001248">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>259. The ring fission of &lt;i&gt;iso&lt;/i&gt;quinoline–sulphur trioxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Potts</surname>
<given-names>K. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1269</fpage>
<lpage>1271</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>260. Studies in hydrogen-bond formation. Part V. Complex-forming properties of esters, and their relation to the adsorption properties of cellulose acetate and other polymers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arshid</surname>
<given-names>F. M.</given-names></name>
<name><surname>Giles</surname>
<given-names>C. H.</given-names></name>
<name><surname>Jain</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1272</fpage>
<lpage>1277</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>261. A thermodynamic study of some iodine solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001278</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jepson</surname>
<given-names>W. B.</given-names></name>
<name><surname>Rowlinson</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1278</fpage>
<lpage>1285</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001278">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001278">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>262. Kinetics of the depolymerisation of trioxan in aqueous acids, and the acidic properties of aqueous hydrogen fluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001286</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Bascombe</surname>
<given-names>K. N.</given-names></name>
<name><surname>McCoubrey</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1286</fpage>
<lpage>1291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001286">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001286">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>263. The quadrivalent fluororhenates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001291</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peacock</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1291</fpage>
<lpage>1293</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001291">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001291">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>264. Ionization constants of heterocyclic substances. Part II. Hydroxy-derivatives of nitrogenous six-membered ring-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001294</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Phillips</surname>
<given-names>J. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1294</fpage>
<lpage>1304</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001294">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001294">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>265. Esterification by sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001304</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>(the late) Gwyn</given-names></name>
<name><surname>Clark</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1304</fpage>
<lpage>1311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001304">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001304">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>266. The Hg–Hg bond length in the mercurous ion. Part I. The crystal structure of mercurous nitrate dihydrate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001312</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grdenić</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1312</fpage>
<lpage>1316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001312">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001312">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>267. The Hg–Hg bond length in the mercurous ion. Part II. The crystal structure of mercurous fluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001316</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grdenić</surname>
<given-names>D.</given-names></name>
<name><surname>Djordjević</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1316</fpage>
<lpage>1319</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001316">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001316">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>268. The action of acyl cyanides on 2- and 1 : 2-substituted indoles. Part II. Derivatives of 2-&lt;i&gt;o&lt;/i&gt;-aminophenylindole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001319</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kiang</surname>
<given-names>A. K.</given-names></name>
<name><surname>Mann</surname>
<given-names>F. G.</given-names></name>
<name><surname>Prior</surname>
<given-names>A. F.</given-names></name>
<name><surname>Topham</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1319</fpage>
<lpage>1331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001319">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001319">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>269. Cyanine dyes derived from 2-methylindolo(3′ : 2′-3 : 4)quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mann</surname>
<given-names>Frederick G.</given-names></name>
<name><surname>Prior</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1331</fpage>
<lpage>1336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>270. The oxidation of 2-naphthylamine with benzoyl peroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001337</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Orr</surname>
<given-names>S. F. D.</given-names></name>
<name><surname>Sims</surname>
<given-names>Peter</given-names></name>
<name><surname>Manson</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1337</fpage>
<lpage>1344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>271. Synthesis of polycyclic compounds. Part III. The formation of &lt;i&gt;as&lt;/i&gt;-octahydrophenanthrene from the isomeric 2-phenethyl&lt;i&gt;cyclo&lt;/i&gt;hexanols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ray</surname>
<given-names>(Mrs.) Manjuli</given-names></name>
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Bhattacharyya</surname>
<given-names>K. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1344</fpage>
<lpage>1346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>272. Synthesis of polycyclic compounds. Part IV. Substituted 3-alkylphenanthrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Adhya</surname>
<given-names>R. N.</given-names></name>
<name><surname>Bhattacharyya</surname>
<given-names>K. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1346</fpage>
<lpage>1349</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>273. Vibrational frequencies and thermodynamic properties of fluoro-, chloro-, bromo-, and iodo-benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001350</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whiffen</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1350</fpage>
<lpage>1356</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001350">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001350">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>274. Synthesis of di[&lt;i&gt;ar&lt;/i&gt;-&lt;sup&gt;14&lt;/sup&gt;C]benzoyl peroxide from [&lt;sup&gt;14&lt;/sup&gt;C]benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001356</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayrey</surname>
<given-names>G.</given-names></name>
<name><surname>Moore</surname>
<given-names>C. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1356</fpage>
<lpage>1359</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001356">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001356">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>275. The colour of organic compounds. Part VIII. A comparison of isomeric dyes from 3 : 7&lt;i&gt;a&lt;/i&gt;-diazaindan-1-one and -2-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001360</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knott</surname>
<given-names>Edward B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1360</fpage>
<lpage>1364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001360">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001360">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>276. Aryl-2-halogenoalkylamines. Part XVI. The preparation of derivatives of 4-[di-(2-chloroalkyl)amino]azobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ross</surname>
<given-names>W. C. J.</given-names></name>
<name><surname>Warwick</surname>
<given-names>G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1364</fpage>
<lpage>1369</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001364">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>277. Synthesis of oxyayanin-B</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001369</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goel</surname>
<given-names>R. N.</given-names></name>
<name><surname>Jain</surname>
<given-names>A. C.</given-names></name>
<name><surname>Seshadri</surname>
<given-names>T. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1369</fpage>
<lpage>1371</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001369">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001369">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>278. Nucleotides. Part XXXV. &lt;i&gt;cyclo&lt;/i&gt;Pentanone oxime &lt;i&gt;p&lt;/i&gt;-nitro-benzenesulphonate as an intermediate in the synthesis of nucleotide derivatives : an alternative synthesis of adenosine-5′ triphosphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chase</surname>
<given-names>B. H.</given-names></name>
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander R.</given-names></name>
<name><surname>Webb</surname>
<given-names>R. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1371</fpage>
<lpage>1376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>279. Triterpenoids. Part XLVIII. Olean-13(18)-ene : isomerisation of olean-12-ene and related hydrocarbons with mineral acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001377</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brownlie</surname>
<given-names>George</given-names></name>
<name><surname>Fayez</surname>
<given-names>M. B. E.</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>Robert</given-names></name>
<name><surname>Strachan</surname>
<given-names>W. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1377</fpage>
<lpage>1381</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001377">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001377">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>280. The reaction between cinnamic acid and phenols in presence of hydrochloric acid. A new method for the preparation of 3 : 4-dihydro-4-phenylcoumarins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001382</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Simpson</surname>
<given-names>J. D.</given-names></name>
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1382</fpage>
<lpage>1384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001382">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>281. The chemistry of extractives from hardwoods. Part XXVI. Experiments on &lt;i&gt;cyclo&lt;/i&gt;eucalenol, a new triterpene from &lt;i&gt;Eucalyptus microcorys&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>J. S. G.</given-names></name>
<name><surname>King</surname>
<given-names>F. E.</given-names></name>
<name><surname>King</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1384</fpage>
<lpage>1392</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>282. Conductivity studies of some thiosulphates in aqueous methanol and in aqueous ethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>J. R.</given-names></name>
<name><surname>Monk</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1392</fpage>
<lpage>1396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001392">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>283. The influence of electrolytic dissociation upon rates of reactions. Part II. The thiosulphate–propyl bromide reaction in aqueous ethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001396</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>J. R.</given-names></name>
<name><surname>Monk</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1396</fpage>
<lpage>1399</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001396">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001396">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>284. The solvolysis of &lt;i&gt;n&lt;/i&gt;-propyl bromide in aqueous ethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001400</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>J. R.</given-names></name>
<name><surname>Monk</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1400</fpage>
<lpage>1401</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001400">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001400">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>285. Thermochemistry of organophosphorus compounds. Part II. Triethyl phosphate, tripropylphosphine oxide, and tributylphosphine oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chernick</surname>
<given-names>C. L.</given-names></name>
<name><surname>Skinner</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1401</fpage>
<lpage>1405</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>286. The dipole moments of pyridine, quinoline, and &lt;i&gt;iso&lt;/i&gt;quinoline as vapours and as solutes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckingham</surname>
<given-names>A. D.</given-names></name>
<name><surname>Chau</surname>
<given-names>J. Y. H.</given-names></name>
<name><surname>Freeman</surname>
<given-names>H. C.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Rao</surname>
<given-names>D. A. A. S. Narayana</given-names></name>
<name><surname>Tardif</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1405</fpage>
<lpage>1411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>287. Stereochemistry of tropane alkaloids. Part IX. Selective quaternisation of tropan-3α-ol and tropan-3β-ol and of their derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fodor</surname>
<given-names>Gábor</given-names></name>
<name><surname>Koczka</surname>
<given-names>Károly</given-names></name>
<name><surname>Lestyán</surname>
<given-names>János</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1411</fpage>
<lpage>1417</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>288. Mesomorphism and chemical constitution. Part VII. The effect of halogen substitution on the mesomorphism of the &lt;i&gt;trans&lt;/i&gt;-&lt;i&gt;p&lt;/i&gt;-&lt;i&gt;n&lt;/i&gt;-alkoxycinnamic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001417</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>G. W.</given-names></name>
<name><surname>Jones</surname>
<given-names>Brynmor</given-names></name>
<name><surname>Marson</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1417</fpage>
<lpage>1423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001417">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001417">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>289. The conductivity of solutions in which the solvent molecule is “large”. Part I. Solutions of tetraethylammonium picrate in some phthalate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001424</article-id><contrib-group><contrib contrib-type="author">
<name><surname>French</surname>
<given-names>C. M.</given-names></name>
<name><surname>Singer</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1424</fpage>
<lpage>1429</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001424">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001424">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>290. New intermediates and dyes. Part IV. Condensation of thionaphthen-2 : 3-dicarboxylic anhydride with hydrocarbons and phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001429</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peters</surname>
<given-names>Arnold T.</given-names></name>
<name><surname>Walker</surname>
<given-names>Derek</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1429</fpage>
<lpage>1436</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001429">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001429">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>291. Organosilicon compounds. Part XVII. The acidic solvolysis of organosilicon hydrides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001436</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baines</surname>
<given-names>J. E.</given-names></name>
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1436</fpage>
<lpage>1441</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001436">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001436">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>292. Electrophilic substitution. Part II. The nitration of naphthalene and perylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001441</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Mole</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1441</fpage>
<lpage>1443</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001441">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001441">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>293. Glycine peptides. Part II. The heat and entropy of formation of the peptide bond in polyglycine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001444</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meggy</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1444</fpage>
<lpage>1454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001444">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001444">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>294. Liquid metals. Part IV. The wetting of zinc by liquid sodium: the significance of the critical wetting temperature</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Addison</surname>
<given-names>C. C.</given-names></name>
<name><surname>Addison</surname>
<given-names>W. E.</given-names></name>
<name><surname>Kerridge</surname>
<given-names>D. H.</given-names></name>
<name><surname>Lewis</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1454</fpage>
<lpage>1461</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>295. The occurrence of triterpenes in the aquifoliaceae and ericaceae of Hong Kong</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001461</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arthur</surname>
<given-names>H. R.</given-names></name>
<name><surname>Lee</surname>
<given-names>C. M.</given-names></name>
<name><surname>Ma</surname>
<given-names>C. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1461</fpage>
<lpage>1463</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001461">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001461">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>296. Homolytic aromatic substitution. Part XI. The phenylation of toluene, ethylbenzene, and &lt;i&gt;iso&lt;/i&gt;propylbenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Pengilly</surname>
<given-names>B. W.</given-names></name>
<name><surname>Williams</surname>
<given-names>Gareth H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1463</fpage>
<lpage>1475</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>297. Homolytic aromatic substitution. Part XII. Reactions with phenyl iodosobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001475</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
<name><surname>Williams</surname>
<given-names>Gareth H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1475</fpage>
<lpage>1480</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>298. Some chain-substituted methincyanines and styryl dyes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001480</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hamer</surname>
<given-names>Frances M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1480</fpage>
<lpage>1498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001480">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001480">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>299. Reactions of organic azides. Part V. The Schmidt reaction with fluorenones. The structure of the intermediate in the Ketonic Schmidt reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001498</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arcus</surname>
<given-names>C. L.</given-names></name>
<name><surname>Coombs</surname>
<given-names>M. M.</given-names></name>
<name><surname>Evans</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1498</fpage>
<lpage>1506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001498">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001498">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>300. The production of active solids by thermal decomposition. Part VIII. Calcination of calcium hydroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glasson</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1506</fpage>
<lpage>1510</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>301. A new method for the preparation of 9 : 10-disubstituted anthracenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001511</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>K. Jasper</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1511</fpage>
<lpage>1515</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001511">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001511">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>302. Carcinogenic nitrogen compounds. Part XVIII. The synthesis of some polycyclic carbazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001515</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Jacquignon</surname>
<given-names>Pierre</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1515</fpage>
<lpage>1518</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>303. Organic fluorine compounds. Part V. Infrared studies on fluoropyruvic acid and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Kalmus</surname>
<given-names>Abraham</given-names></name>
<name><surname>Pinchas</surname>
<given-names>Shraga</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1519</fpage>
<lpage>1521</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>304. Organic fluorine compounds. Part VI. The enolates of alkyl fluoroacetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001521</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Szinai</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1521</fpage>
<lpage>1524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001521">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001521">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>305. Organic fluorine compounds. Part VII. The Perkin and similar reactions with fluoroacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Schwarcz</surname>
<given-names>José</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1524</fpage>
<lpage>1527</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>306. Addition compounds of gallium trichloride. Part I. A comparison of the binary systems which acyl chlorides form with boron and gallium trichlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001527</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greenwood</surname>
<given-names>N. N.</given-names></name>
<name><surname>Wade</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1527</fpage>
<lpage>1536</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001527">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001527">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>307. Correlation between reactivity of the 1-carbon atom in alcohols, and certain properties of alkoxysilanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Kilburn</surname>
<given-names>K. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1536</fpage>
<lpage>1539</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>308. Stability, solvolysis, and co-ordination reactions of esters of boronic acids and their halogen derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brindley</surname>
<given-names>P. B.</given-names></name>
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1540</fpage>
<lpage>1545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>309. Nucleotides. Part XXXVI. Adenosine-2′ uridine-5′ phosphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001546</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Michelson</surname>
<given-names>A. M.</given-names></name>
<name><surname>Szabo</surname>
<given-names>L.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1546</fpage>
<lpage>1549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001546">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001546">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>310. A study of melanin formation by use of 2-(3 : 4-dihydroxy-[3-&lt;sup&gt;14&lt;/sup&gt;C]phenyl)-, 2-(3 : 4-dihydroxy[4-&lt;sup&gt;14&lt;/sup&gt;C]phenyl)-, and 2-(3 : 4-dihydroxy[5-&lt;sup&gt;14&lt;/sup&gt;C]phenyl)-ethylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001549</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swan</surname>
<given-names>G. A.</given-names></name>
<name><surname>Wright</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1549</fpage>
<lpage>1557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001549">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001549">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>311. The lowest singlet excited levels of naphthalene. Part I. A semi-empirical calculation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001557</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lefebvre</surname>
<given-names>R.</given-names></name>
<name><surname>Moser</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1557</fpage>
<lpage>1563</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001557">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001557">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>312. Nucleophilic displacement reactions in aromatic systems. Part V. Kinetics of the reactions of some chloroazanaphthalenes and related compounds with ethoxide ions and with piperidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001563</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Russell-Hill</surname>
<given-names>D. Q.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1563</fpage>
<lpage>1572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001563">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001563">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>313. Organic reactions in sulphuric acid. Part I. Ester hydrolysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001572</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Leisten</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1572</fpage>
<lpage>1577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>314. An alkaloid of &lt;i&gt;Dioscorea hispida&lt;/i&gt;, dennstedt. Part III. Further investigations of the Hofmann degradation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001577</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pinder</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1577</fpage>
<lpage>1585</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001577">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001577">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>315. &lt;i&gt;peri&lt;/i&gt;-Hydroxy-carbonyl compounds. Part I. The synthesis of &lt;i&gt;peri&lt;/i&gt;-hydroxy-indanones, -tetralones, and -benzo&lt;i&gt;cyclo&lt;/i&gt;heptenones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001585</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hayes</surname>
<given-names>N. F.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1585</fpage>
<lpage>1589</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001585">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001585">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>316. The influence of the reaction medium on the relative apparent electron-donating effects of different alkyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1590</fpage>
<lpage>1596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>317. Adsorption of complex anions from uranyl sulphate solution by anion-exchange resins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001596</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arden</surname>
<given-names>T. V.</given-names></name>
<name><surname>Wood</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1596</fpage>
<lpage>1603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001596">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001596">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>318. Organometallic compounds of the alkali metals. Part VI. Evidence for the formation of free alkyl radicals during certain Wurtz reactions. Homolytic reactions between alkyl-lithium compounds and alkyl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryce-Smith</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1603</fpage>
<lpage>1610</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>319. Fatty acids. Part IV. The preparation of eight 9 : 10 : 12 : 13-tetrahydroxystearic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001611</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bharucha</surname>
<given-names>K. E.</given-names></name>
<name><surname>Gunstone</surname>
<given-names>F. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1611</fpage>
<lpage>1619</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001611">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001611">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>320. Intermediates for the synthesis of optically active methyl-substituted long-chain acids. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001620</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1620</fpage>
<lpage>1622</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001620">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001620">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>321. The selective absorption of optical antipodes by proteins. Part III</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001622</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>William</given-names></name>
<name><surname>Brindley</surname>
<given-names>Richard A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1622</fpage>
<lpage>1627</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001622">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001622">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>322. Reactions of organic azides. Part VI. The interaction of 2-acylbenzoic acids and alkylidenephthalides with hydrazoic and sulphuric acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001627</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arcus</surname>
<given-names>C. L.</given-names></name>
<name><surname>Marks</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1627</fpage>
<lpage>1633</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001627">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001627">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>323. The determination of small concentrations of alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001633</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>V. S.</given-names></name>
<name><surname>Stock</surname>
<given-names>D. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1633</fpage>
<lpage>1635</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001633">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001633">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>324. The mechanism of aromatic sulphonation and desulphonation in aqueous sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001635</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1635</fpage>
<lpage>1641</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001635">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001635">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>325. Some heterocyclic quaternary dichloroiodides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hamer</surname>
<given-names>Frances M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1642</fpage>
<lpage>1643</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>326. Heterocyclyl-rhodanines and -2-thiohydantoins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001644</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knott</surname>
<given-names>Edward B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1644</fpage>
<lpage>1649</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001644">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001644">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>327. Steroids and Walden inversion. Part XXX. The epimeric coprostan-3-ylamines and cholest-4-en-3-ylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001649</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Evans</surname>
<given-names>D. E.</given-names></name>
<name><surname>Richards</surname>
<given-names>H. C.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1649</fpage>
<lpage>1655</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001649">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001649">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>328. Chlorophyll and related substances. Part III. The synthesis of octamethylchlorin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001655</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eisner</surname>
<given-names>Ulli</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
<name><surname>Parkes</surname>
<given-names>E. A.</given-names></name>
<name><surname>Stephen</surname>
<given-names>Edith</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1655</fpage>
<lpage>1661</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001655">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001655">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>329. The β-phenylserine series. Part IV</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001662</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Resnick</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1662</fpage>
<lpage>1665</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001662">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001662">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>330. Diaryl-2 : 2′-disulphonic acids and related compounds. Part I. The diphenyl and the ditolyl series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001665</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Turner</surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1665</fpage>
<lpage>1670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001665">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001665">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>331. The preparation of nitrosoalkanes from alkyl nitrites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001670</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gowenlock</surname>
<given-names>B. G.</given-names></name>
<name><surname>Trotman</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1670</fpage>
<lpage>1675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001670">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001670">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>332. The behaviour of ion-exchange resins with mixed solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001676</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>C. W.</given-names></name>
<name><surname>Owen</surname>
<given-names>B. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1676</fpage>
<lpage>1680</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001676">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001676">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>333. The adsorption of organic acid molecules and their chromatographic separation on ion-exchange resins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001681</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>C. W.</given-names></name>
<name><surname>Owen</surname>
<given-names>B. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1681</fpage>
<lpage>1685</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001681">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001681">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>334. A study of the Stephen reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001686</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Turner</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1686</fpage>
<lpage>1691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001686">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001686">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>335. Mechanism, kinetics, and stereochemistry of octahedral substitutions. Part IV. Bimolecular basic hydrolysis and aquation of some halogenoisothiocyanatobis(ethylenediamine)cobalt(III) ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001691</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ingold</surname>
<given-names>C. K.</given-names></name>
<name><surname>Nyholm</surname>
<given-names>R. S.</given-names></name>
<name><surname>Tobe</surname>
<given-names>M. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1691</fpage>
<lpage>1707</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001691">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001691">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>336. Mechanism, kinetics, and stereochemistry of octahedral substitutions. Part V. Bimolecular basic hydrolysis and aquation of some halogeno- and nitrato-amminobis(ethylenediamine)cobalt(III) ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001707</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nyholm</surname>
<given-names>R. S.</given-names></name>
<name><surname>Tobe</surname>
<given-names>M. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1707</fpage>
<lpage>1718</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001707">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001707">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>337. Aryl-2-halogenoalkylamines. Part XVII. The ultraviolet absorption spectra of some 4-di-(2-chloroethyl)aminoazobenzenes in neutral and acidic ethanol solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001719</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ross</surname>
<given-names>W. C. J.</given-names></name>
<name><surname>Warwick</surname>
<given-names>G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1719</fpage>
<lpage>1724</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001719">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001719">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>338. Aryl-2-halogenoalkylamines. Part XVIII. The rates of reduction of substituted 4-di-(2-chloroethyl)aminoazobenzenes by stannous chloride, hydrazine, and the xanthine oxidase–xanthine system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001724</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ross</surname>
<given-names>W. C. J.</given-names></name>
<name><surname>Warwick</surname>
<given-names>G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1724</fpage>
<lpage>1732</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001724">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001724">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>339. &lt;i&gt;iso&lt;/i&gt;Thebaine: the synthesis of 2 : 3 : 6-trimethoxyaporphine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001732</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>K. W.</given-names></name>
<name><surname>Blues</surname>
<given-names>E. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1732</fpage>
<lpage>1733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001732">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001732">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>340. Synthesis of leprapinic acid and constitution of pinastric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001734</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mittal</surname>
<given-names>O. P.</given-names></name>
<name><surname>Seshadri</surname>
<given-names>T. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1734</fpage>
<lpage>1735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001734">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001734">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>341. The components of wool wax. Part III. 7-Oxocholesterol and the alleged presence of cholestanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Milburn</surname>
<given-names>A. H.</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1736</fpage>
<lpage>1739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>342. The components of wool wax. Part IV. The identification of some steroidal derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001740</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Milburn</surname>
<given-names>A. H.</given-names></name>
<name><surname>Truter</surname>
<given-names>E. V.</given-names></name>
<name><surname>Woodford</surname>
<given-names>F. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1740</fpage>
<lpage>1743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001740">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001740">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>343. Further studies of dihydroxynaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001743</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Lavit</surname>
<given-names>Denise</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1743</fpage>
<lpage>1748</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001743">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001743">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>344. The relative stabilising influences of substituents on free alkyl radicals. Part I. The addition of bromotrichloromethane and butanal to unsaturated acids, esters, and nitriles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001749</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huang</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1749</fpage>
<lpage>1755</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001749">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001749">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>345. The isomerisation of sulphidimines. Part III. The action of chloramine-T on cinnamyl phenyl sulphide, and the hydrolysis and oxidation of &lt;i&gt;N&lt;/i&gt;-substituted toluene-&lt;i&gt;p&lt;/i&gt;-sulphonamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001755</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briscoe</surname>
<given-names>Peter A.</given-names></name>
<name><surname>Challenger</surname>
<given-names>Frederick</given-names></name>
<name><surname>Duckworth</surname>
<given-names>Peter S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1755</fpage>
<lpage>1768</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001755">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001755">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>346. The preparation and stability of dialkyl chloroboronates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001768</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1768</fpage>
<lpage>1774</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001768">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001768">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>347. Photochemical changes of some deoxybenzoins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001774</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenyon</surname>
<given-names>Joseph</given-names></name>
<name><surname>Rassoul</surname>
<given-names>Abdel</given-names></name>
<name><surname>Soliman</surname>
<given-names>Gabra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1774</fpage>
<lpage>1778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001774">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001774">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>348. Methylnicotinic acids. Part I. Condensation of 2-methyl-6-phenylnicotinic acid and its ethyl ester with aldehydes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001778</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tittensor</surname>
<given-names>E.</given-names></name>
<name><surname>Wibberley</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1778</fpage>
<lpage>1781</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001778">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001778">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>349. Oxazolopyridines and oxazoloquinolines. Part I. 2′-Alkyl and 2′-aryl derivatives of oxazolo(4′ : 5′-3 : 4)pyridine and oxazolo(4′ : 5′-3 : 4)quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001781</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fraser</surname>
<given-names>James</given-names></name>
<name><surname>Tittensor</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1781</fpage>
<lpage>1784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001781">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001781">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>350. The structure and reactions of dinitrogen tetroxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001784</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Szabó</surname>
<given-names>Zoltán G.</given-names></name>
<name><surname>Bartha</surname>
<given-names>Lajos G.</given-names></name>
<name><surname>Lakatos</surname>
<given-names>Béla</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1784</fpage>
<lpage>1795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001784">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001784">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>351. The oxidation of hydrocarbons and their derivatives. Part I. The observation of the progress of the reaction by pressure change and by analysis</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001795</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parsons</surname>
<given-names>B. I.</given-names></name>
<name><surname>Danby</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1795</fpage>
<lpage>1798</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001795">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001795">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>352. The oxidation of hydrocarbons and their derivatives. Part II. Structural effects in the ester series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001799</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parsons</surname>
<given-names>B. I.</given-names></name>
<name><surname>Hinshelwood</surname>
<given-names>Sir Cyril</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1799</fpage>
<lpage>1803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001799">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001799">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>353. The oxidation of hydrocarbons and their derivatives. Part III. The rôle of intermediates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parsons</surname>
<given-names>B. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1804</fpage>
<lpage>1809</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>354. Synthesis of polycyclic compounds. Part V. The cyclodehydration of 3-benzyl&lt;i&gt;cyclo&lt;/i&gt;hexanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001809</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Banerjee</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1809</fpage>
<lpage>1812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001809">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001809">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>355. Cyclic sulphites derived from the chloropropanediols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001813</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Millen</surname>
<given-names>D. J.</given-names></name>
<name><surname>Pritchard</surname>
<given-names>J. G.</given-names></name>
<name><surname>Watson</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1813</fpage>
<lpage>1817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001813">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001813">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>356. The structure of sterculic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Faure</surname>
<given-names>P. K.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1818</fpage>
<lpage>1821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>357. The atom polarisation of some co-ordination compounds of metals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001821</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Macqueen</surname>
<given-names>(Mrs.) J.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1821</fpage>
<lpage>1827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001821">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001821">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>358. The chemistry of &lt;i&gt;ψ&lt;/i&gt;-santonin. Part X</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001828</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chopra</surname>
<given-names>N. M.</given-names></name>
<name><surname>Cocker</surname>
<given-names>Wesley</given-names></name>
<name><surname>Edward</surname>
<given-names>J. T.</given-names></name>
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
<name><surname>Stuart</surname>
<given-names>E. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1828</fpage>
<lpage>1833</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001828">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001828">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>359. 1 : 2-3 : 4-8 : 9-10 : 11-Tetrabenzopentacene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001833</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clar</surname>
<given-names>E.</given-names></name>
<name><surname>Kelly</surname>
<given-names>W.</given-names></name>
<name><surname>Niven</surname>
<given-names>W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1833</fpage>
<lpage>1836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001833">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001833">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>360. The reactivity of the &lt;i&gt;O&lt;/i&gt;-acylglycosyl halides. Part IV. The solvolytic reactions of &lt;i&gt;O&lt;/i&gt;-acetyl-α-D-glycosyl 1-halides in the presence of electrophilic catalysts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mattok</surname>
<given-names>G. L.</given-names></name>
<name><surname>Phillips</surname>
<given-names>G. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1836</fpage>
<lpage>1844</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>361. Potential radiosensitizers : some quinones and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001844</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrews</surname>
<given-names>K. J. M.</given-names></name>
<name><surname>Marrian</surname>
<given-names>D. H.</given-names></name>
<name><surname>Maxwell</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1844</fpage>
<lpage>1854</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001844">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001844">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>362. Complex fluorides. Part VI. The properties of silver salts of fluoro-acids and their interaction with aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sharp</surname>
<given-names>D. W. A.</given-names></name>
<name><surname>Sharpe</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1855</fpage>
<lpage>1858</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>363. Complex fluorides. Part VII. The interaction of cuprous salts of fluoro-acids and aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001858</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sharp</surname>
<given-names>D. W. A.</given-names></name>
<name><surname>Sharpe</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1858</fpage>
<lpage>1859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001858">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001858">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>364. The chemistry of the transition elements. Part I. Dimeric carbonyl complexes of platinum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001860</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irving</surname>
<given-names>R. J.</given-names></name>
<name><surname>Magnusson</surname>
<given-names>E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1860</fpage>
<lpage>1863</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001860">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001860">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>365. The morphine–thebaine group of alkaloids. Part VI. The condensation of thebaine with dienophils</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001863</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>K. W.</given-names></name>
<name><surname>Thomas</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1863</fpage>
<lpage>1867</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001863">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001863">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>366. &lt;i&gt;iso&lt;/i&gt;Cyano-complexes of rhodium. Part I. Tetraisocyanorhodium(I) salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001867</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Malatesta</surname>
<given-names>L.</given-names></name>
<name><surname>Vallarino</surname>
<given-names>(Miss) L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1867</fpage>
<lpage>1869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001867">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001867">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>367. Thiazoles derived from chrysean and &lt;i&gt;iso&lt;/i&gt;Chrysean</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001870</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adams</surname>
<given-names>A.</given-names></name>
<name><surname>Slack</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1870</fpage>
<lpage>1877</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001870">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001870">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>368. Purines, pyrimidines, and glyoxalines. Part II. New syntheses of some pyrimidine nucleosides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001877</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ralph</surname>
<given-names>R. K.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1877</fpage>
<lpage>1880</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001877">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001877">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001881</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>R. F.</given-names></name>
<name><surname>Henshall</surname>
<given-names>T.</given-names></name>
<name><surname>Robertson</surname>
<given-names>P. W.</given-names></name>
<name><surname>Landquist</surname>
<given-names>Justus K.</given-names></name>
<name><surname>Green</surname>
<given-names>A. L.</given-names></name>
<name><surname>Buckley</surname>
<given-names>D.</given-names></name>
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Bell</surname>
<given-names>F.</given-names></name>
<name><surname>Buck</surname>
<given-names>K. R.</given-names></name>
<name><surname>Brettle</surname>
<given-names>R.</given-names></name>
<name><surname>Dutton</surname>
<given-names>(Mrs.) A. H.</given-names></name>
<name><surname>Heath</surname>
<given-names>D. F.</given-names></name>
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
<name><surname>Williams</surname>
<given-names>R. J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1881</fpage>
<lpage>1894</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001881">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001881">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The photosynthetic carbon cycle</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calvin</surname>
<given-names>Melvin</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1895</fpage>
<lpage>1915</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Obituary notices: Meredith Gwynne Evans, 1904–1952; James William McBain, 1882–1953; Sydney Glenn Preston Plant, 1896–1955; Humphrey Rivaz Raikes, 1891–1955; Ralph William Ewart Stickings, 1895–1955</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001916</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bawn</surname>
<given-names>C. E. H.</given-names></name>
<name><surname>Taylor</surname>
<given-names>Hugh</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>Muriel</given-names></name>
<name><surname>Hartley</surname>
<given-names>Harold</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1916</fpage>
<lpage>1924</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001916">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001916">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>378. Solutions in sulphuric acid. Part XIX. The formation of tetra(hydrogen sulphato)boric acid and its anion in solutions of boric acid and boric oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>R.</given-names></name>
<name><surname>Gillespie</surname>
<given-names>R. J.</given-names></name>
<name><surname>Oubridge</surname>
<given-names>J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1925</fpage>
<lpage>1938</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>379. Synthesis of 10-methyl-3 : 4-benzopyrene and 8 : 10-dimethyl-3 : 4-benzopyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001938</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1938</fpage>
<lpage>1941</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001938">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001938">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>380. Molecular addition compounds of dinitrogen tetroxide with nitrogen, oxygen, and aromatic hydrocarbon donors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001941</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Addison</surname>
<given-names>C. C.</given-names></name>
<name><surname>Sheldon</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1941</fpage>
<lpage>1949</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>381. Triterpenoids. Part XLIX. The constitution of the ester C&lt;sub&gt;33&lt;/sub&gt;H&lt;sub&gt;46&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt; obtained by oxidation of methyl glycyrrhetate acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001949</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brownlie</surname>
<given-names>George</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1949</fpage>
<lpage>1953</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001949">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001949">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>382. An anomalous reaction of 4 : 6-dichloro-5-nitropyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001953</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rose</surname>
<given-names>F. L.</given-names></name>
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1953</fpage>
<lpage>1956</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001953">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001953">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>383. Griseofulvin. Part X. The orientation of some derivatives of 5-methoxyresorcinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001956</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grove</surname>
<given-names>John Frederick</given-names></name>
<name><surname>Jeffs</surname>
<given-names>P. W.</given-names></name>
<name><surname>Rustidge</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1956</fpage>
<lpage>1963</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001956">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001956">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>384. The morphine–thebaine group of alkaloids. Part VII. A. new method of systematic degradation to nitrogen-free products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001963</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bentley</surname>
<given-names>K. W.</given-names></name>
<name><surname>Ball</surname>
<given-names>J. C.</given-names></name>
<name><surname>Ringe</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1963</fpage>
<lpage>1969</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001963">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001963">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>385. The possible existence of transition-metal complexes of &lt;i&gt;cyclo&lt;/i&gt;butadiene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001969</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Longuet-Higgins</surname>
<given-names>H. C.</given-names></name>
<name><surname>Orgel</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1969</fpage>
<lpage>1972</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001969">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001969">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>386. Aluminium tri-soaps</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001972</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilmour</surname>
<given-names>A.</given-names></name>
<name><surname>Jobling</surname>
<given-names>A.</given-names></name>
<name><surname>Nelson</surname>
<given-names>S. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1972</fpage>
<lpage>1976</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001972">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001972">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>387. Stereochemistry of tervalent arsenic compounds. Part II. Optical resolution of 2-&lt;i&gt;p&lt;/i&gt;-carboxyphenyl-5-methyl-1 : 3-dithia-2-arsaindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001976</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>I. G. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1976</fpage>
<lpage>1979</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001976">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001976">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>388. 7-Nitro-1-naphthylamine. Part I. Its preparation, halogenation, and diazo-coupling; and 1 : 2 : 4 : 7-tetrahalogenonaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001979</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hardy</surname>
<given-names>A.</given-names></name>
<name><surname>Ward</surname>
<given-names>E. R.</given-names></name>
<name><surname>Day</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1979</fpage>
<lpage>1984</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001979">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001979">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>389. The synthesis of some indolylalkylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001984</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Bowman</surname>
<given-names>R. E.</given-names></name>
<name><surname>Evans</surname>
<given-names>D. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1984</fpage>
<lpage>1989</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001984">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001984">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>390. Bridged complexes of palladium(II) containing chelate ligands</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001989</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Livingstone</surname>
<given-names>Stanley E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1989</fpage>
<lpage>1994</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001989">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001989">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>391. Bridged complexes of platinum(II) containing chelate ligands</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560001994</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Livingstone</surname>
<given-names>Stanley E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>1994</fpage>
<lpage>1999</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560001994">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560001994">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>392. Antimalarial studies in the pteridine field</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002000</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Potter</surname>
<given-names>M. D.</given-names></name>
<name><surname>Henshall</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2000</fpage>
<lpage>2005</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002000">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002000">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>393. Quaternary ammonium nitrates. Part II. Reactions of nitratoalkyl ethers, amines, amides, and urethanes with tertiary amines and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002006</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lane</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2006</fpage>
<lpage>2010</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>394. Condensation products of phenols and ketones. Part X. The structure of dianin's compounds, a unique inclusion-forming substance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002010</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>Wilson</given-names></name>
<name><surname>Floyd</surname>
<given-names>A. J.</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>Pope</surname>
<given-names>G.</given-names></name>
<name><surname>Weaving</surname>
<given-names>A. S.</given-names></name>
<name><surname>Wild</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2010</fpage>
<lpage>2017</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002010">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002010">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>395. Condensation products of phenols and ketones. Part XI. A rational synthesis of dianin's compound</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>Wilson</given-names></name>
<name><surname>McOmie</surname>
<given-names>J. F. W.</given-names></name>
<name><surname>Weaving</surname>
<given-names>A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2018</fpage>
<lpage>2020</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>396. The tropylium ion. Part I. Synthesis of tropylium and methyltropylium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002021</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Pettit</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2021</fpage>
<lpage>2025</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002021">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002021">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>397. The tropylium ion. Part II. A further synthesis and some reactions of tropylium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Pettit</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2026</fpage>
<lpage>2029</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>398. Triterpenoids. Part L. The constitution of butyrospermol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002029</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irvine</surname>
<given-names>D. S.</given-names></name>
<name><surname>Lawrie</surname>
<given-names>William</given-names></name>
<name><surname>McNab</surname>
<given-names>A. S.</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2029</fpage>
<lpage>2033</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002029">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002029">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>399. Pyrimidines. Part I. The synthesis of some 5-hydroxypyrimidines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002033</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hull</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2033</fpage>
<lpage>2035</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002033">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002033">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>400. Constituents of the lipids of tubercle bacilli. Part VII. Synthesis of (+)-2(&lt;i&gt;L&lt;/i&gt;) : 4(&lt;i&gt;L&lt;/i&gt;)-dimethyldocosanoic acid, an oxidation product of mycolipenic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fray</surname>
<given-names>G. I.</given-names></name>
<name><surname>Polgar</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2036</fpage>
<lpage>2041</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>401. The reaction of 2-acetamido-2-deoxy-D-glucose with ethanethiol and hydrochloric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002042</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Taha</surname>
<given-names>Mahmoud I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2042</fpage>
<lpage>2048</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002042">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002042">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>402. Carcinogenic nitrogen compounds. Part XIX. The aptitude of some aminoquinolines for cyclisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002048</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Royer</surname>
<given-names>René</given-names></name>
<name><surname>Hubert-Habart</surname>
<given-names>Michel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2048</fpage>
<lpage>2051</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>403. Quinoxaline &lt;i&gt;N&lt;/i&gt;-oxides. Part IV. Derivatives of &lt;i&gt;Py&lt;/i&gt;-hydroxyalkyl-, -aminoalkyl-, and -carboxy-quinoxalines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002052</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landquist</surname>
<given-names>Justus K.</given-names></name>
<name><surname>Silk</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2052</fpage>
<lpage>2058</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002052">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002052">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>404. Quinoxaline &lt;i&gt;N&lt;/i&gt;-oxides. Part V. Further &lt;i&gt;Bz&lt;/i&gt;-substituted derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002058</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Silk</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2058</fpage>
<lpage>2063</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002058">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002058">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>405. The preparation and properties of pyridino(1′ : 2′-2 : 3)-1-oxa-2 : 4-diazol-5-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002063</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2063</fpage>
<lpage>2066</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002063">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002063">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>406. Pteridine studies. Part VIII. The degradation of pteridine. Methylation of the hydroxypteridines and degradation of the products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002066</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Wood</surname>
<given-names>H. C. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2066</fpage>
<lpage>2075</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002066">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002066">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>407. Studies on specific chemical fission of peptide links. Part II. The preparation and hydrolysis of 1-acylpyrrolid-2-ones derived from α-glutamyl peptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002076</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Battersby</surname>
<given-names>Alan R.</given-names></name>
<name><surname>Robinson</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2076</fpage>
<lpage>2084</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002076">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002076">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>408. Colombo root bitter principles. Part I. The functional groups of Columbin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002085</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Elad</surname>
<given-names>Dov</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2085</fpage>
<lpage>2090</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002085">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002085">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>409. Colombo root bitter principles. Part II. The constitution of Columbin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Elad</surname>
<given-names>Dov</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2090</fpage>
<lpage>2095</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>410. The oxidation of chromous perchlorate solutions by molecular oxygen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002095</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ardon</surname>
<given-names>Michael</given-names></name>
<name><surname>Stein</surname>
<given-names>Gabriel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2095</fpage>
<lpage>2097</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002095">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002095">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>411. Solid–liquid equilibria in solutions of non-electrolytes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002097</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rastogi</surname>
<given-names>R. P.</given-names></name>
<name><surname>Varma</surname>
<given-names>K. T. Rama</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2097</fpage>
<lpage>2101</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002097">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002097">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>412. Radiolytic reactions in neutron-irradiated bromobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002101</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Milman</surname>
<given-names>Miriam</given-names></name>
<name><surname>Shaw</surname>
<given-names>P. F. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2101</fpage>
<lpage>2109</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002101">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002101">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>413. The effect of solvent on a simple ion–dipole reaction. Part I. The order and mechanism of the methyl iodide–iodide ion exchange reaction in different solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002110</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Swart</surname>
<given-names>E. R.</given-names></name>
<name><surname>Roux</surname>
<given-names>L. J. le</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2110</fpage>
<lpage>2114</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002110">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002110">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>414. Triterpenes of the friedelane series. Part I. Ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002115</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Courtney</surname>
<given-names>J. L.</given-names></name>
<name><surname>Gascoigne</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2115</fpage>
<lpage>2119</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002115">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002115">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>415. Triterpenes of the friedelane series. Part II. Hydroxy-ketones and alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002119</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Courtney</surname>
<given-names>J. L.</given-names></name>
<name><surname>Gascoigne</surname>
<given-names>R. M.</given-names></name>
<name><surname>Szumer</surname>
<given-names>A. Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2119</fpage>
<lpage>2124</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002119">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002119">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>416. Synthesis of divicine (2 : 4-diamino-5 : 6-dihydroxypyrimidine) and other derivatives of 4 : 5(5 : 6)-dihydroxypyrimidine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002124</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davoll</surname>
<given-names>J.</given-names></name>
<name><surname>Laney</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2124</fpage>
<lpage>2131</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002124">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002124">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>417. Pteridine derivatives. Part II. Methylation of 2 : 4-dihydroxy-6- and –7-phenylpteridine, and related topics</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002131</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dick</surname>
<given-names>G. P. G.</given-names></name>
<name><surname>Wood</surname>
<given-names>H. C. S.</given-names></name>
<name><surname>Logan</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2131</fpage>
<lpage>2136</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002131">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002131">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>418. Arrhenius parameters of some reactions involving multiplicity changes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>Douglas</given-names></name>
<name><surname>Pritchard</surname>
<given-names>H. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2136</fpage>
<lpage>2140</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>419. Studies in the xanthone series. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002140</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>(the late) J. S. H.</given-names></name>
<name><surname>Scheinmann</surname>
<given-names>F.</given-names></name>
<name><surname>Suschitzky</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2140</fpage>
<lpage>2143</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002140">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002140">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>420. Absorption spectra and structure of some solid hydroxyazo-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002143</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hadži</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2143</fpage>
<lpage>2150</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002143">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002143">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>421. The synthesis of 2-deoxy-2-fluorotetritols and 2-deoxy-2-fluoro-(±)-glyceraldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002150</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>N. F.</given-names></name>
<name><surname>Kent</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2150</fpage>
<lpage>2154</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002150">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002150">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>422. The stability of coumarinic acids. Chelation of the hydroxyl group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002155</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawford</surname>
<given-names>Malcolm</given-names></name>
<name><surname>Rasburn</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2155</fpage>
<lpage>2160</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002155">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002155">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>423. Potential antiviral thiourea derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002160</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Xuong</surname>
<given-names>Ng. D.</given-names></name>
<name><surname>Nam</surname>
<given-names>Ng. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2160</fpage>
<lpage>2165</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002160">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002160">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>424. Cyclohexane derivatives. Part II. The mechanism of catalytic hydrogenation of cyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002165</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wicker</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2165</fpage>
<lpage>2173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002165">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002165">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>425. Studies in mycological chemistry. Part V. Synthesis of 2 : 5-dihydroxy-7-methyl-1 : 4-naphthaquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>J. E.</given-names></name>
<name><surname>Roberts</surname>
<given-names>John C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2173</fpage>
<lpage>2176</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>426. Demethoxykanugin: a new crystalline compound from &lt;i&gt;Pongamia glabra&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002176</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mittal</surname>
<given-names>O. P.</given-names></name>
<name><surname>Seshadri</surname>
<given-names>T. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2176</fpage>
<lpage>2178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002176">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002176">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>427. Terpene compounds. Part X. A synthesis of (±)-angustione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002179</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Adhya</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2179</fpage>
<lpage>2181</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002179">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002179">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>428. The effect of sulphur dioxide on the oxidation of copper</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mills</surname>
<given-names>T.</given-names></name>
<name><surname>Evans</surname>
<given-names>U. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2182</fpage>
<lpage>2196</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>429. The constitution of the neutral, tetracyclic triterpenes of dammar resin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002196</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mills</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2196</fpage>
<lpage>2202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002196">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002196">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>430. The structure of isatin and substituted isatins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Sullivan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Sadler</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2202</fpage>
<lpage>2207</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>431. The auxochromic effect of the &lt;i&gt;cyclo&lt;/i&gt;butane ring</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002208</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wren</surname>
<given-names>J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2208</fpage>
<lpage>2212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002208">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002208">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>432. The Friedel–Crafts reaction in the carbazole series. Part V</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002212</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brooke</surname>
<given-names>D. G.</given-names></name>
<name><surname>Plant</surname>
<given-names>(the late) S. G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2212</fpage>
<lpage>2214</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002212">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002212">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>433. Alkylperoxy-radicals. Part II. Kinetics of autoxidations retarded by 2 : 4 : 6-trialkylphenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002215</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bickel</surname>
<given-names>A. F.</given-names></name>
<name><surname>Kooyman</surname>
<given-names>E. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2215</fpage>
<lpage>2221</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002215">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002215">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>434. The mechanism of the Fries rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002222</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cullinane</surname>
<given-names>N. M.</given-names></name>
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>E. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2222</fpage>
<lpage>2231</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002222">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002222">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>435. The preparation of &lt;i&gt;cyclo&lt;/i&gt;pentenones from the products of stobbe condensations with aliphatic ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002231</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elliott</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2231</fpage>
<lpage>2241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002231">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002231">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>436. The structure and mechanism of formation of the polymer obtained from &lt;i&gt;cyclo&lt;/i&gt;propane by mercury photosensitisation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ivin</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2241</fpage>
<lpage>2253</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>437. Congeners of pyridine-4-carboxyhydrazide. Part I. Derivatives of 4-cyanopyridine and 2-cyanothiazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002253</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Libman</surname>
<given-names>D. D.</given-names></name>
<name><surname>Slack</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2253</fpage>
<lpage>2257</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002253">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002253">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>438. Determination of the degree of polymerisation of reducing oligosaccharides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002258</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peat</surname>
<given-names>Stanley</given-names></name>
<name><surname>Whelan</surname>
<given-names>W. J.</given-names></name>
<name><surname>Roberts</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2258</fpage>
<lpage>2260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002258">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002258">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>439. Structural chemistry of the alkoxides. Part VI. Primary alkoxides of quadrivalent cerium and thorium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002260</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Chatterjee</surname>
<given-names>A. K.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2260</fpage>
<lpage>2264</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002260">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002260">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>440. Benzoyloxylation, halogenation, and phenylation of aromatic compounds by silver bromide dibenzoate and silver iodide dibenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryce-Smith</surname>
<given-names>D.</given-names></name>
<name><surname>Clarke</surname>
<given-names>Peter</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2264</fpage>
<lpage>2272</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>441. Chlorophyll and related compounds. Part IV. The position of the extra hydrogens in chlorophyll. The oxidation of pyrophœophorbide-&lt;i&gt;a&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ficken</surname>
<given-names>G. E.</given-names></name>
<name><surname>Johns</surname>
<given-names>R. B.</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2272</fpage>
<lpage>2280</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>442. Chlorophyll and related compounds. Part V. The dihydrohœmatinic acids and their imides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002280</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ficken</surname>
<given-names>G. E.</given-names></name>
<name><surname>Johns</surname>
<given-names>R. B.</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2280</fpage>
<lpage>2283</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002280">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002280">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>443. Halogenation in acid solution. The formation of iodoform from malonic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002283</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2283</fpage>
<lpage>2286</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002283">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002283">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>444. The relation between configuration and conjugation in diphenyl derivatives. Part VI. Some alkyldiphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002286</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Everitt</surname>
<given-names>Pauline M.</given-names></name>
<name><surname>Hall</surname>
<given-names>D. Muriel</given-names></name>
<name><surname>Turner</surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2286</fpage>
<lpage>2290</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002286">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002286">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>445. The use of deactivated charcoals for the isolation of aromatic substances</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002291</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Asatoor</surname>
<given-names>A.</given-names></name>
<name><surname>Dalgliesh</surname>
<given-names>C. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2291</fpage>
<lpage>2299</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002291">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002291">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>446. The micro-flame detector in gas–liquid partition chromatography : correlation of response with heats of combustion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002299</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henderson</surname>
<given-names>J. I.</given-names></name>
<name><surname>Knox</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2299</fpage>
<lpage>2302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002299">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002299">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>447. Absorption spectra of ketones. Part IV. The steric requirements for spectroscopic interaction between a carbonyl group and a βγ-double bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Wariyar</surname>
<given-names>N. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2302</fpage>
<lpage>2311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>448. Pyrimidine reactions. Part I. Pyrimidines from malondiamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002312</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2312</fpage>
<lpage>2314</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002312">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002312">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>449. Caulosapogenin and its identity with hederagenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McShefferty</surname>
<given-names>J.</given-names></name>
<name><surname>Stenlake</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2314</fpage>
<lpage>2316</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>450. The soluble polyglucose of sweet corn (&lt;i&gt;Zea mays&lt;/i&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002317</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peat</surname>
<given-names>Stanley</given-names></name>
<name><surname>Whelan</surname>
<given-names>W. J.</given-names></name>
<name><surname>Turvey</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2317</fpage>
<lpage>2322</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002317">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002317">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>451. Usnic acid. Part XII. Pummerer's ketone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002322</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arkley</surname>
<given-names>Vincent</given-names></name>
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Robertson</surname>
<given-names>Alexander</given-names></name>
<name><surname>Sidisunthorn</surname>
<given-names>Padet</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2322</fpage>
<lpage>2328</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002322">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002322">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>452. The S&lt;sub&gt;N&lt;/sub&gt; mechanism in aromatic compounds. Part XXI</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002329</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heppolette</surname>
<given-names>R. L.</given-names></name>
<name><surname>Miller</surname>
<given-names>Joseph</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2329</fpage>
<lpage>2334</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002329">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002329">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>453. Stereochemical aspects of aromatic substitution. Part I. &lt;i&gt;peri&lt;/i&gt;-Derivatives of naphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002335</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>F.</given-names></name>
<name><surname>Gibson</surname>
<given-names>J. A.</given-names></name>
<name><surname>Wilson</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2335</fpage>
<lpage>2340</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002335">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002335">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>454. Stereochemical aspects of aromatic substitution. Part II. Derivatives of &lt;i&gt;tert&lt;/i&gt;.-butylbenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002340</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>F.</given-names></name>
<name><surname>Wilson</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2340</fpage>
<lpage>2345</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002340">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002340">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>455. Thiadiazoles. Part III. 3-amino-5-arylamino- and 3 : 5-di(aralkylamino)-1 : 2 : 4-thiadiazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002345</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2345</fpage>
<lpage>2352</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002345">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002345">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>456. A new chromatographic procedure and its application to high polymers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002352</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>C. A.</given-names></name>
<name><surname>Williams</surname>
<given-names>R. J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2352</fpage>
<lpage>2362</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002352">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002352">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>457. Stereochemistry of &lt;i&gt;cyclo&lt;/i&gt;hexane derivatives. Part III. Hydroxylation of (+)-&lt;i&gt;trans&lt;/i&gt;-&lt;i&gt;p&lt;/i&gt;-menth-2-ene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002363</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jefferies</surname>
<given-names>P. R.</given-names></name>
<name><surname>Milligan</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2363</fpage>
<lpage>2370</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002363">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002363">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>458. The relative tendencies of simple monoamines to form co-ordination compounds : the stability constants of some amine–platinous complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002371</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatt</surname>
<given-names>J.</given-names></name>
<name><surname>Gamlen</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2371</fpage>
<lpage>2378</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002371">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002371">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>459. A synthesis of 3 : 4-benzopyrene-1 : 5-quinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002379</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2379</fpage>
<lpage>2380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002379">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002379">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>460. Normal alkoxides of quinquevalent niobium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002381</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Chakravarti</surname>
<given-names>B. N.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2381</fpage>
<lpage>2384</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002381">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002381">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>461. The structures of some acylcytosines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander</given-names></name>
<name><surname>Varadarajan</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2384</fpage>
<lpage>2387</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>462. Nucleotides. Part XXXVII. The structure of uridylic acids &lt;i&gt;a&lt;/i&gt; and &lt;i&gt;b&lt;/i&gt;, and a synthesis of spongouridine (3-β-D-arabofuranosyluracil)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002388</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander</given-names></name>
<name><surname>Varadarajan</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2388</fpage>
<lpage>2393</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002388">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002388">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>463. The effect of peptising agents on the crystal growth of insoluble metal salts. Part I. Precipitation in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002393</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Packter</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2393</fpage>
<lpage>2404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002393">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002393">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>464. The preparation of some substituted pyridine 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2404</fpage>
<lpage>2408</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>465. Oxygen heterocycles. Part V. Phenoxathiin derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002408</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lescot</surname>
<given-names>Elie</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>Ng. Ph.</given-names></name>
<name><surname>Xuong</surname>
<given-names>N. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2408</fpage>
<lpage>2411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002408">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002408">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>466. 1 : 8-Dihydroxynaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002412</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Lavit</surname>
<given-names>Denise</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2412</fpage>
<lpage>2415</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002412">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002412">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>467. Gibberellic acid. Part III. Synthesis of fluorenone-4 : 5-dicarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002415</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mulholland</surname>
<given-names>T. P. C.</given-names></name>
<name><surname>Ward</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2415</fpage>
<lpage>2417</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002415">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002415">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>468. Triterpenoids. Part LI. The isolation and characterisation of glabric acid, a new triterpenoid acid from liquorice root</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002417</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaton</surname>
<given-names>J. M.</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2417</fpage>
<lpage>2419</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002417">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002417">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>469. Triterpenoids. Part LII. The constitution and stereochemistry of friedelin and cerin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002419</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brownlie</surname>
<given-names>George</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
<name><surname>Stevenson</surname>
<given-names>Robert</given-names></name>
<name><surname>Strachan</surname>
<given-names>W. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2419</fpage>
<lpage>2427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002419">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002419">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>470. The conductivity of solutions in which the solvent molecule is “large”. Part II. Solutions of tetrapentylammonium picrate in some phthalate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>French</surname>
<given-names>C. M.</given-names></name>
<name><surname>Singer</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2428</fpage>
<lpage>2430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>471. An approach to the total synthesis of triterpenes. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Thomas</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2431</fpage>
<lpage>2443</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>472. Phthalaldehydes and related compounds. Part VII. Further applications of the &lt;i&gt;N&lt;/i&gt;-bromosuccinimide preparative method</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blair</surname>
<given-names>John</given-names></name>
<name><surname>Logan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Newbold</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2443</fpage>
<lpage>2446</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>473. Oxidation by manganese dioxide of some unsaturated alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002446</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bharucha</surname>
<given-names>K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2446</fpage>
<lpage>2447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002446">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002446">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>474. The ionization of ethyleneimine and polyethyleneimine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002448</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shepherd</surname>
<given-names>E. J.</given-names></name>
<name><surname>Kitchener</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2448</fpage>
<lpage>2452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002448">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002448">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>475. Hydroxylations with potassium manganate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002452</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rigby</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2452</fpage>
<lpage>2454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002452">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002452">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>476. Interdependence of molecular conformation and conjugation in aromatic ethers. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002455</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddeley</surname>
<given-names>G.</given-names></name>
<name><surname>Smith</surname>
<given-names>N. H. P.</given-names></name>
<name><surname>Vickars</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2455</fpage>
<lpage>2462</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002455">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002455">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>477. The hydrolysis of phosphonate esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>R. F.</given-names></name>
<name><surname>Keay</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2463</fpage>
<lpage>2469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>478. Isolation and properties of pure actinomycins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Roussos</surname>
<given-names>G. G.</given-names></name>
<name><surname>Vining</surname>
<given-names>L. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2469</fpage>
<lpage>2474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>479. The extraction of indium from hydrobromic acid into mixed organic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002475</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irving</surname>
<given-names>H.</given-names></name>
<name><surname>Rossotti</surname>
<given-names>F. J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2475</fpage>
<lpage>2477</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>480. The synthesis of 1 : 2-dihydro-1-oxo-5′-phenylfurano-(2′ : 3′-3 : 4)&lt;i&gt;iso&lt;/i&gt;quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002477</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Swallow</surname>
<given-names>D. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2477</fpage>
<lpage>2482</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002477">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002477">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>481. The rearrangement of ketones containing tertiary alkyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002483</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>S.</given-names></name>
<name><surname>Porter</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2483</fpage>
<lpage>2485</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002483">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002483">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>482. Thermodynamic ionization constants of barbituric acid and some of its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002485</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Biggs</surname>
<given-names>A. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2485</fpage>
<lpage>2488</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002485">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002485">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>483. Steroids and Walden inversion. Part XXXII. The 3 : 5-&lt;i&gt;cyclo&lt;/i&gt;steroid rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002488</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2488</fpage>
<lpage>2491</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002488">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002488">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>484. Steroids and Walden inversion. Part XXXIII. The configurations of the coprostanyl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002492</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Bridgwater</surname>
<given-names>R. J.</given-names></name>
<name><surname>Jones</surname>
<given-names>D. N.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2492</fpage>
<lpage>2499</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002492">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002492">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>485. Electrometric titration of the sodium salts of deoxyribonucleic acids. Part III. The effect of sodium chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>R. A.</given-names></name>
<name><surname>Peacocke</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2499</fpage>
<lpage>2512</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>486. Quantitative aspects of the base-catalysed halogenation of aliphatic ketones. Part I. Iodination of methyl ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002512</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cullis</surname>
<given-names>C. F.</given-names></name>
<name><surname>Hashmi</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2512</fpage>
<lpage>2521</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002512">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002512">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>487. Infrared spectra and the polymorphism of glycerides. Part II. 1 : 3-Diglycerides and saturated triglycerides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002522</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2522</fpage>
<lpage>2528</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002522">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002522">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>488. The kinetics and mechanisms of some colour reactions of aromatic nitro-compounds at low temperatures. Part II. 2 : 4 : 6-Trinitroanisole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002528</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainscough</surname>
<given-names>J. B.</given-names></name>
<name><surname>Caldin</surname>
<given-names>E. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2528</fpage>
<lpage>2539</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002528">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002528">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>489. The kinetics and mechanisms of some colour reactions of aromatic nitro-compounds at low temperatures. Part III. S-Trinitrobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002540</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainscough</surname>
<given-names>J. B.</given-names></name>
<name><surname>Caldin</surname>
<given-names>E. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2540</fpage>
<lpage>2546</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002540">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002540">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>490. The kinetics and mechanisms of some colour reactions of aromatic nitro-compounds at low temperatures. Part IV. 2 : 4 : 6-Trinitrotoluene : a second reaction with ethoxide ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002546</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ainscough</surname>
<given-names>J. B.</given-names></name>
<name><surname>Caldin</surname>
<given-names>E. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2546</fpage>
<lpage>2549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002546">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002546">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002550</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Varma</surname>
<given-names>J. P.</given-names></name>
<name><surname>Nath</surname>
<given-names>Bhola</given-names></name>
<name><surname>Aggarwal</surname>
<given-names>J. S.</given-names></name>
<name><surname>Landquist</surname>
<given-names>Justus K.</given-names></name>
<name><surname>Bowman</surname>
<given-names>R. E.</given-names></name>
<name><surname>Evans</surname>
<given-names>D. D.</given-names></name>
<name><surname>Bharucha</surname>
<given-names>K. R.</given-names></name>
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Mole</surname>
<given-names>T.</given-names></name>
<name><surname>Stephenson</surname>
<given-names>(Miss) E. F. M.</given-names></name>
<name><surname>Brown</surname>
<given-names>M. G.</given-names></name>
<name><surname>Rigby</surname>
<given-names>W.</given-names></name>
<name><surname>Abrahams</surname>
<given-names>S. C.</given-names></name>
<name><surname>Speakman</surname>
<given-names>J. C.</given-names></name>
<name><surname>Davies</surname>
<given-names>T.</given-names></name>
<name><surname>Staveley</surname>
<given-names>L. A. K.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Thomas</surname>
<given-names>D. B.</given-names></name>
<name><surname>Drummond</surname>
<given-names>J. L.</given-names></name>
<name><surname>Welch</surname>
<given-names>G. A.</given-names></name>
<name><surname>Green</surname>
<given-names>A. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2550</fpage>
<lpage>2567</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Obituary notices: David Runciman Boyd, 1872–1955; Wallace Frank Short, 1898–1955; </article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002568</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adam</surname>
<given-names>N. K.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2568</fpage>
<lpage>2572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002568">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002568">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>505. The nucleotide sequence in deoxypentosenucleic acids. Part I. The action of mercaptoacetic acid on calf-thymus deoxyribonucleic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002573</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Letham</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2573</fpage>
<lpage>2578</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002573">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002573">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>506. The nucleotide sequence in deoxypentosenucleic acids. Part II. The alkaline degradation of calf-thymus &lt;i&gt;aldehydo&lt;/i&gt;apurinic acid di(carboxymethyl) dithioacetal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002579</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Letham</surname>
<given-names>D. S.</given-names></name>
<name><surname>Stacey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2579</fpage>
<lpage>2583</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>507. The nucleotide sequence in deoxypentosenucleic acids. Part III. The nature of the end groups produced by the alkaline hydrolysis of calf-thymus &lt;i&gt;aldehydo&lt;/i&gt;apurinic acid di(carboxymethyl) dithioacetal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002584</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>A. S.</given-names></name>
<name><surname>Letham</surname>
<given-names>D. S.</given-names></name>
<name><surname>Stacey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2584</fpage>
<lpage>2586</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002584">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002584">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>508. 2-Methylbut-2-ene nitrosochloride and its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002587</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thorne</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2587</fpage>
<lpage>2589</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002587">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002587">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>509. The reaction of dialkyl sulphites with sodium iodide in acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002589</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Hancock</surname>
<given-names>E. B.</given-names></name>
<name><surname>Overend</surname>
<given-names>W. G.</given-names></name>
<name><surname>Robb</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2589</fpage>
<lpage>2592</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002589">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002589">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>510. Carcinogenic nitrogen compounds. Part XX. Benzacridines, benzocarbazoles, and benzophenarsazines with hydrogenated rings</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002593</article-id><contrib-group><contrib contrib-type="author">Ng.<name><surname>Jacquignon</surname>
<given-names>Pierre</given-names></name>
<name><surname>Lavit</surname>
<given-names>Denise</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2593</fpage>
<lpage>2596</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>511. Diazepines. Part I. Condensation of acetylacetone with 1 : 2-diamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002597</article-id><contrib-group><contrib contrib-type="author">
<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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2597</fpage>
<lpage>2600</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002597">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002597">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>512. Constitution of tamarind-seed polysaccharides, and the structure of the xylan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002600</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Savur</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2600</fpage>
<lpage>2603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002600">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002600">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>513. The synthesis of thionaphthen derivatives. Part I. The cyclisation of arylthioacetaldehyde diethyl acetals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banfield</surname>
<given-names>J. E.</given-names></name>
<name><surname>Davies</surname>
<given-names>W.</given-names></name>
<name><surname>Ennis</surname>
<given-names>B. C.</given-names></name>
<name><surname>Middleton</surname>
<given-names>S.</given-names></name>
<name><surname>Porter</surname>
<given-names>Q. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2603</fpage>
<lpage>2608</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>514. Polymerisation of thiophen derivatives. Part V. The self-condensation of 4 : 5- and 6 : 7-benzothionaphthen 1 : 1-dioxides. A new route to 1-1′-and 4-2′-naphthylphenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002609</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>W.</given-names></name>
<name><surname>Porter</surname>
<given-names>Q. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2609</fpage>
<lpage>2614</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002609">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002609">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>515. The interaction of aluminium bromide with olefins and with benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002614</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fairbrother</surname>
<given-names>Fred</given-names></name>
<name><surname>Field</surname>
<given-names>Kenneth</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2614</fpage>
<lpage>2619</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002614">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002614">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>516. Tropolones. Part IX. 2 : 3-Dihydro-2 : 3-methylene-1 : 4-naphthaquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002620</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buchanan</surname>
<given-names>G. L.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>J. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2620</fpage>
<lpage>2628</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002620">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002620">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>517. Studies in pyrolysis. Part VI. Competitive routes in the pyrolysis of acyl cyanides and their dimeric forms</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002628</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bennett</surname>
<given-names>R. N.</given-names></name>
<name><surname>Jones</surname>
<given-names>E.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2628</fpage>
<lpage>2631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002628">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002628">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>518. Hybridization in the ground state of the hydrogen molecule-ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>B. F.</given-names></name>
<name><surname>Pritchard</surname>
<given-names>H. O.</given-names></name>
<name><surname>Sumner</surname>
<given-names>F. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2631</fpage>
<lpage>2635</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>519. Studies of the strength of poison-to-catalyst bonds. Part I. Heats of adsorption of ethyl sulphide and thiophen on platinum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002635</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maxted</surname>
<given-names>E. B.</given-names></name>
<name><surname>Josephs</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2635</fpage>
<lpage>2639</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002635">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002635">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>520. The pyrolysis of chloroalkenes. Part III. The molecular mode of decomposition of the 1 : 2-dichloroethylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002640</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodall</surname>
<given-names>(Miss) A. M.</given-names></name>
<name><surname>Howlett</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2640</fpage>
<lpage>2646</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>521. Electrometric titration of the sodium salts of deoxyribonucleic acids. Part IV. Denaturation by heat in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002646</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>R. A.</given-names></name>
<name><surname>Peacocke</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2646</fpage>
<lpage>2651</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002646">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002646">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>522. Benzo[&lt;i&gt;a&lt;/i&gt;]perylene and some of its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clar</surname>
<given-names>E.</given-names></name>
<name><surname>Kelly</surname>
<given-names>W.</given-names></name>
<name><surname>Stewart</surname>
<given-names>D. G.</given-names></name>
<name><surname>Wright</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2652</fpage>
<lpage>2656</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>523. Ribose and its derivatives. Part VII. The condensation of methyl D-ribopyranoside with acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002656</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barker</surname>
<given-names>G. R.</given-names></name>
<name><surname>Spoors</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2656</fpage>
<lpage>2658</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002656">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002656">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>524. The intensity of ultraviolet light absorption by monocrystals. Part I. Measurement of thickness of thin crystals by interferometry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002658</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bree</surname>
<given-names>A.</given-names></name>
<name><surname>Lyons</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2658</fpage>
<lpage>2662</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002658">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002658">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>525. The intensity of ultraviolet light absorption by monocrystals. Part II. Absorption and reflection by anthracene of plane-polarised light</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002662</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bree</surname>
<given-names>A.</given-names></name>
<name><surname>Lyons</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2662</fpage>
<lpage>2670</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002662">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002662">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>526. The structure of cyperone. Part V. The steric course of reduction of the cyperones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002670</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howe</surname>
<given-names>R.</given-names></name>
<name><surname>McQuillin</surname>
<given-names>F. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2670</fpage>
<lpage>2675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002670">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002670">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>527. Addition reactions of heterocyclic compounds. Part III. 2 : 3-Benzacridine and some dienophils</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002676</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Jefford</surname>
<given-names>C. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2676</fpage>
<lpage>2679</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002676">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002676">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>528. Aryldihydroresorcinols. Part I. Dihydro-5-α-naphthyl- and 5-(4-diphenylyl)dihydro-resorcinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002679</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayling</surname>
<given-names>E. E.</given-names></name>
<name><surname>Hodges</surname>
<given-names>(the late) J.</given-names></name>
<name><surname>Meredith</surname>
<given-names>R. F. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2679</fpage>
<lpage>2683</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002679">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002679">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>529. Perfluoroalkyl derivatives of sulphur. Part V. αα-Difluoro-α-(trifluorothio)acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002684</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>Nyman</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2684</fpage>
<lpage>2689</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002684">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002684">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>530. &lt;i&gt;Aconitum&lt;/i&gt; and &lt;i&gt;delphinium&lt;/i&gt; alkaloids. Part I. The environment of the nitrogen atom in delpheline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002689</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Trevett</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2689</fpage>
<lpage>2695</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002689">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002689">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>531. The heats of combustion of quinol and &lt;i&gt;p&lt;/i&gt;-benzoquinone and the thermodynamic quantities of the oxidation–reduction reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002695</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pilcher</surname>
<given-names>G.</given-names></name>
<name><surname>Sutton</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2695</fpage>
<lpage>2700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002695">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002695">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>532. Butadienes and related compounds. Part III. Further study of the factors bearing on the formation of 1 : 1 : 4 : 4-tetra-arylbuta-1 : 3-dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002701</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tadros</surname>
<given-names>Wadie</given-names></name>
<name><surname>Sakla</surname>
<given-names>Alfy Badie</given-names></name>
<name><surname>Akhookh</surname>
<given-names>Youssef</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2701</fpage>
<lpage>2704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002701">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002701">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>533. Oxidation of dialkyl sulphides and trisubstituted phosphines by dinitrogen tetroxide; molecular addition compounds with dialkyl sulphoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002705</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Addison</surname>
<given-names>C. C.</given-names></name>
<name><surname>Sheldon</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2705</fpage>
<lpage>2708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002705">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002705">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>534. Double melting of molecular addition compounds of dinitrogen tetroxide with organic donors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002709</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Addison</surname>
<given-names>C. C.</given-names></name>
<name><surname>Sheldon</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2709</fpage>
<lpage>2712</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002709">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002709">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>535. An infrared spectroscopic investigation of absorption due to the N–H stretching modes of vibration in co-ordination compounds of ammonia and amines. Hydrogen bonding (N–H…Cl) in a series of amine complexes of platinous chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chatt</surname>
<given-names>J.</given-names></name>
<name><surname>Duncanson</surname>
<given-names>L. A.</given-names></name>
<name><surname>Venanzi</surname>
<given-names>L. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2712</fpage>
<lpage>2725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>536. Infrared spectra and structure of some quinone monoximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002725</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hadži</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2725</fpage>
<lpage>2731</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002725">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002725">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>537. The reduction of β-alkylnaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002731</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. C.</given-names></name>
<name><surname>Staveley</surname>
<given-names>C. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2731</fpage>
<lpage>2733</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002731">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002731">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>538. The lowest singlet excited levels of naphthalene. Part II. Restricted calculations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002734</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lefebvre</surname>
<given-names>R.</given-names></name>
<name><surname>Moser</surname>
<given-names>C. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2734</fpage>
<lpage>2739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002734">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002734">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>539. Interrelationship between viscosity and boiling point of homologous liquids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002740</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palit</surname>
<given-names>Santi R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2740</fpage>
<lpage>2743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002740">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002740">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>540. The kinetics of hydrogen isotope exchange reactions. Part V. Partial rate factors for the hydrogen isotope exchange reaction between toluene and sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002743</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2743</fpage>
<lpage>2746</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002743">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002743">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>541. Reactions of disodium pentacyanoamminoferrate with aromatic amines. Part I. The preparation and properties of compounds containing the pentacyano-&lt;i&gt;p&lt;/i&gt;-hydroxyanilinoferrate ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002747</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Herington</surname>
<given-names>E. F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2747</fpage>
<lpage>2752</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002747">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002747">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>542. Infrared spectra and polar effects. Part III. Internal spectral relationships</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002753</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellamy</surname>
<given-names>L. J.</given-names></name>
<name><surname>Williams</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2753</fpage>
<lpage>2757</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002753">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002753">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>543. The activation of carbon–carbon double bonds by cationic catalysts. Part II. The effect of &lt;i&gt;para&lt;/i&gt;-substituents and of solvents on the dimerization of diarylethylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002757</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Jones</surname>
<given-names>N.</given-names></name>
<name><surname>Jones</surname>
<given-names>Peter M. S.</given-names></name>
<name><surname>Thomas</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2757</fpage>
<lpage>2770</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002757">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002757">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>544. Electrochemical studies on polonium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002770</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bagnall</surname>
<given-names>K. W.</given-names></name>
<name><surname>Freeman</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2770</fpage>
<lpage>2774</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002770">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002770">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>545. Molecular polarisability. The molar Kerr constants of benzyl alcohol and aniline at infinite dilution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002775</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroney</surname>
<given-names>M.</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2775</fpage>
<lpage>2778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002775">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002775">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>546. Compounds of silicon. Part I. Silicon derivatives of β-amino-α&lt;i&gt;γ&lt;/i&gt;-diphenylcrotononitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2779</fpage>
<lpage>2784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>547. Aliphatic hydroxylamines. Part III. Reaction with diazotised aromatic amines. A novel synthesis of acylbenzenes from the corresponding amine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002784</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogers</surname>
<given-names>M. A. Thorold</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2784</fpage>
<lpage>2789</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002784">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002784">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>548. The rates of solvolysis of certain arylmethyl chlorides, and a simple molecular-orbital treatment of this and similar reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002789</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Sampson</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2789</fpage>
<lpage>2797</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002789">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002789">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>549. The ionisation functions of cyanoacetic acid in relation to the structure of water and the hydration of ions and molecules</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002798</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feates</surname>
<given-names>F. S.</given-names></name>
<name><surname>Ives</surname>
<given-names>D. J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2798</fpage>
<lpage>2812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002798">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002798">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>550. Phosphorylation through glyoxalines [iminazoles] and its significance in enzymic transphosphorylation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002812</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddiley</surname>
<given-names>J.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Letters</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2812</fpage>
<lpage>2817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002812">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002812">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>551. Chemical studies in the biosynthesis of purine nucleotides. Part I. The preparation of &lt;i&gt;N&lt;/i&gt;-glycylglycosylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002818</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddiley</surname>
<given-names>J.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Handschumacher</surname>
<given-names>R. E.</given-names></name>
<name><surname>Prescott</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2818</fpage>
<lpage>2823</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002818">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002818">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>552. The oxidation of monohydric phenols by alkaline ferricyanide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002823</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haynes</surname>
<given-names>C. G.</given-names></name>
<name><surname>Turner</surname>
<given-names>A. H.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2823</fpage>
<lpage>2831</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002823">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002823">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>553. α-1 : 4-Glucosans. Part IV. A re-examination of the molecular structure of floridean starch</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002831</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fleming</surname>
<given-names>I. D.</given-names></name>
<name><surname>Hirst</surname>
<given-names>E. L.</given-names></name>
<name><surname>Manners</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2831</fpage>
<lpage>2836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002831">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002831">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>554. Reaction-kinetic investigations of the incomplete dissociation of salts. Part IV. The neutralization of nitroethane by solutions of metallic hydroxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002836</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Panckhurst</surname>
<given-names>M. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2836</fpage>
<lpage>2840</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002836">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002836">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>555. An X-ray examination of the crystal structure of &lt;i&gt;p&lt;/i&gt;-iodonitrosobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002841</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Webster</surname>
<given-names>Monica S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2841</fpage>
<lpage>2845</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002841">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002841">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>556. The determination of acid strengths of organic hydroperoxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002845</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnard</surname>
<given-names>D.</given-names></name>
<name><surname>Hargrave</surname>
<given-names>K. R.</given-names></name>
<name><surname>Higgins</surname>
<given-names>G. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2845</fpage>
<lpage>2849</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002845">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002845">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>557. The spectra of some solid cobaltic nitroammines and certain other cobaltic complexes in the 2—15 &lt;i&gt;µ&lt;/i&gt; region</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002849</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beattie</surname>
<given-names>I. R.</given-names></name>
<name><surname>Tyrrell</surname>
<given-names>H. J. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2849</fpage>
<lpage>2853</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002849">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002849">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>558. Potential antituberculosis agents of the indole series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002853</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Doyle</surname>
<given-names>F. P.</given-names></name>
<name><surname>Ferrier</surname>
<given-names>(Mrs.) W.</given-names></name>
<name><surname>Holland</surname>
<given-names>D. O.</given-names></name>
<name><surname>Mehta</surname>
<given-names>M. D.</given-names></name>
<name><surname>Nayler</surname>
<given-names>J. H. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2853</fpage>
<lpage>2857</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002853">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002853">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>559. The anodic oxidation of copper–tin (speculum) alloys at very low current density</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002857</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wakkad</surname>
<given-names>(the late) S. E. S. El</given-names></name>
<name><surname>Salem</surname>
<given-names>T. M.</given-names></name>
<name><surname>ElDin</surname>
<given-names>A. M. Shams</given-names></name>
<name><surname>Hanafi</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2857</fpage>
<lpage>2861</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002857">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002857">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>560. Mechanism, kinetics, and stereochemistry of octahedral substitutions. Part VI. Bimolecular basic hydrolysis and aquation of the chloronitrobis(ethylenediamine)cobalt(III) ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002862</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ašperger</surname>
<given-names>S.</given-names></name>
<name><surname>Ingold</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2862</fpage>
<lpage>2879</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002862">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002862">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>561. Metal carbonyl compounds. Part II. Some carbonyl compounds of ruthenium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002879</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Irving</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2879</fpage>
<lpage>2881</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002879">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002879">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>562. The hydrothermal chemistry of the silicates. Part VII. Synthetic potassium aluminosilicates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002882</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrer</surname>
<given-names>R. M.</given-names></name>
<name><surname>Baynham</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2882</fpage>
<lpage>2891</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002882">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002882">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>563. Synthetic chabazites: correlation between isomorphous replacements, stability, and sorption capacity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002892</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrer</surname>
<given-names>R. M.</given-names></name>
<name><surname>Baynham</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2892</fpage>
<lpage>2903</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002892">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002892">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>564. The chemistry of triterpenes and related compounds. Part XXVIII. β-Boswellic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002904</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beton</surname>
<given-names>J. L.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Jones</surname>
<given-names>E. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2904</fpage>
<lpage>2909</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002904">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002904">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>565. Decarboxylative acylations with α-phenylglycine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002910</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawson</surname>
<given-names>Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2910</fpage>
<lpage>2913</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002910">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002910">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>566. Raman spectra and constitution of solid hydrates. Hydroxonium perchlorate, nitrate, hydrogen sulphate, and sulphate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002913</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Millen</surname>
<given-names>D. J.</given-names></name>
<name><surname>Vaal</surname>
<given-names>E. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2913</fpage>
<lpage>2915</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002913">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002913">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>567. The degradation of carbohydrates by alkali. Part XII. 6-&lt;i&gt;O&lt;/i&gt;-methyl- and 3 : 6- and 4 : 6-di-&lt;i&gt;O&lt;/i&gt;-methyl-D-glucose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002916</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenner</surname>
<given-names>J.</given-names></name>
<name><surname>Richards</surname>
<given-names>G. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2916</fpage>
<lpage>2921</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002916">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002916">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>568. The degradation of carbohydrates by alkali. Part XIII. 2 : 3-Di-&lt;i&gt;O&lt;/i&gt;-methylglucose and its conversion into 5-hydroxymethylfurfuraldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002921</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenner</surname>
<given-names>J.</given-names></name>
<name><surname>Richards</surname>
<given-names>G. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2921</fpage>
<lpage>2925</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002921">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002921">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>569. Griseoviridin. Part III. Degradation to 10-aminodecanoic acid, and other reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002925</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Bowman</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2925</fpage>
<lpage>2928</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002925">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002925">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>570. Compounds of potential pharmacological interest. Part IV. Aryl and alkyl derivatives of 1-aminoindane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002928</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Philpott</surname>
<given-names>P. G.</given-names></name>
<name><surname>MacPhee</surname>
<given-names>K. E.</given-names></name>
<name><surname>Hunt</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2928</fpage>
<lpage>2940</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002928">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002928">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>571. Glycine peptides. Part III. The absorption of orange II by polyglycine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002940</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meggy</surname>
<given-names>A. B.</given-names></name>
<name><surname>Sims</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2940</fpage>
<lpage>2948</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002940">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002940">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>572. Kinetics of the reaction between benzoyl peroxide and phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002948</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Batten</surname>
<given-names>J. J.</given-names></name>
<name><surname>Mulcahy</surname>
<given-names>M. F. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2948</fpage>
<lpage>2959</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002948">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002948">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>573. Structural effects in the reaction between benzoyl peroxide and phenols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002959</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Batten</surname>
<given-names>J. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2959</fpage>
<lpage>2966</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002959">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002959">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>574. The anodic behaviour of lead in halide solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002966</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briggs</surname>
<given-names>G. W. D.</given-names></name>
<name><surname>Wynne-Jones</surname>
<given-names>W. F. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2966</fpage>
<lpage>2971</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002966">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002966">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>575. A synthesis of (±)-pulegone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002971</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Black</surname>
<given-names>C.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>G. L.</given-names></name>
<name><surname>Jarvie</surname>
<given-names>(Miss) A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2971</fpage>
<lpage>2973</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002971">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002971">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>576. The isomeric eudesmols and their association with carissone in &lt;i&gt;Eucalyptus macarthuri&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002973</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McQuillin</surname>
<given-names>F. J.</given-names></name>
<name><surname>Parrack</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2973</fpage>
<lpage>2978</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002973">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002973">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>577. The diffusion in water of some association colloids and solubilised materials</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002978</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brudney</surname>
<given-names>N.</given-names></name>
<name><surname>Saunders</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2978</fpage>
<lpage>2982</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002978">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002978">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>578. Organic complex-forming agents for metals. Part II. Preparation of 5-hydroxy- and 5 : 8-dihydroxy-quinoxalines and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002983</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lane</surname>
<given-names>E. S.</given-names></name>
<name><surname>Williams</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2983</fpage>
<lpage>2986</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002983">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002983">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>579. The preparation, &lt;i&gt;via&lt;/i&gt; thiuronium salts, of optically active thiols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002987</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arcus</surname>
<given-names>C. L.</given-names></name>
<name><surname>Hallgarten</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2987</fpage>
<lpage>2991</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002987">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002987">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>580. Trinuclear dyes related to oxonols. Part II. Formation and absorption spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002991</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jeffreys</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2991</fpage>
<lpage>2995</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002991">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002991">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>581. Chemical constitution and the dissociation constants of monocarboxylic acids. Part XV. Steric effects in substituted nitrobenzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560002995</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dippy</surname>
<given-names>J. F. J.</given-names></name>
<name><surname>Hughes</surname>
<given-names>S. R. C.</given-names></name>
<name><surname>Laxton</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>2995</fpage>
<lpage>3000</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560002995">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560002995">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>582. &lt;i&gt;cyclo&lt;/i&gt;Hexane-1 : 3-diones. Part I. Hydrolysis of ethyl 2 : 4-dioxo-6-styryl&lt;i&gt;cyclo&lt;/i&gt;hexanecarboxylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>G. R.</given-names></name>
<name><surname>Davey</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3001</fpage>
<lpage>3006</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>583. Preparation, stability, and complex formation of aryloxyboron compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003006</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Colclough</surname>
<given-names>T.</given-names></name>
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3006</fpage>
<lpage>3010</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>584. A thermochemical evaluation of bond strengths in some carbon compounds. Part IV. Bond-strength differences based on the reaction: RI + HI → RH + I&lt;sub&gt;2&lt;/sub&gt;, where R =&lt;i&gt;p&lt;/i&gt;-methoxyphenyl and &lt;i&gt;cyclo&lt;/i&gt;hexyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003011</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brennan</surname>
<given-names>D.</given-names></name>
<name><surname>Ubbelohde</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3011</fpage>
<lpage>3016</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003011">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003011">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>585. The polarographic reduction of xanthone and methoxyxanthones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003016</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whitman</surname>
<given-names>W. E.</given-names></name>
<name><surname>Wiles</surname>
<given-names>L. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3016</fpage>
<lpage>3019</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003016">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003016">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>586. Hydrogen overpotential at electrodeposited copper in hydrochloric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003020</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wakkad</surname>
<given-names>(the late) S. E. El</given-names></name>
<name><surname>Ammar</surname>
<given-names>I. A.</given-names></name>
<name><surname>Sabry</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3020</fpage>
<lpage>3024</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003020">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003020">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>587. The enzymic synthesis and degradation of starch. Part XXII. Evidence of multiple branching in waxy-maize starch. A correction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003025</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Peat</surname>
<given-names>Stanley</given-names></name>
<name><surname>Whelan</surname>
<given-names>W. J.</given-names></name>
<name><surname>Thomas</surname>
<given-names>Gwen J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3025</fpage>
<lpage>3030</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003025">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003025">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>588. Ferrocene derivatives. Part III. &lt;i&gt;Cyclo&lt;/i&gt;pentadienyliron carbonyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003030</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hallam</surname>
<given-names>B. F.</given-names></name>
<name><surname>Pauson</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3030</fpage>
<lpage>3037</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003030">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003030">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>589. The reaction of triphenyl phosphite with the halogens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003038</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>G. S.</given-names></name>
<name><surname>Payne</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3038</fpage>
<lpage>3043</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003038">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003038">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>590. The organic chemistry of phosphorus. Part III. The nature of the compounds of triaryl phosphites and the halogens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003043</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
<name><surname>Tonge</surname>
<given-names>B. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3043</fpage>
<lpage>3056</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003043">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003043">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>591. Oxidation of organic sulphides. Part VII. The mechanism of autoxidation of but-2-enyl methyl sulphide, methyl 1-methylbut-2-enyl sulphide, and &lt;i&gt;n&lt;/i&gt;-butyl methyl sulphide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003056</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bateman</surname>
<given-names>L.</given-names></name>
<name><surname>Cunneen</surname>
<given-names>J. I.</given-names></name>
<name><surname>Ford</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3056</fpage>
<lpage>3064</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003056">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003056">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>592. Benzyloxymalondialdehyde. An intermediate in the oxidation of 2-&lt;i&gt;O&lt;/i&gt;-benzyl-D-arabinose with sodium periodate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003065</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Schwarz</surname>
<given-names>J. C. P.</given-names></name>
<name><surname>MacDougall</surname>
<given-names>Myra</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3065</fpage>
<lpage>3069</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003065">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003065">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>593. Hydrogen transfer. Part IX. The selective dehydrogenation of unsaturated alcohols by high-potential quinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003070</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Braude</surname>
<given-names>E. A.</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3070</fpage>
<lpage>3074</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003070">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003070">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>594. A new synthesis of 6 : 8-thioctic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Braude</surname>
<given-names>E. A.</given-names></name>
<name><surname>Linstead</surname>
<given-names>R. P.</given-names></name>
<name><surname>Wooldridge</surname>
<given-names>K. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3074</fpage>
<lpage>3078</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>595. &lt;i&gt;N&lt;/i&gt;-oxides of some hydroxy- and amino-quinolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003079</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ames</surname>
<given-names>D. E.</given-names></name>
<name><surname>Franklin</surname>
<given-names>C. S.</given-names></name>
<name><surname>Grey</surname>
<given-names>T. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3079</fpage>
<lpage>3083</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003079">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003079">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>596. The crystal structure of dimethylketen dimer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003083</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Friedlander</surname>
<given-names>P. H.</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3083</fpage>
<lpage>3087</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>597. Monomethiodides of some 3-substituted 4 : 7-phenanthrolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003087</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sykes</surname>
<given-names>W. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3087</fpage>
<lpage>3092</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003087">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003087">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>598. The pyrolysis of chloroalkenes. Part IV. The radical-chain decomposition of the 1 : 2-dichloroethylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003092</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodall</surname>
<given-names>(Miss) A. M.</given-names></name>
<name><surname>Howlett</surname>
<given-names>K. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3092</fpage>
<lpage>3099</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003092">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003092">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>599. 4-Hydroxyisophthalic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hunt</surname>
<given-names>S. E.</given-names></name>
<name><surname>Jones</surname>
<given-names>J. Idris</given-names></name>
<name><surname>Lindsey</surname>
<given-names>A. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3099</fpage>
<lpage>3107</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>600. The infrared spectra of some metal ammines and deuteroammines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003108</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Powell</surname>
<given-names>D. B.</given-names></name>
<name><surname>Sheppard</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3108</fpage>
<lpage>3113</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003108">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003108">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>601. Some reactions of scandium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003113</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Vickery</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3113</fpage>
<lpage>3120</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003113">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003113">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>602. &lt;i&gt;Aconitum&lt;/i&gt; and &lt;i&gt;delphinium&lt;/i&gt; alkaloids. Part II. Interrelation of the functional groups of delpheline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003121</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Trevett</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3121</fpage>
<lpage>3129</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003121">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003121">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>603. Tetrazolium compounds. Part V. Polarography of triphenyl-tetrazolium bromide and some of its substituted derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003130</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>H.</given-names></name>
<name><surname>Kane</surname>
<given-names>P. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3130</fpage>
<lpage>3139</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003130">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003130">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>604. Trichloromethylthio-derivatives of biological interest</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003139</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sosnovsky</surname>
<given-names>George</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3139</fpage>
<lpage>3141</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003139">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003139">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>605. The aloins. Part I. The structure of barbaloin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003141</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hay</surname>
<given-names>J. Evelyn</given-names></name>
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3141</fpage>
<lpage>3147</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003141">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003141">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>606. Polypeptides. Part II. The preparation of some protected peptides of cysteine and glycine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003148</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hooper</surname>
<given-names>K. C.</given-names></name>
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
<name><surname>Schofield</surname>
<given-names>J. A.</given-names></name>
<name><surname>Heaton</surname>
<given-names>G. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3148</fpage>
<lpage>3156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003148">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003148">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>607. Polypeptides. Part III. The oxidation of some peptides of cysteine and glycine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003157</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heaton</surname>
<given-names>G. S.</given-names></name>
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
<name><surname>Schofield</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3157</fpage>
<lpage>3168</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003157">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003157">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>608. E.m.f. measurements in acetone–water mixtures: the cell H&lt;sub&gt;2&lt;/sub&gt;(Pt)|Cl|AgCl–Ag</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003168</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Feakins</surname>
<given-names>D.</given-names></name>
<name><surname>French</surname>
<given-names>C. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3168</fpage>
<lpage>3172</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003168">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003168">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>609. The chemistry of the triterpenes and related compounds. Part XXIX. The chemistry of butyrospermol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003172</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawson</surname>
<given-names>M. C.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Jones</surname>
<given-names>E. R. H.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Phillips</surname>
<given-names>P. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3172</fpage>
<lpage>3178</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003172">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003172">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>610. The condensation products of malononitrile and certain cyclic keto-amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003179</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ittyerah</surname>
<given-names>P. I.</given-names></name>
<name><surname>Mann</surname>
<given-names>Frederick G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3179</fpage>
<lpage>3183</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003179">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003179">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>611. Ion-exchange studies of solutions of borates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003183</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Everest</surname>
<given-names>D. A.</given-names></name>
<name><surname>Popiel</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3183</fpage>
<lpage>3189</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003183">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003183">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>612. Anhydro-compounds from nitrogen-containing derivatives of thioglycollic (mercaptoacetic) acid. Part III. Arylazo-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003189</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duffin</surname>
<given-names>G. F.</given-names></name>
<name><surname>Kendall</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3189</fpage>
<lpage>3199</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003189">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003189">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>613. Organic fluorine compounds. Part IV. Some reactions of difluoromalonyl chloride, and the action of iodine on disilver difluoromalonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003199</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fear</surname>
<given-names>E. J. P.</given-names></name>
<name><surname>Thrower</surname>
<given-names>J.</given-names></name>
<name><surname>Veitch</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3199</fpage>
<lpage>3204</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003199">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003199">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>614. The chemistry of fluorene. Part V. The preparation of 9 : 9-dialkylfluorenes and the dehydrohalogenation of 9-halogenoalkylfluorenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003204</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Greenhow</surname>
<given-names>E. J.</given-names></name>
<name><surname>McNeil</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3204</fpage>
<lpage>3209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003204">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003204">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>615. Some chlorinated derivatives of phloroglucinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003209</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lloyd</surname>
<given-names>G.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3209</fpage>
<lpage>3212</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003209">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003209">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>616. 3-Aroylcoumarones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3213</fpage>
<lpage>3224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003224</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballantine</surname>
<given-names>J. A.</given-names></name>
<name><surname>Whalley</surname>
<given-names>W. B.</given-names></name>
<name><surname>Mester</surname>
<given-names>L.</given-names></name>
<name><surname>Major</surname>
<given-names>Á.</given-names></name>
<name><surname>Móczár</surname>
<given-names>E.</given-names></name>
<name><surname>Addison</surname>
<given-names>C. C.</given-names></name>
<name><surname>Furmidge</surname>
<given-names>C. G. L.</given-names></name>
<name><surname>Mathur</surname>
<given-names>K. B. L.</given-names></name>
<name><surname>Thakur</surname>
<given-names>R. S.</given-names></name>
<name><surname>Saunders</surname>
<given-names>D. G.</given-names></name>
<name><surname>Garbers</surname>
<given-names>C. F.</given-names></name>
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Buttery</surname>
<given-names>R. G.</given-names></name>
<name><surname>Braude</surname>
<given-names>E. A.</given-names></name>
<name><surname>Evans</surname>
<given-names>E. A.</given-names></name>
<name><surname>Bunton</surname>
<given-names>C. A.</given-names></name>
<name><surname>Welch</surname>
<given-names>V. A.</given-names></name>
<name><surname>Buckley</surname>
<given-names>D.</given-names></name>
<name><surname>Gibson</surname>
<given-names>M. S.</given-names></name>
<name><surname>Bell</surname>
<given-names>F.</given-names></name>
<name><surname>Castells</surname>
<given-names>J.</given-names></name>
<name><surname>Fletcher</surname>
<given-names>G. A.</given-names></name>
<name><surname>Chatt</surname>
<given-names>J.</given-names></name>
<name><surname>Williams</surname>
<given-names>A. A.</given-names></name>
<name><surname>Wakkad</surname>
<given-names>(the late) S. E. S. El</given-names></name>
<name><surname>Rizk</surname>
<given-names>H. A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3224</fpage>
<lpage>3248</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003224">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003224">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>632. Studies on the Diels–Alder reaction. Part IV. Reduction products of &lt;i&gt;cis&lt;/i&gt;-&lt;i&gt;syn&lt;/i&gt;-1 : 4 : 5 : 6 : 12 : 13 : 14 : 15-octahydro-8-methoxy-1 : 4-dioxochrysene and their interrelation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003249</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robins</surname>
<given-names>P. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3249</fpage>
<lpage>3260</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>633. A new and specific aromatisation reaction. Part I. Direct conversion of &lt;i&gt;cis&lt;/i&gt;-&lt;i&gt;syn&lt;/i&gt;-1 : 2 : 3 : 4 : 5 : 6 : 12 : 13 : 14 : 15-decahydro-8-methoxy-1 : 4-dioxochrysene into 1-alkoxy-5 : 6 : 11 : 12-tetrahydro-8-methoxychrysenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003260</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robins</surname>
<given-names>P. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>James</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3260</fpage>
<lpage>3268</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003260">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003260">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>634. The hydrolysis of di&lt;i&gt;iso&lt;/i&gt;propyl methylphosphonodithiolate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>R. F.</given-names></name>
<name><surname>Keay</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3269</fpage>
<lpage>3271</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>635. Triterpenoids. Part LIII. The constitution and stereochemistry of butyrospermol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003272</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawrie</surname>
<given-names>William</given-names></name>
<name><surname>Hamilton</surname>
<given-names>William</given-names></name>
<name><surname>Spring</surname>
<given-names>F. S.</given-names></name>
<name><surname>Watson</surname>
<given-names>H. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3272</fpage>
<lpage>3280</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003272">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003272">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>636. Quassin and &lt;i&gt;neo&lt;/i&gt;quassin. Part VI</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003280</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beer</surname>
<given-names>R. J. S.</given-names></name>
<name><surname>Hanson</surname>
<given-names>K. R.</given-names></name>
<name><surname>Robertson</surname>
<given-names>Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3280</fpage>
<lpage>3284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003280">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003280">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>637. The interaction of boron trichloride with unsaturated alcohols and ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003285</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
<name><surname>Silver</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3285</fpage>
<lpage>3288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003285">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003285">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>638. Preparation of 1-oxygenated steroids. The reaction of cholest-1-en-3&lt;i&gt;β&lt;/i&gt;-ol with thionyl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003289</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Henbest</surname>
<given-names>H. B.</given-names></name>
<name><surname>Wilson</surname>
<given-names>R. A. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3289</fpage>
<lpage>3292</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003289">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003289">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>639. A search for new trypanocides. Part II. 4-Amino-6-dialkylaminoquinaldines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003293</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bader</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3293</fpage>
<lpage>3296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003293">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003293">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>640. Some reactions of hœmatoxylin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003296</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duff</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3296</fpage>
<lpage>3298</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003296">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003296">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>641. Kinetics and mechanism of hydrochlorination of the surface of rubber latex particles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003298</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gordon</surname>
<given-names>Manfred</given-names></name>
<name><surname>Carbarns</surname>
<given-names>Thomas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3298</fpage>
<lpage>3306</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003298">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003298">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>642. Statistical thermodynamic interpretation of the sorption of water and methanol by carbon</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003307</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barrer</surname>
<given-names>R. M.</given-names></name>
<name><surname>Stuart</surname>
<given-names>W. I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3307</fpage>
<lpage>3311</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003307">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003307">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>643. Pteridine derivatives. Part III. Bisdihydropurinyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fidler</surname>
<given-names>W. E.</given-names></name>
<name><surname>Wood</surname>
<given-names>H. C. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3311</fpage>
<lpage>3315</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>644. A new synthesis of 4-hydroxycoumarins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003315</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Garden</surname>
<given-names>J. F.</given-names></name>
<name><surname>Hayes</surname>
<given-names>N. F.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3315</fpage>
<lpage>3318</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003315">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003315">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>645. The formation of phenyl radicals from tetraphenyl-lead</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003319</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spice</surname>
<given-names>J. E.</given-names></name>
<name><surname>Twist</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3319</fpage>
<lpage>3323</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003319">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003319">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>646. The decomposition of mercury fulminate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003323</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bartlett</surname>
<given-names>B. E.</given-names></name>
<name><surname>Tompkins</surname>
<given-names>F. C.</given-names></name>
<name><surname>Young</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3323</fpage>
<lpage>3330</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003323">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003323">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>647. The decomposition of lead styphnate monohydrate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tompkins</surname>
<given-names>F. C.</given-names></name>
<name><surname>Young</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3331</fpage>
<lpage>3332</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>648. Alkenylation with lithium alkenyls. Part XIII. 1-Methylvinyl-lithium (&lt;i&gt;iso&lt;/i&gt;Propenyl-lithium)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003333</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Braude</surname>
<given-names>(the late) E. A.</given-names></name>
<name><surname>Evans</surname>
<given-names>E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3333</fpage>
<lpage>3337</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003333">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003333">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>649. The kinetics and mechanisms of addition to olefinic substances. Part III. The carbonium ionic intermediate involved in addition of hypochlorous acid to &lt;i&gt;iso&lt;/i&gt;butene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003337</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Salama</surname>
<given-names>Adib</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3337</fpage>
<lpage>3346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>650. The oxidation of derivatives of &lt;i&gt;o&lt;/i&gt;-phenylenediamine. Part IV. A new series of glyoxalinophenazines derived from anilino&lt;i&gt;apo&lt;/i&gt;safranines and their behaviour on hydrogenation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003347</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barry</surname>
<given-names>Vincent C.</given-names></name>
<name><surname>Belton</surname>
<given-names>J. G.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Twomey</surname>
<given-names>Dermot</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3347</fpage>
<lpage>3350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003347">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003347">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>651. Co-ordination complexes of methyl derivatives of indium and thallium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coates</surname>
<given-names>G. E.</given-names></name>
<name><surname>Whitcombe</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3351</fpage>
<lpage>3354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>652. The heat of hydrolysis of ethyl orthosilicate and of chlorotriethoxysilane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flitcroft</surname>
<given-names>T.</given-names></name>
<name><surname>Skinner</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3355</fpage>
<lpage>3358</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>653. The preparation and properties of some plutonium compounds. Part V. Colloidal quadrivalent plutonium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003358</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ockenden</surname>
<given-names>D. W.</given-names></name>
<name><surname>Welch</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3358</fpage>
<lpage>3363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003358">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003358">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>654. The absorption of uncharged molecules by ion-exchange resins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Reichenberg</surname>
<given-names>D.</given-names></name>
<name><surname>Wall</surname>
<given-names>W. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3364</fpage>
<lpage>3373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003364">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>655. Structure and reactivity of the oxy-anions of transition metals. Part I. The manganese oxy-anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carrington</surname>
<given-names>A.</given-names></name>
<name><surname>Symons</surname>
<given-names>M. C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3373</fpage>
<lpage>3380</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>656. Molecular-weight studies of dextran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Booth</surname>
<given-names>G. C.</given-names></name>
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3380</fpage>
<lpage>3385</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>657. The polonium halides. Part III. Polonium tetraiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003385</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bagnall</surname>
<given-names>K. W.</given-names></name>
<name><surname>D'Eye</surname>
<given-names>R. W. M.</given-names></name>
<name><surname>Freeman</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3385</fpage>
<lpage>3389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003385">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003385">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>658. The lupin alkaloids. Part XVI. The synthesis of externally compensated lupanine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003390</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clemo</surname>
<given-names>G. R.</given-names></name>
<name><surname>Raper</surname>
<given-names>R.</given-names></name>
<name><surname>Seaton</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3390</fpage>
<lpage>3394</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003390">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003390">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>659. The resolution of secondary and tertiary alcohols containing the pyridyl group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003394</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Kenyon</surname>
<given-names>J.</given-names></name>
<name><surname>Thaker</surname>
<given-names>Kumar</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3394</fpage>
<lpage>3397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003394">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003394">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>660. A conductivity method for the accurate determination of carbon in low-carbon steels</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003398</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dailly</surname>
<given-names>D. F.</given-names></name>
<name><surname>Elliott</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3398</fpage>
<lpage>3404</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003398">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003398">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>661. The thermal decomposition of oxamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003405</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tayler</surname>
<given-names>F. M.</given-names></name>
<name><surname>Bircumshaw</surname>
<given-names>L. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3405</fpage>
<lpage>3410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003405">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003405">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>662. The fate of methyl radicals in the mechanism of thermal decomposition of metal alkyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Long</surname>
<given-names>L. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3410</fpage>
<lpage>3416</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>663. Perfluoroalkyl derivatives of nitrogen. Part III. Heptafluoronitrosopropane, perfluoro-2-&lt;i&gt;n&lt;/i&gt;-propyl-1 : 2-oxazetidine, perfluoro-(methylene-&lt;i&gt;n&lt;/i&gt;-propylamine), and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003416</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barr</surname>
<given-names>D. A.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3416</fpage>
<lpage>3428</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003416">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003416">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>664. Perfluoroalkyl derivatives of nitrogen. Part IV. The synthesis, properties and infrared spectra of perfluoroalkyl &lt;i&gt;iso&lt;/i&gt;cyanates and carbamates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barr</surname>
<given-names>D. A.</given-names></name>
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3428</fpage>
<lpage>3435</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>665. Polynuclear heterocyclic systems. Part X. The elbs reaction with heterocyclic ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003435</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Christie</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3435</fpage>
<lpage>3437</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003435">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003435">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>666. Polynuclear heterocyclic systems. Part XI. Absorption spectra of compounds containing five-membered rings</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003438</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Christie</surname>
<given-names>B. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3438</fpage>
<lpage>3442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003438">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003438">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>667. Pteridine studies. Part IX. The structure of the monohydroxypteridines and their &lt;i&gt;N&lt;/i&gt;-methyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003443</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. J.</given-names></name>
<name><surname>Mason</surname>
<given-names>S. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3443</fpage>
<lpage>3453</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003443">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003443">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>668. The fluorination of tellurium. Ditellurium decafluoride and tellurium oxyfluorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003454</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>R.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3454</fpage>
<lpage>3458</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003454">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003454">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>669. Nucleotides. Part XXXVIII. An improved synthesis of uridine-diphosphate-glucose (UDPG)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003459</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Michelson</surname>
<given-names>A. M.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3459</fpage>
<lpage>3463</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003459">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003459">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>670. Dielectric properties of some aluminium soaps and of their solutions in toluene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nelson</surname>
<given-names>S. M.</given-names></name>
<name><surname>Gilmour</surname>
<given-names>A.</given-names></name>
<name><surname>Pink</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3463</fpage>
<lpage>3469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>671. Structural chemistry of the alkoxides. Part VII. Secondary alkoxides of quadrivalent cerium and thorium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Chatterjee</surname>
<given-names>A. K.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3469</fpage>
<lpage>3472</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>672. The reactivity of 2-bromopent-2-enoic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003472</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Alles</surname>
<given-names>B. J. P.</given-names></name>
<name><surname>Sultanbawa</surname>
<given-names>M. U. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3472</fpage>
<lpage>3474</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003472">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003472">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>673. Anomalies in the reduction of 2 : 2′-diacetyldiphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003475</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>D. Muriel</given-names></name>
<name><surname>Ladbury</surname>
<given-names>Joan E.</given-names></name>
<name><surname>Lesslie</surname>
<given-names>Mary S.</given-names></name>
<name><surname>Turner</surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3475</fpage>
<lpage>3482</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003475">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003475">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>674. The structure of the extracellular polysaccharide of &lt;i&gt;Aerobacter aerogenes&lt;/i&gt; A3 (S1)(Klebsiella Type 54)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003483</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Jamieson</surname>
<given-names>R. S. P.</given-names></name>
<name><surname>Wilkinson</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3483</fpage>
<lpage>3487</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003483">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003483">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>675. The synthesis of indeno[2,1-&lt;i&gt;a&lt;/i&gt;]perinaphthene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003487</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aitken</surname>
<given-names>I. M.</given-names></name>
<name><surname>Reid</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3487</fpage>
<lpage>3495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003487">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003487">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>676. 2-Acyl derivatives of cyclic 1 : 3-diones. Part III. Ultraviolet and infrared absorption spectra of 2-acylcyclohexane-1 : 3-diones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003495</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3495</fpage>
<lpage>3499</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003495">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003495">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>677. The 3-methylcholestanols and their derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003500</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Campos-Neves</surname>
<given-names>A. da S.</given-names></name>
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3500</fpage>
<lpage>3506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003500">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003500">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>678. The mechanisms of inhibition and retardation in radical polymerizations. Part III. The use of a stable free radical as an inhibitor</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003506</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevington</surname>
<given-names>J. C.</given-names></name>
<name><surname>Ghanem</surname>
<given-names>N. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3506</fpage>
<lpage>3509</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003506">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003506">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>679. Sulphanilamide derivatives: compounds derived from 2- and 4-aminoquinazoline and 1-aminophthalazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003509</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rodda</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3509</fpage>
<lpage>3512</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003509">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003509">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>680. The mechanism of the pinacol–pinacone rearrangement. Part I. Catalysis by strong monobasic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003512</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duncan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Lynn</surname>
<given-names>K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3512</fpage>
<lpage>3519</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003512">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003512">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>681. The mechanism of the pinacol–pinacone rearrangement. Part II. Catalysis by sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Duncan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Lynn</surname>
<given-names>K. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3519</fpage>
<lpage>3524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>682. Studies on phosphorylation. Part XIV. The solvolysis by phenols of benzyl phosphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
<name><surname>Mather</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3524</fpage>
<lpage>3531</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>683. Some aspects of the system uranium trioxide–water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003531</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dawson</surname>
<given-names>J. K.</given-names></name>
<name><surname>Wait</surname>
<given-names>E.</given-names></name>
<name><surname>Alcock</surname>
<given-names>K.</given-names></name>
<name><surname>Chilton</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3531</fpage>
<lpage>3540</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003531">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003531">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>684. Ethyl &lt;i&gt;p&lt;/i&gt;-nitrobenzoylethoxaloacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003541</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forrest</surname>
<given-names>J.</given-names></name>
<name><surname>Hansen</surname>
<given-names>S. B.</given-names></name>
<name><surname>Petrow</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3541</fpage>
<lpage>3545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003541">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003541">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>685. The chemistry of fungi. Part XXVI. Dechloronornidulin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003545</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dean</surname>
<given-names>F. M.</given-names></name>
<name><surname>Erni</surname>
<given-names>A. D. T.</given-names></name>
<name><surname>Robertson</surname>
<given-names>Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3545</fpage>
<lpage>3548</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>686. Molecular polarisability. The C–C, C–O, CO, C–Cl, C–Br, and C–I link polarisabilities, and the conformations of &lt;i&gt;cyclo&lt;/i&gt;pentane, of &lt;i&gt;cyclo&lt;/i&gt;hexyl chloride, bromide, and iodide, and of &lt;i&gt;cyclo&lt;/i&gt;pentanone, &lt;i&gt;cyclo&lt;/i&gt;hexanone, &lt;i&gt;cyclo&lt;/i&gt;hexane-1 : 4-dione, comphor, paraldehyde, and tetrahydrofuran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003549</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>(Mrs.) C. G. Le</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3549</fpage>
<lpage>3563</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003549">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003549">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>687. Studies in pyrolysis. Part VII. Model systems for the pyrolysis of poly(ethylene terephthalate): 2 : 2′-dibenzoyloxydiethyl ether, 2′benzoyloxyethyl vinyl ether, and certain related vinyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003563</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Iengar</surname>
<given-names>H. V. R.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3563</fpage>
<lpage>3570</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003563">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003563">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>688. Electrophilic substitution. Part III. The nitration of phenanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003570</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Warford</surname>
<given-names>E. W. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3570</fpage>
<lpage>3572</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003570">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003570">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>689. Electrophilic substitution. Part IV. The nitration of diphenyl, chrysene, benzo[&lt;i&gt;a&lt;/i&gt;]pyrene, and anthanthrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003572</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Mole</surname>
<given-names>T.</given-names></name>
<name><surname>Urch</surname>
<given-names>D. S.</given-names></name>
<name><surname>Warford</surname>
<given-names>E. W. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3572</fpage>
<lpage>3575</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>690. Electrophilic substitution. Part V. Competitive nitrations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003576</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Mole</surname>
<given-names>T.</given-names></name>
<name><surname>Warford</surname>
<given-names>E. W. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3576</fpage>
<lpage>3580</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003576">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003576">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>691. Electrophilic substitution. Part VI. The nitration of aromatic hydrocarbons; partial rate factors and their interpretation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003581</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dewar</surname>
<given-names>M. J. S.</given-names></name>
<name><surname>Mole</surname>
<given-names>T.</given-names></name>
<name><surname>Warford</surname>
<given-names>E. W. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3581</fpage>
<lpage>3586</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003581">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003581">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>692. The crystal and molecular structure of pteridine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003586</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hamor</surname>
<given-names>T. A.</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3586</fpage>
<lpage>3594</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003586">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003586">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>693. Calculated bond lengths in some cyclic compounds. Part IV. Pteridine and melamine, and a correlation curve for C–N bonds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003595</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodwin</surname>
<given-names>T. H.</given-names></name>
<name><surname>Porte</surname>
<given-names>A. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3595</fpage>
<lpage>3599</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>694. Peri-hydroxycarbonyl compounds. Part II. The effect of ring size on hydrogen bonding</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003600</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Farmer</surname>
<given-names>V. C.</given-names></name>
<name><surname>Hayes</surname>
<given-names>N. F.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3600</fpage>
<lpage>3607</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003600">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003600">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>695. Lactones. Part III. A further example of alkyl–oxygen bond fission in phthalide ring opening</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003608</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blair</surname>
<given-names>John</given-names></name>
<name><surname>Logan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Newbold</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3608</fpage>
<lpage>3612</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003608">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003608">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>696. The preparation of active solids by thermal decomposition. Part IX. The calcination of hydrous ferric oxide and of lepidocrocite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003612</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodman</surname>
<given-names>J. F.</given-names></name>
<name><surname>Gregg</surname>
<given-names>S. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3612</fpage>
<lpage>3620</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003612">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003612">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>697. Physical properties and chemical constitution. Part XXV. (&lt;i&gt;A&lt;/i&gt;) determination of the orientation polarization of alkylpyridines in benzene solutions by two independent methods. (&lt;i&gt;b&lt;/i&gt;) dipole moments of alkylpyridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Vogel</surname>
<given-names>A. I.</given-names></name>
<name><surname>Walker</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3621</fpage>
<lpage>3628</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>698. The kinetics of alkyl–oxygen fission in ester hydrolysis. Part V. Diphenylmethyl esters in aqueous acetone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harvey</surname>
<given-names>G. J.</given-names></name>
<name><surname>Stimson</surname>
<given-names>V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3629</fpage>
<lpage>3631</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>699. Radical exchange in organometallic compounds. Part I. The replacement of methyl by trifluoromethyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haszeldine</surname>
<given-names>R. N.</given-names></name>
<name><surname>West</surname>
<given-names>B. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3631</fpage>
<lpage>3637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>700. Fluorine-substituted polycyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003637</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Badger</surname>
<given-names>G. M.</given-names></name>
<name><surname>Stephens</surname>
<given-names>J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3637</fpage>
<lpage>3640</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003637">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003637">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>701. The formation of &lt;i&gt;iso&lt;/i&gt;but-1-enyl radicals from &lt;i&gt;iso&lt;/i&gt;but-1-enylsilver. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003640</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Glockling</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3640</fpage>
<lpage>3642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003640">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003640">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>702. Polypeptides. Part IV. The self-condensation of the esters of some peptides of glycine and proline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
<name><surname>Smith</surname>
<given-names>P. W. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3642</fpage>
<lpage>3650</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>703. Possible ƒ-orbital hybridization in uranyl and related complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003650</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coulson</surname>
<given-names>C. A.</given-names></name>
<name><surname>Lester</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3650</fpage>
<lpage>3659</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003650">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003650">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>704. The structure of N&lt;sub&gt;&lt;i&gt;β&lt;/i&gt;&lt;/sub&gt;-alkyl-&lt;i&gt;β&lt;/i&gt;-carboline anhydro-bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003659</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spenser</surname>
<given-names>Ian D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3659</fpage>
<lpage>3663</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003659">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003659">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>705. Synthesis of heterocyclic compounds from &lt;i&gt;δ&lt;/i&gt;-unsaturated 1 : 3-diketo-esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003663</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Soliman</surname>
<given-names>Gabra</given-names></name>
<name><surname>Rateb</surname>
<given-names>Latif</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3663</fpage>
<lpage>3668</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003663">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003663">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>706. Diaryl-2 : 2′-disulphonic acids and related compounds. Part II. The optical stability of a cyclic 2 : 2′-thiolsulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003668</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Turner</surname>
<given-names>E. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3668</fpage>
<lpage>3673</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003668">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003668">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003674</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>D. Muriel</given-names></name>
<name><surname>Duncan</surname>
<given-names>J. F.</given-names></name>
<name><surname>Lynn</surname>
<given-names>K. R.</given-names></name>
<name><surname>Bird</surname>
<given-names>C. W.</given-names></name>
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Dandegaonker</surname>
<given-names>S. H.</given-names></name>
<name><surname>Watson</surname>
<given-names>J. S.</given-names></name>
<name><surname>Hargreaves</surname>
<given-names>M. K.</given-names></name>
<name><surname>Hetherington</surname>
<given-names>G.</given-names></name>
<name><surname>Robinson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Enslin</surname>
<given-names>P. R.</given-names></name>
<name><surname>Rivett</surname>
<given-names>D. E. A.</given-names></name>
<name><surname>Brown</surname>
<given-names>R. D.</given-names></name>
<name><surname>Heffernan</surname>
<given-names>M. L.</given-names></name>
<name><surname>Rees</surname>
<given-names>C. W.</given-names></name>
<name><surname>Newlands</surname>
<given-names>M. J.</given-names></name>
<name><surname>Wild</surname>
<given-names>F.</given-names></name>
<name><surname>Mare</surname>
<given-names>P. B. D. de la</given-names></name>
<name><surname>Leffek</surname>
<given-names>K.</given-names></name>
<name><surname>Salama</surname>
<given-names>Adib</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3674</fpage>
<lpage>3688</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003674">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003674">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Recent progress in the chemistry of peptides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003689</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kenner</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3689</fpage>
<lpage>3700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003689">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003689">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>718. Synthesis of lapachenole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003701</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Livingstone</surname>
<given-names>R.</given-names></name>
<name><surname>Watson</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3701</fpage>
<lpage>3704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003701">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003701">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>719. Infrared spectra and polar effects. Part IV. Steric restrictions of polar effects and their application in studies on rotational isomerism</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003704</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellamy</surname>
<given-names>L. J.</given-names></name>
<name><surname>Thomas</surname>
<given-names>L. C.</given-names></name>
<name><surname>Williams</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3704</fpage>
<lpage>3708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003704">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003704">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>720. Thermodynamics of hydrocarbon mixtures. Part II. The heats of mixing of the binary mixtures formed by benzene, &lt;i&gt;cyclo&lt;/i&gt;hexane, &lt;i&gt;n&lt;/i&gt;-heptane, toluene, and &lt;i&gt;n&lt;/i&gt;-hexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003708</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mathieson</surname>
<given-names>A. R.</given-names></name>
<name><surname>Thynne</surname>
<given-names>J. C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3708</fpage>
<lpage>3713</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003708">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003708">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>721. Thermodynamics of hydrocarbon mixtures. Part III. The heats of mixing of ternary, quaternary, and quinary mixtures formed by benzene, &lt;i&gt;cyclo&lt;/i&gt;hexane, heptane, toluene, and hexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003713</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mathieson</surname>
<given-names>A. R.</given-names></name>
<name><surname>Thynne</surname>
<given-names>J. C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3713</fpage>
<lpage>3716</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003713">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003713">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>722. Studies in relation to biosynthesis. Part VIII. The structure of mycelianamide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003717</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Massy-Westropp</surname>
<given-names>R. A.</given-names></name>
<name><surname>Rickards</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3717</fpage>
<lpage>3721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003717">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003717">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>723. Raman spectrum of the tetrachlorogallate ion (GaCl&lt;sub&gt;4&lt;/sub&gt;&lt;sup&gt;–&lt;/sup&gt;) in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Woodward</surname>
<given-names>L. A.</given-names></name>
<name><surname>Nord</surname>
<given-names>A. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3721</fpage>
<lpage>3722</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003721">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>724. Raman spectrum and constitution of fused gallium dichloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003723</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Woodward</surname>
<given-names>L. A.</given-names></name>
<name><surname>Garton</surname>
<given-names>G.</given-names></name>
<name><surname>Roberts</surname>
<given-names>H. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3723</fpage>
<lpage>3725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003723">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003723">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>725. The surface chemistry of germanium. Part I. Chemical effects at &lt;i&gt;pn&lt;/i&gt; junctions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003726</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carasso</surname>
<given-names>J. I.</given-names></name>
<name><surname>Stelzer</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3726</fpage>
<lpage>3732</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003726">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003726">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>726. The mesomorphic behaviour of the fatty esters of cholesterol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003733</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gray</surname>
<given-names>G. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3733</fpage>
<lpage>3739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003733">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003733">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>727. A search for new trypanocides. Part III. Some analogues of suramin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adams</surname>
<given-names>A.</given-names></name>
<name><surname>Ashley</surname>
<given-names>J. N.</given-names></name>
<name><surname>Bader</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3739</fpage>
<lpage>3744</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003739">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>728. The constitution of a xylan from norway spruce (&lt;i&gt;Picea excelsa&lt;/i&gt;)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003744</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Carter</surname>
<given-names>(Miss) Mary E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3744</fpage>
<lpage>3748</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003744">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003744">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>729. The constitution of conessine. Part IX. Further studies with steroidal amines related to conessine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003749</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haworth</surname>
<given-names>R. D.</given-names></name>
<name><surname>Lunts</surname>
<given-names>L. H. C.</given-names></name>
<name><surname>McKenna</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3749</fpage>
<lpage>3752</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003749">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003749">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>730. The distribution of ester groups in dextran sulphate and their stability towards hydrolytic reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003752</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ricketts</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3752</fpage>
<lpage>3756</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003752">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003752">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>731. Transport to the surface of a rotating disc</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>D. P.</given-names></name>
<name><surname>Riddiford</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3756</fpage>
<lpage>3764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>732. The viscosity and intermolecular potential of silicon tetrafluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003765</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ellis</surname>
<given-names>C. P.</given-names></name>
<name><surname>Raw</surname>
<given-names>C. J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3765</fpage>
<lpage>3766</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003765">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003765">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>733. Chemistry of the higher fungi. Part VI. Isomerisation reactions of naturally occurring allenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003767</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bu'Lock</surname>
<given-names>J. D.</given-names></name>
<name><surname>Jones</surname>
<given-names>E. R. H.</given-names></name>
<name><surname>Leeming</surname>
<given-names>P. R.</given-names></name>
<name><surname>Thompson</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3767</fpage>
<lpage>3771</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003767">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003767">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>734. Chemical action of ionising radiations in solutions. Part XVI. Formation of labile phosphate esters from purine and pyrimidine ribonucleotides by irradiation with &lt;i&gt;X&lt;/i&gt;-rays in aqueous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003771</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Daniels</surname>
<given-names>M.</given-names></name>
<name><surname>Scholes</surname>
<given-names>G.</given-names></name>
<name><surname>Weiss</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3771</fpage>
<lpage>3779</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003771">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003771">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>735. Steric effects in electronic spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Murrell</surname>
<given-names>J. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3779</fpage>
<lpage>3784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>736. The preparation of uniformly &lt;sup&gt;14&lt;/sup&gt;C-labelled substances on a laboratory scale, with special reference to L-tryptophan</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003784</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dalgliesh</surname>
<given-names>C. E.</given-names></name>
<name><surname>Dutton</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3784</fpage>
<lpage>3791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003784">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003784">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>737. An apparatus for preparative photosynthesis of &lt;sup&gt;14&lt;/sup&gt;C-labelled substances</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003792</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dutton</surname>
<given-names>R. W.</given-names></name>
<name><surname>Dalgliesh</surname>
<given-names>C. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3792</fpage>
<lpage>3796</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003792">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003792">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>738. The effects of substituents on the rates of hydrolysis of some organophosphorus compounds. Part I. Rates in alkaline solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003796</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heath</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3796</fpage>
<lpage>3804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003796">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003796">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>739. The effects of substituents on the rates of hydrolysis of some organophosphorus compounds. Part II. Rates in neutral solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003804</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heath</surname>
<given-names>D. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3804</fpage>
<lpage>3809</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003804">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003804">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>740. Vibrational frequency correlations in heterocyclic molecules. Part II. Infrared spectra and structure of oxindole and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003809</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kellie</surname>
<given-names>A. E.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>D. G.</given-names></name>
<name><surname>Sadler</surname>
<given-names>P. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3809</fpage>
<lpage>3813</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003809">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003809">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>741. Studies in peroxidase action. Part XI. The oxidation of a mixture of amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hughes</surname>
<given-names>G. M. K.</given-names></name>
<name><surname>Saunders</surname>
<given-names>B. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3814</fpage>
<lpage>3820</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>742. Synthetic and oxidative studies in the polyhydroxydiphenyl series. Part II. 5 : 6-Dichloro-2 : 3-Dihydroxydiphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003820</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bruce</surname>
<given-names>J. Malcolm</given-names></name>
<name><surname>Sutcliffe</surname>
<given-names>F. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3820</fpage>
<lpage>3823</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003820">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003820">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>743. Synthetic and oxidative studies in the polyhydroxydiphenyl series. Part III. 2 : 3-Dihydroxy-5 : 6-dimethyldiphenyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003824</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bruce</surname>
<given-names>J. Malcolm</given-names></name>
<name><surname>Sutcliffe</surname>
<given-names>F. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3824</fpage>
<lpage>3829</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003824">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003824">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>744. The constitution of a wheat-straw hemicellulose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003830</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Meek</surname>
<given-names>Eric G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3830</fpage>
<lpage>3834</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003830">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003830">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>745. A new synthesis of 3-hydroxy-1 : 2-benzofluorene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003834</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>Neil</given-names></name>
<name><surname>Ciganek</surname>
<given-names>Engelbert</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3834</fpage>
<lpage>3836</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003834">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003834">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>746. Magnetic studies with copper(II) salts. Part I. Anomalous paramagnetism and &lt;i&gt;δ&lt;/i&gt;-bonding in anhydrous and hydrated copper(II) acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003837</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Figgis</surname>
<given-names>B. N.</given-names></name>
<name><surname>Martin</surname>
<given-names>R. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3837</fpage>
<lpage>3846</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003837">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003837">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>747. Purines, pyrimidines, and glyoxalines. Part III. A new synthesis of 2-thiouracils</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003847</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>M. R.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
<name><surname>Schaffner</surname>
<given-names>K.</given-names></name>
<name><surname>Warrener</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3847</fpage>
<lpage>3849</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003847">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003847">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>748. Solutions in sulphuric acid. Part XX. Cryoscopic measurements on some aromatic sulphides, sulphoxides, and sulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003850</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gillespie</surname>
<given-names>R. J.</given-names></name>
<name><surname>Passerini</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3850</fpage>
<lpage>3854</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003850">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003850">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>749. The thermal decomposition of &lt;i&gt;cyclo&lt;/i&gt;pentyl bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Price</surname>
<given-names>S. J. W.</given-names></name>
<name><surname>Shaw</surname>
<given-names>R.</given-names></name>
<name><surname>Trotman-Dickenson</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3855</fpage>
<lpage>3857</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>750. Intramolecular acylation. Part I. Ring closure of some &lt;i&gt;β&lt;/i&gt;-(7-alkyl-1-naphthyl)propionic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003857</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wenham</surname>
<given-names>A. J. M.</given-names></name>
<name><surname>Whitehurst</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3857</fpage>
<lpage>3863</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003857">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003857">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>751. &lt;i&gt;Aconitum&lt;/i&gt; and &lt;i&gt;delphinium&lt;/i&gt; alkaloids. Part III. Some rearrangements in the delpheline and lycoctonine series. A monobasic dicarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003864</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Trevett</surname>
<given-names>M. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3864</fpage>
<lpage>3869</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003864">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003864">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>752. Nuclear-resonance spectra and the structures of the mono- and di-hydrate of boron trifluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003870</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ford</surname>
<given-names>P. T.</given-names></name>
<name><surname>Richards</surname>
<given-names>R. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3870</fpage>
<lpage>3874</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003870">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003870">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>753. 3 : 4-5 : 6-10 : 11-12 : 13-Tetrabenzoperopyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003875</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clar</surname>
<given-names>E.</given-names></name>
<name><surname>Kelly</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3875</fpage>
<lpage>3877</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003875">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003875">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>754. Circumanthracene and dinaphtho(7′ : 1′-1 : 13)(1″ : 7″-6 : 8)-peropyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003878</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clar</surname>
<given-names>E.</given-names></name>
<name><surname>Kelly</surname>
<given-names>W.</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
<name><surname>Rossmann</surname>
<given-names>M. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3878</fpage>
<lpage>3881</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003878">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003878">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>755. Interaction of Lewis acids with aromatic hydrocarbons and bases. Part XVII. The association of hexamethylbenzene with substituted &lt;i&gt;p&lt;/i&gt;-benzoquinones in carbon tetrachloride solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003881</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foster</surname>
<given-names>R.</given-names></name>
<name><surname>Hammick</surname>
<given-names>D. Ll.</given-names></name>
<name><surname>Placito</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3881</fpage>
<lpage>3887</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003881">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003881">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>756. The reaction of oximes with &lt;i&gt;iso&lt;/i&gt;propyl methylphosphono-fluoridate (Sarin)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003887</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Green</surname>
<given-names>A. L.</given-names></name>
<name><surname>Saville</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3887</fpage>
<lpage>3892</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003887">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003887">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>757. Antituberculosis agents. Part II. Dehydrobromination products and related bases derived from bis-2 : 3-dibromopropyl sulphide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003892</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Edwards</surname>
<given-names>D.</given-names></name>
<name><surname>Stenlake</surname>
<given-names>J. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3892</fpage>
<lpage>3900</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003892">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003892">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>758. The rates of reaction of copper, zinc, and uranium with organic solvent–dinitrogen tetroxide mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003900</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Addison</surname>
<given-names>C. C.</given-names></name>
<name><surname>Sheldon</surname>
<given-names>J. C.</given-names></name>
<name><surname>Hodge</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3900</fpage>
<lpage>3911</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003900">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003900">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>759. The kinetics of hydrogen isotope exchange reactions. Part VI. The reactivity of anisole in aqueous and non-aqueous acidic media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003911</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3911</fpage>
<lpage>3918</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003911">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003911">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>760. The dissociation pressure of cadmium oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003919</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilbert</surname>
<given-names>I. G. F.</given-names></name>
<name><surname>Kitchener</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3919</fpage>
<lpage>3921</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003919">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003919">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>761. The free energy of formation of zinc aluminate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003922</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilbert</surname>
<given-names>I. G. F.</given-names></name>
<name><surname>Kitchener</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3922</fpage>
<lpage>3924</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003922">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003922">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>762. The free energy of formation of zinc ferrite</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003924</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilbert</surname>
<given-names>I. G. F.</given-names></name>
<name><surname>Kitchener</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3924</fpage>
<lpage>3926</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003924">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003924">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>763. Phthalazines. Part I. Re-investigation of the preparation of phthalazines by cyclodehydration of acylhydrazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003927</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rodda</surname>
<given-names>H. J.</given-names></name>
<name><surname>Rogasch</surname>
<given-names>P. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3927</fpage>
<lpage>3929</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003927">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003927">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>764. The thermal degradation of polymethacrylonitrile. Part I. Separation of coloration and depolymerization reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003929</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grassie</surname>
<given-names>N.</given-names></name>
<name><surname>McNeill</surname>
<given-names>I. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3929</fpage>
<lpage>3933</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003929">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003929">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>765. Acylation and allied reactions catalysed by strong acids. Part XV. Some reactions of simple alkyl perchlorates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003933</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burton</surname>
<given-names>H.</given-names></name>
<name><surname>Munday</surname>
<given-names>D. A.</given-names></name>
<name><surname>Praill</surname>
<given-names>P. F. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3933</fpage>
<lpage>3939</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003933">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003933">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>766. The halogenation of phenolic ethers and anilides. Part XVIII. A kinetic method for the determination of the &lt;i&gt;ortho&lt;/i&gt;/&lt;i&gt;para&lt;/i&gt;-ratios for aromatic ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003939</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>Brynmor</given-names></name>
<name><surname>Richardson</surname>
<given-names>Eileen N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3939</fpage>
<lpage>3941</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003939">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003939">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>767. Bisquaternary ammonium salts. Part II. Salts of 4 : 4′-diaminostilbene-2 : 2′-disulphonic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003941</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Leeds</surname>
<given-names>W. G.</given-names></name>
<name><surname>Slack</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3941</fpage>
<lpage>3944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003941">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003941">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>768. The strengths of arylmethanols as secondary bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003944</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3944</fpage>
<lpage>3948</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003944">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003944">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>769. Magnetic properties of some metal carboxylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003948</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Herron</surname>
<given-names>R. C.</given-names></name>
<name><surname>Pink</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3948</fpage>
<lpage>3952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003948">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003948">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>770. The gum component of olibanum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003953</article-id><contrib-group><contrib contrib-type="author">
<name><surname>El-Khadem</surname>
<given-names>H.</given-names></name>
<name><surname>Megahed</surname>
<given-names>M. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3953</fpage>
<lpage>3958</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003953">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003953">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>771. A kinetic study of the alkaline hydrolysis of some aliphatic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003958</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thomas</surname>
<given-names>J. D. R.</given-names></name>
<name><surname>Watson</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3958</fpage>
<lpage>3963</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003958">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003958">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>772. Experiments on the synthesis of the pyrethrins. Part XI. Synthesis of &lt;i&gt;cis&lt;/i&gt;-pyrethrolone and pyrethrin I: introduction of the &lt;i&gt;cis&lt;/i&gt;-penta-2 : 4-dienyl system by selective hydrogenation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003963</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crombie</surname>
<given-names>L.</given-names></name>
<name><surname>Harper</surname>
<given-names>S. H.</given-names></name>
<name><surname>Newman</surname>
<given-names>F. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3963</fpage>
<lpage>3971</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003963">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003963">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>773. Oxidation by nitrous and nitric acid. Part IV. Spectroscopic investigation of the equilibrium between NO&lt;sup&gt;+&lt;/sup&gt; and nitrous acid in aqueous perchloric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003971</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Singer</surname>
<given-names>K.</given-names></name>
<name><surname>Vamplew</surname>
<given-names>(Miss) P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3971</fpage>
<lpage>3974</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003971">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003971">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003975</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ishay</surname>
<given-names>David B.</given-names></name>
<name><surname>Wright</surname>
<given-names>Winifred G.</given-names></name>
<name><surname>Ellis</surname>
<given-names>Peter</given-names></name>
<name><surname>Wilkins</surname>
<given-names>R. G.</given-names></name>
<name><surname>Williams</surname>
<given-names>M. J. G.</given-names></name>
<name><surname>Osborn</surname>
<given-names>A. R.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Schwarz</surname>
<given-names>J. C. P.</given-names></name>
<name><surname>Finnegan</surname>
<given-names>Maureen</given-names></name>
<name><surname>Davis</surname>
<given-names>M.</given-names></name>
<name><surname>Balenović</surname>
<given-names>K.</given-names></name>
<name><surname>Bregant</surname>
<given-names>N.</given-names></name>
<name><surname>Cerar</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3975</fpage>
<lpage>3984</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003975">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003975">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Obituary notice</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003985</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3985</fpage>
<lpage>3985</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003985">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003985">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of radicals in gaseous systems</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003986</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Steacie</surname>
<given-names>E. W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3986</fpage>
<lpage>3996</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003986">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003986">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Personal reminiscences of a radiochemist</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560003997</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hahn</surname>
<given-names>Otto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>3997</fpage>
<lpage>4003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560003997">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560003997">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Presidential address. Alkoxides old and new</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004004</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wardlaw C.B.E</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4004</fpage>
<lpage>4014</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004004">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004004">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>One Hundred and Fifteenth Annual General Meeting</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004015</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4015</fpage>
<lpage>4047</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004015">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>781. Unsaturated fatty acids. Part II. The synthesis of linolenic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004049</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nigam</surname>
<given-names>S. S.</given-names></name>
<name><surname>Weedon</surname>
<given-names>B. C. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4049</fpage>
<lpage>4054</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004049">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004049">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>782. The dimerisation of mesityl oxide. A novel type of diene addition</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004054</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Braude</surname>
<given-names>(the late) E. A.</given-names></name>
<name><surname>Gofton</surname>
<given-names>B. F.</given-names></name>
<name><surname>Lowe</surname>
<given-names>G.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4054</fpage>
<lpage>4060</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004054">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004054">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>783. Calciferol and its relatives. Part II. An alternative synthesis of &lt;i&gt;trans&lt;/i&gt;-1-2′-&lt;i&gt;cyclo&lt;/i&gt;hexylidene-ethylidene-2-methylene&lt;i&gt;cyclo&lt;/i&gt;hexane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004060</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lythgoe</surname>
<given-names>B.</given-names></name>
<name><surname>Trippett</surname>
<given-names>S.</given-names></name>
<name><surname>Watkins</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4060</fpage>
<lpage>4065</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004060">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004060">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>784. Synthesis of cystinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004066</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crawhall</surname>
<given-names>J. C.</given-names></name>
<name><surname>Elliott</surname>
<given-names>D. F.</given-names></name>
<name><surname>Hooper</surname>
<given-names>K. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4066</fpage>
<lpage>4068</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004066">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004066">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>785. The synthesis of (±)-angustione and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ensor</surname>
<given-names>G. R.</given-names></name>
<name><surname>Wilson</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4068</fpage>
<lpage>4073</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>786. Researches on acetylenic compounds. Part LII. The preparation and anomalous absorption spectra of some &lt;i&gt;bicyclo&lt;/i&gt;[2 : 2 : 1]-heptane derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004073</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>E. R. H.</given-names></name>
<name><surname>Mansfield</surname>
<given-names>G. H.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4073</fpage>
<lpage>4082</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004073">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004073">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>787. Researches on polyenes. Part IV. The ω-&lt;i&gt;p&lt;/i&gt;-methoxyphenyl-polyene aldehydes and their absorption spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004082</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marshall</surname>
<given-names>D.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4082</fpage>
<lpage>4088</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004082">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004082">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>788. Some new analogues of pethidine. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004088</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>R. J.</given-names></name>
<name><surname>Frearson</surname>
<given-names>P. M.</given-names></name>
<name><surname>Stern</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4088</fpage>
<lpage>4091</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004088">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004088">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>789. Colouring matters of the aphididœ. Part XV. The alkaline inversion of erythroaphin-&lt;i&gt;sl&lt;/i&gt; and its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004091</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>A. W.</given-names></name>
<name><surname>Todd</surname>
<given-names>Sir Alexander R.</given-names></name>
<name><surname>Watkins</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4091</fpage>
<lpage>4093</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004091">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004091">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>790. The alleged occurrence of vitamin A in baker's yeast</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004094</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Heaton</surname>
<given-names>F. W.</given-names></name>
<name><surname>Lowe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Morton</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4094</fpage>
<lpage>4095</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004094">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004094">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>791. Elaboration products of eucarvone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004096</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>J. R. B.</given-names></name>
<name><surname>Islam</surname>
<given-names>A. M.</given-names></name>
<name><surname>Raphael</surname>
<given-names>R. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4096</fpage>
<lpage>4103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004096">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004096">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>792. Tetronic acids and related compounds. Part I. Synthesis from α-hydroxy-esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004103</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
<name><surname>Stanners</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4103</fpage>
<lpage>4106</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004103">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004103">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>793. The preparation of 4-amino- and other pteridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004106</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>R. M.</given-names></name>
<name><surname>Jones</surname>
<given-names>P. G.</given-names></name>
<name><surname>Palmer</surname>
<given-names>P. J.</given-names></name>
<name><surname>Stephens</surname>
<given-names>F. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4106</fpage>
<lpage>4113</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004106">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004106">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>794. Potential thiophen chemotherapeutics. Part V. Preparation and proof of structure of some substituted 5-aminothiophen-2-sulphonamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004114</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cymerman-Craig</surname>
<given-names>J.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>G. N.</given-names></name>
<name><surname>Warburton</surname>
<given-names>W. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4114</fpage>
<lpage>4118</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004114">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004114">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>795. Purines, pyrimidines, and glyoxalines. Part IV. Cyanouracils from amines and amino-acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004118</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Atkinson</surname>
<given-names>M. R.</given-names></name>
<name><surname>Shaw</surname>
<given-names>G.</given-names></name>
<name><surname>Warrener</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4118</fpage>
<lpage>4123</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004118">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004118">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>796. The aporphine series. Part II. Application of the Bischler–Napieralski reaction to 2-nitrophenyl-&lt;i&gt;N&lt;/i&gt;-phenethylacetamides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004123</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Palluel</surname>
<given-names>A. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4123</fpage>
<lpage>4129</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004123">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004123">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>797. Pulcherrimin : a synthesis of 1 : 4-dihydroxy-2 : 5-dioxopiperazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004130</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>A. H.</given-names></name>
<name><surname>Slater</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4130</fpage>
<lpage>4133</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004130">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004130">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>798. The structure of pulcherrimin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004133</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>A. H.</given-names></name>
<name><surname>Slater</surname>
<given-names>C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4133</fpage>
<lpage>4135</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004133">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004133">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>799. Heterocyclic imines and amines. Part VII. &lt;i&gt;N&lt;/i&gt;-substituted phthalic imidine derivatives and their reactions with amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004135</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Clark</surname>
<given-names>P. F.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Golden</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4135</fpage>
<lpage>4143</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004135">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004135">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>800. Compounds containing directly linked pyrrole rings. Part II. Dialkylimino-β-&lt;i&gt;iso&lt;/i&gt;indigos</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004144</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
<name><surname>Golden</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4144</fpage>
<lpage>4150</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004144">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004144">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>801. Triterpenoids. Part XXII. The constitution and stereochemistry of masticadienonic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004150</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Seoane</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4150</fpage>
<lpage>4157</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004150">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004150">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>802. Further crystalline constituents of gum mastic</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004158</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Seoane</surname>
<given-names>Eliseo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4158</fpage>
<lpage>4160</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004158">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004158">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>803. Triterpenoids. Part XXIII. The nature of lantadene A</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004160</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barton</surname>
<given-names>D. H. R.</given-names></name>
<name><surname>Mayo</surname>
<given-names>P. de</given-names></name>
<name><surname>Orr</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4160</fpage>
<lpage>4162</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004160">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004160">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>804. The constituents of &lt;i&gt;Casimiroa edulis&lt;/i&gt; llave &lt;i&gt;et&lt;/i&gt; lex. Part I. The seed</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kincl</surname>
<given-names>F. A.</given-names></name>
<name><surname>Romo</surname>
<given-names>J.</given-names></name>
<name><surname>Rosenkranz</surname>
<given-names>G.</given-names></name>
<name><surname>Sondheimer</surname>
<given-names>Franz</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4163</fpage>
<lpage>4169</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>805. The constituents of &lt;i&gt;Casimiroa edulis&lt;/i&gt; llave &lt;i&gt;et&lt;/i&gt; lex. Part II. The bark</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004170</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Iriarte</surname>
<given-names>J.</given-names></name>
<name><surname>Kincl</surname>
<given-names>F. A.</given-names></name>
<name><surname>Rosenkranz</surname>
<given-names>G.</given-names></name>
<name><surname>Sondheimer</surname>
<given-names>Franz</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4170</fpage>
<lpage>4173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004170">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004170">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>806. Syntheses in the quinazolone series. Part II. Synthesis of quino- and quinazo-quinazolones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stephen</surname>
<given-names>(Mrs.) T.</given-names></name>
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4173</fpage>
<lpage>4177</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>807. Syntheses in the quinazolone series. Part III. The formation of quinazo[4,3-&lt;i&gt;b&lt;/i&gt;]quinazol-8-one and 2-&lt;i&gt;o&lt;/i&gt;-aminophenylquinazol-4-one by the hydrolysis of 3-4′-quinazolinylquinazol-4-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004178</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stephen</surname>
<given-names>(Mrs.) T.</given-names></name>
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4178</fpage>
<lpage>4180</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004178">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004178">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>808. The polarography of oximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004180</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gardner</surname>
<given-names>H. J.</given-names></name>
<name><surname>Georgans</surname>
<given-names>W. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4180</fpage>
<lpage>4186</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004180">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004180">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>809. Cytidine diphosphate glycerol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004186</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddiley</surname>
<given-names>J.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Mathias</surname>
<given-names>A. P.</given-names></name>
<name><surname>Sanderson</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4186</fpage>
<lpage>4190</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004186">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004186">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>810. Studies of the amino-&lt;i&gt;iso&lt;/i&gt;quinolines, -cinnolines, and -quinazolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004191</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Osborn</surname>
<given-names>A. R.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Short</surname>
<given-names>L. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4191</fpage>
<lpage>4206</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004191">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004191">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>811. Cinnolines. Part XXXV. Studies of the chloro- and hydroxy-cinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004207</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Osborn</surname>
<given-names>A. R.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4207</fpage>
<lpage>4213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004207">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004207">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>812. The synthesis of 3 : 4- and 5 : 6-benzophenanthridines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mills</surname>
<given-names>B.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4213</fpage>
<lpage>4224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>813. Flavogallol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004225</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
<name><surname>Haworth</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4225</fpage>
<lpage>4232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004225">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004225">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>814. Some experiments with &lt;i&gt;cyclo&lt;/i&gt;pentanones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004232</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4232</fpage>
<lpage>4237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004232">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004232">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>815. Some degradation products of fumagillin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004237</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Landquist</surname>
<given-names>Justus K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4237</fpage>
<lpage>4245</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004237">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004237">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>816. Organic sulphur compounds. Part I. The structure of anthra-9 : 10-quinone-1-sulphenic acid, its derivatives, and analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004245</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barltrop</surname>
<given-names>J. A.</given-names></name>
<name><surname>Morgan</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4245</fpage>
<lpage>4251</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004245">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004245">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>817. Some derivatives of 2 : 3-dihydroxynaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004252</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howell</surname>
<given-names>F. H.</given-names></name>
<name><surname>Taylor</surname>
<given-names>D. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4252</fpage>
<lpage>4256</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004252">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004252">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>818. Aromatic substitution. Part II. Nitration of aromatic compounds with nitronium tetrafluoroborate and other stable nitronium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004257</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oláh</surname>
<given-names>G.</given-names></name>
<name><surname>Kuhn</surname>
<given-names>S.</given-names></name>
<name><surname>Mlinkó</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4257</fpage>
<lpage>4258</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004257">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004257">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>819. The chemistry of gum labdanum. Part I. Some acidic constituents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004259</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>J. D.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
<name><surname>Bowers</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4259</fpage>
<lpage>4262</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004259">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004259">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>820. The chemistry of gum labdanum. Part II. The structure of labdanolic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>J. D.</given-names></name>
<name><surname>Halsall</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4262</fpage>
<lpage>4271</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>821. The formation of nitrosochlorides and nitrosate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004271</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thorne</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4271</fpage>
<lpage>4275</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004271">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004271">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>822. Oxygen heterocycles. Part VI. Orientation in the substitution of 2-methoxydibenzofuran</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004276</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Routier</surname>
<given-names>Cl.</given-names></name>
<name><surname>Buu-Hoï</surname>
<given-names>Ng. Ph.</given-names></name>
<name><surname>Royer</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4276</fpage>
<lpage>4279</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004276">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004276">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>823. Application of the Bruckner method to the synthesis of phenanthridine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004280</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Govindachari</surname>
<given-names>T. R.</given-names></name>
<name><surname>Nagarajan</surname>
<given-names>K.</given-names></name>
<name><surname>Pai</surname>
<given-names>B. R.</given-names></name>
<name><surname>Arumugam</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4280</fpage>
<lpage>4283</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004280">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004280">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>824. Studies in aromatic nucleophilic replacement. Part VI. Some effects of alkyl groups</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004284</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
<name><surname>Fayiga</surname>
<given-names>T. O.</given-names></name>
<name><surname>Hirst</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4284</fpage>
<lpage>4288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004284">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004284">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>825. A theoretical investigation of the chemical reactivity of benziminazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004288</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>R. D.</given-names></name>
<name><surname>Heffernan</surname>
<given-names>M. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4288</fpage>
<lpage>4291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004288">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004288">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>826. Triad prototropic systems. Part IV. The effect of substituents on the mobility of the azomethinecarboxylic acids derived from ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004292</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddar</surname>
<given-names>F. G.</given-names></name>
<name><surname>Sherif</surname>
<given-names>Sayed A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4292</fpage>
<lpage>4295</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004292">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004292">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>827. Fission of esters of carboxylic acids by boron trichloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004296</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Wheelans</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4296</fpage>
<lpage>4300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004296">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004296">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>828. Curvularin. Part I. Isolation and partial characterisation of a metabolic product from a new species of &lt;i&gt;Curvularia&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004301</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4301</fpage>
<lpage>4305</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004301">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004301">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>829. The preparation of some dimeric &lt;i&gt;sec&lt;/i&gt;.-Aminoboron dihalides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004305</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Musgrave</surname>
<given-names>O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4305</fpage>
<lpage>4307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004305">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004305">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>830. The synthesis of 1 : 2 : 7 : 8-tetrahydro-3-methoxy- and 1 : 2 : 7 : 8-tetrahydro-3 : 10-dimethoxy-chrysene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004308</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collins</surname>
<given-names>J. F.</given-names></name>
<name><surname>Smith</surname>
<given-names>Herchel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4308</fpage>
<lpage>4310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>831. Ionophoresis of carbohydrates. Part IV. Separations of carbohydrates on fibreglass sheets</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bourne</surname>
<given-names>E. J.</given-names></name>
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Grant</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4311</fpage>
<lpage>4314</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>832. Electronic spectra of organic molecules and their interpretation. Part II. Effect of terminal halogen atoms of conjugated systems on &lt;i&gt;K&lt;/i&gt;-bands</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004314</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Burawoy</surname>
<given-names>A.</given-names></name>
<name><surname>Thompson</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4314</fpage>
<lpage>4320</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004314">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004314">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>833. Studies in the synthesis of cortisone. Part XIII. The epimeric 3β : 7-dihydroxyergost-22-en-11-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004320</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elks</surname>
<given-names>J.</given-names></name>
<name><surname>Phillipps</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4320</fpage>
<lpage>4325</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004320">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004320">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>834. Studies in the synthesis of cortisone. Part XIV. Acetylhydrazones and azines of steroidal ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004326</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elks</surname>
<given-names>J.</given-names></name>
<name><surname>Phillipps</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4326</fpage>
<lpage>4330</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004326">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004326">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>835. Studies in the synthesis of cortisone. Part XV. Improvements in the conversion of hecogenin into 3β : 12β-diacetoxy-5α : 25&lt;i&gt;D&lt;/i&gt;-spirostan-11-one and a study of the isomeric 11 : 12-ketols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004330</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elks</surname>
<given-names>J.</given-names></name>
<name><surname>Phillipps</surname>
<given-names>G. H.</given-names></name>
<name><surname>Walker</surname>
<given-names>T.</given-names></name>
<name><surname>Wyman</surname>
<given-names>L. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4330</fpage>
<lpage>4344</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004330">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004330">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>836. Studies in the synthesis of cortisone. Part XVI. A new method of preparing 11-oxotigogenin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>J. H.</given-names></name>
<name><surname>Elks</surname>
<given-names>J.</given-names></name>
<name><surname>Phillipps</surname>
<given-names>G. H.</given-names></name>
<name><surname>Wyman</surname>
<given-names>L. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4344</fpage>
<lpage>4350</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>837. Studies in the synthesis of cortisone. Part XVII. The bromination of cholestan-3-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004351</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crowne</surname>
<given-names>C. W. P.</given-names></name>
<name><surname>Evans</surname>
<given-names>R. M.</given-names></name>
<name><surname>Green</surname>
<given-names>G. F. H.</given-names></name>
<name><surname>Long</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4351</fpage>
<lpage>4356</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004351">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004351">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>838. Studies in the synthesis of cortisone. Part XVIII. The preparation of cortisone esters from 4 : 5α-dihydrocortisone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004356</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>R. M.</given-names></name>
<name><surname>Hamlet</surname>
<given-names>J. C.</given-names></name>
<name><surname>Hunt</surname>
<given-names>J. S.</given-names></name>
<name><surname>Jones</surname>
<given-names>P. G.</given-names></name>
<name><surname>Long</surname>
<given-names>A. G.</given-names></name>
<name><surname>Oughton</surname>
<given-names>J. F.</given-names></name>
<name><surname>Stephenson</surname>
<given-names>L.</given-names></name>
<name><surname>Walker</surname>
<given-names>T.</given-names></name>
<name><surname>Wilson</surname>
<given-names>B. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4356</fpage>
<lpage>4368</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004356">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004356">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>839. Barringtogenol and barringtogenic acid, two new triterpenoid sapogenins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004369</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anantaraman</surname>
<given-names>R.</given-names></name>
<name><surname>Pillai</surname>
<given-names>K. S. Madhavan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4369</fpage>
<lpage>4373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004369">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004369">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>840. The identity of the cubic oxide present in films on iron</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. Eurof</given-names></name>
<name><surname>Evans</surname>
<given-names>U. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4373</fpage>
<lpage>4375</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>841. Four-, five-, and six-covalent palladium(II) complexes with a di(tertiary) arsine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004375</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>C. M.</given-names></name>
<name><surname>Nyholm</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4375</fpage>
<lpage>4383</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004375">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004375">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>842. Stereochemistry of &lt;i&gt;cyclo&lt;/i&gt;hexane derivatives. Part IV. Some secondary tertiary 1 : 2-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004384</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jefferies</surname>
<given-names>P. R.</given-names></name>
<name><surname>Milligan</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4384</fpage>
<lpage>4390</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004384">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004384">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>843. Stereochemistry of &lt;i&gt;cyclo&lt;/i&gt;hexane derivatives. Part V. Infrared spectra and conformations of stereoisomeric 1 : 2-diols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004391</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cole</surname>
<given-names>A. R. H.</given-names></name>
<name><surname>Jefferies</surname>
<given-names>P. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4391</fpage>
<lpage>4397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004391">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004391">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>844. The decomposition of arylazotriarylmethanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>G. L.</given-names></name>
<name><surname>Hey</surname>
<given-names>D. H.</given-names></name>
<name><surname>Williams</surname>
<given-names>Gareth H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4397</fpage>
<lpage>4408</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>845. Wessely–Moser rearrangement of chromonols and flavonols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004409</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Donnelly</surname>
<given-names>(Miss) D. M.</given-names></name>
<name><surname>Philbin</surname>
<given-names>(Mrs.) E. M.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4409</fpage>
<lpage>4411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004409">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004409">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>846. Thermal cyclization of &lt;i&gt;o&lt;/i&gt;-aroyloxyacetoarones. Part III. Synthesis in the chromone series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>O'Toole</surname>
<given-names>T. M.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4411</fpage>
<lpage>4414</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>847. Studies of sultones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004414</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Philbin</surname>
<given-names>(Mrs.) E. M.</given-names></name>
<name><surname>Stuart</surname>
<given-names>E. R.</given-names></name>
<name><surname>Timoney</surname>
<given-names>R. F.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4414</fpage>
<lpage>4417</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004414">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004414">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>848. Some 5α : 6α-epoxy-3-oxo-steroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004417</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ellis</surname>
<given-names>Bernard</given-names></name>
<name><surname>Petrow</surname>
<given-names>Vladimir</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4417</fpage>
<lpage>4419</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004417">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004417">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>849. Syntheses in the quinazolone series. Part IV. The conversion of &lt;i&gt;N&lt;/i&gt;-aroylorthanilamides into 2-arylquinazol-4-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
<name><surname>Wadge</surname>
<given-names>(the late) George</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4420</fpage>
<lpage>4421</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>850. Bisdiguanides having antibacterial activity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004422</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rose</surname>
<given-names>F. L.</given-names></name>
<name><surname>Swain</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4422</fpage>
<lpage>4425</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004422">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004422">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>851. The synthesis of α- and β-phenyladipic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004426</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>K.</given-names></name>
<name><surname>Ellis</surname>
<given-names>G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4426</fpage>
<lpage>4428</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004426">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004426">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>852. The reduction of carbon monoxide by lithium aluminium hydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>J. F.</given-names></name>
<name><surname>Neale</surname>
<given-names>A. J.</given-names></name>
<name><surname>Turner</surname>
<given-names>H. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4428</fpage>
<lpage>4433</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>853. Polyazanaphthalenes. Part IV. Further derivatives of 1 : 3 : 5- and 1 : 3 : 8-triazanaphthalene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004433</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oakes</surname>
<given-names>V.</given-names></name>
<name><surname>Rydon</surname>
<given-names>H. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4433</fpage>
<lpage>4438</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004433">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004433">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>854. Structural chemistry of the alkoxides. Part VIII. Isomeric butoxides and pentyloxides of niobium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004439</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Chakravarti</surname>
<given-names>B. N.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4439</fpage>
<lpage>4442</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004439">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004439">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>855. The chemical action of ultrasonic waves</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004442</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Parke</surname>
<given-names>A. V. M.</given-names></name>
<name><surname>Taylor</surname>
<given-names>Duncan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4442</fpage>
<lpage>4450</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004442">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004442">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>856. Curare and related topics. Part II. The structure and anomalous optical rotation of &lt;i&gt;iso&lt;/i&gt;chondrodendrine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004451</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jeffreys</surname>
<given-names>John A. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4451</fpage>
<lpage>4455</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004451">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004451">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>857. Wessely–Moser rearrangement with xanthones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004455</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Philbin</surname>
<given-names>(Mrs.) E. M.</given-names></name>
<name><surname>Swirski</surname>
<given-names>J.</given-names></name>
<name><surname>Wheeler</surname>
<given-names>T. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4455</fpage>
<lpage>4458</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004455">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004455">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>858. Acyl &lt;i&gt;iso&lt;/i&gt;thiocyanates. Part I. The synthesis of esters of &lt;i&gt;N&lt;/i&gt;-acyldithiocarbamic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004458</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Elmore</surname>
<given-names>D. T.</given-names></name>
<name><surname>Ogle</surname>
<given-names>J. R.</given-names></name>
<name><surname>Fletcher</surname>
<given-names>(Mrs.) W.</given-names></name>
<name><surname>Toseland</surname>
<given-names>P. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4458</fpage>
<lpage>4463</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004458">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004458">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>859. The electrical conductances of solutions in nitric acid. Part I. Solutions of dinitrogen pentoxide, and of water. The extent of the self-dissociation of nitric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lee</surname>
<given-names>W. H.</given-names></name>
<name><surname>Millen</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4463</fpage>
<lpage>4469</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>860. The chemistry of extractives from hardwoods. Part XXVII. The structure of terminolic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004469</article-id><contrib-group><contrib contrib-type="author">
<name><surname>King</surname>
<given-names>F. E.</given-names></name>
<name><surname>King</surname>
<given-names>T. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4469</fpage>
<lpage>4477</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004469">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004469">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>861. The chemistry of extractives from hardwoods. Part XXVIII. The occurrence of 3 : 4 : 3′ : 5′-tetrahydroxy- and 3 : 4 : 5 : 3′ : 5′-pentahydroxy-stilbene in &lt;i&gt;Vouacapoua&lt;/i&gt; species</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004477</article-id><contrib-group><contrib contrib-type="author">
<name><surname>King</surname>
<given-names>F. E.</given-names></name>
<name><surname>King</surname>
<given-names>T. J.</given-names></name>
<name><surname>Godson</surname>
<given-names>D. H.</given-names></name>
<name><surname>Manning</surname>
<given-names>L. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4477</fpage>
<lpage>4480</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004477">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004477">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>862. The simple fluorides of iridium, including the new trifluoride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004481</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robinson</surname>
<given-names>P. L.</given-names></name>
<name><surname>Westland</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4481</fpage>
<lpage>4487</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004481">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004481">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>863. The composition of &lt;i&gt;Hakea acicularis&lt;/i&gt; gum</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004487</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Stephen</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4487</fpage>
<lpage>4490</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004487">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004487">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>864. 4 : 4-Dimethylsteroids. Part II. Some androstane and pregnane derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004490</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Adams</surname>
<given-names>(Mrs.) W. J.</given-names></name>
<name><surname>Patel</surname>
<given-names>D. K.</given-names></name>
<name><surname>Petrow</surname>
<given-names>V.</given-names></name>
<name><surname>Stuart-Webb</surname>
<given-names>(Mrs.) I. A.</given-names></name>
<name><surname>Sturgeon</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4490</fpage>
<lpage>4495</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004490">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004490">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>865. Infrared spectra of metal ammines and related compounds. Part II. The &lt;i&gt;trans&lt;/i&gt;-effect in platinous complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004495</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Powell</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4495</fpage>
<lpage>4498</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004495">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004495">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>866. Molecular polarisation in ternary systems comprising benzene, pyridine, and an alcohol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004499</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cleverdon</surname>
<given-names>D.</given-names></name>
<name><surname>Collins</surname>
<given-names>G. B.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4499</fpage>
<lpage>4507</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004499">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004499">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>867. Dielectric polarisation studies of the formation of hydrogen-bond complexes by alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boud</surname>
<given-names>(the late) A. H.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4507</fpage>
<lpage>4513</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>868. The structure of molecules and ions of the type X&lt;sub&gt;2&lt;/sub&gt;A·AX&lt;sub&gt;2&lt;/sub&gt;, X&lt;sub&gt;2&lt;/sub&gt;A·AY&lt;sub&gt;2&lt;/sub&gt;, and YXA·AXY</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004514</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wheatley</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4514</fpage>
<lpage>4517</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004514">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004514">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>869. Reduced cyclic compounds. Part II. The synthesis of 1-1′-acetoxyvinyl&lt;i&gt;cyclo&lt;/i&gt;hexene and its reactions with some dienophils</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004518</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>M. F.</given-names></name>
<name><surname>Brooks</surname>
<given-names>G. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4518</fpage>
<lpage>4524</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004518">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004518">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>870. Thiadiazoles. Part IV. The oxidation of &lt;i&gt;N&lt;/i&gt;-(aroylamidino)thioureas</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kurzer</surname>
<given-names>Frederick</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4524</fpage>
<lpage>4531</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>871. Amino-sugars and related compounds. Part I. The deamination of D-glucosamine hydrochloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004531</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bera</surname>
<given-names>B. C.</given-names></name>
<name><surname>Foster</surname>
<given-names>A. B.</given-names></name>
<name><surname>Stacey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4531</fpage>
<lpage>4535</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004531">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004531">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>872. Synthetical experiments in the chelidonine–sanguinarine group of the alkaloids. Part IV</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004535</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bailey</surname>
<given-names>A. S.</given-names></name>
<name><surname>Worthing</surname>
<given-names>C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4535</fpage>
<lpage>4543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004535">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004535">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>873. The chemical synthesis of polysaccharides. Part I. Synthesis of gentiodextrins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004543</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haq</surname>
<given-names>S.</given-names></name>
<name><surname>Whelan</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4543</fpage>
<lpage>4549</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004543">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004543">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>874. The chemistry of santonin. Part III. The stereochemistry of some reduction products of santonin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004549</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cocker</surname>
<given-names>Wesley</given-names></name>
<name><surname>McMurry</surname>
<given-names>T. B. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4549</fpage>
<lpage>4557</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004549">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004549">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>875. The reaction between aromatic compounds and derivatives of tertiary acids. Part VIII. The use of an infrared gas analyser for the quantitative determination of carbon monoxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004558</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grundy</surname>
<given-names>Michael E.</given-names></name>
<name><surname>Rothstein</surname>
<given-names>Eugene</given-names></name>
<name><surname>Hsü</surname>
<given-names>Wei-Hwa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4558</fpage>
<lpage>4561</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004558">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004558">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>876. The reaction between aromatic compounds and derivatives of tertiary acids. Part IX. Concentration and environmental factors influencing the elimination of carbon monoxide from pivaloyl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004561</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grundy</surname>
<given-names>Michael E.</given-names></name>
<name><surname>Rothstein</surname>
<given-names>Eugene</given-names></name>
<name><surname>Hsü</surname>
<given-names>Wei-Hwa</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4561</fpage>
<lpage>4571</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004561">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004561">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>877. The thermodynamics of the formation of complex ions of ethylenediaminetetra-acetic acid and bivalent cations</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004571</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Care</surname>
<given-names>R. A.</given-names></name>
<name><surname>Staveley</surname>
<given-names>L. A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4571</fpage>
<lpage>4579</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004571">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004571">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>878. The sulphates and selenate of polonium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004579</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bagnall</surname>
<given-names>K. W.</given-names></name>
<name><surname>Freeman</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4579</fpage>
<lpage>4582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>879. Cytidine diphosphate ribitol from &lt;i&gt;Lactobacillus arabinosus&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004583</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddiley</surname>
<given-names>J.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Carss</surname>
<given-names>B.</given-names></name>
<name><surname>Mathias</surname>
<given-names>A. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4583</fpage>
<lpage>4588</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004583">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004583">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>880. Tryptamines, carbolines, and related compounds. Part II. A convenient synthesis of tryptamines and β-carbolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004589</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Shapiro</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4589</fpage>
<lpage>4592</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004589">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004589">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>881. Tryptamines, carbolines, and related compounds. Part III. 1-Methyl- and 1 : &lt;i&gt;N&lt;/i&gt;-dimethyl-tryptamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004593</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4593</fpage>
<lpage>4602</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004593">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004593">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>882. Some cholesteryl phosphates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004603</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Montgomery</surname>
<given-names>H. A. C.</given-names></name>
<name><surname>Turnbull</surname>
<given-names>J. H.</given-names></name>
<name><surname>Wilson</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4603</fpage>
<lpage>4606</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004603">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004603">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>883. Phosphonic polymers. Part I. The copolymerisation of diethyl vinylphosphonate and styrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004607</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arcus</surname>
<given-names>C. L.</given-names></name>
<name><surname>Matthews</surname>
<given-names>R. J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4607</fpage>
<lpage>4612</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004607">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004607">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>884. The reaction between phosphorus trichloride and bromine. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004613</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>G. S.</given-names></name>
<name><surname>Payne</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4613</fpage>
<lpage>4616</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004613">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004613">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>885. Non-aqueous solutions of phosphorus pentabromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004617</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>G. S.</given-names></name>
<name><surname>Payne</surname>
<given-names>D. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4617</fpage>
<lpage>4621</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004617">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004617">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>886. Pteridine studies. Part X. Pteridines with more than one hydroxy- or amino-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004621</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Lister</surname>
<given-names>J. H.</given-names></name>
<name><surname>Pedersen</surname>
<given-names>Christian</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4621</fpage>
<lpage>4628</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004621">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004621">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>887. Synthesis of polycyclic compounds. Part VI. The preparation of 1 : 2 : 3 : 4-tetrahydro-6-methoxy-1-oxo-4-&lt;i&gt;iso&lt;/i&gt;propylnaphthalene and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004629</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bardhan</surname>
<given-names>J. C.</given-names></name>
<name><surname>Mukherji</surname>
<given-names>D. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4629</fpage>
<lpage>4633</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004629">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004629">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>888. Border-line mechanisms in nucleophilic displacement reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004633</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4633</fpage>
<lpage>4637</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004633">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004633">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>889. The relation between configuration and conjugation in diphenyl derivatives. Part VII. Halogenodiphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004637</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaven</surname>
<given-names>G. H.</given-names></name>
<name><surname>Hall</surname>
<given-names>D. Muriel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4637</fpage>
<lpage>4646</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004637">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004637">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>890. Friedel–Crafts acylation and alkylation. A comparison of inter- and intra-molecular processes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004647</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddeley</surname>
<given-names>G.</given-names></name>
<name><surname>Williamson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4647</fpage>
<lpage>4653</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004647">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004647">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>891. The reaction of tetra-alkylammonium halides with potassium in liquid ammonia</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004653</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hazlehurst</surname>
<given-names>D. A.</given-names></name>
<name><surname>Holliday</surname>
<given-names>A. K.</given-names></name>
<name><surname>Pass</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4653</fpage>
<lpage>4658</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004653">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004653">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>892. Synthesis of “6-succinoaminopurine”[6-(1 : 2-dicarboxyethyl-amino)purine]</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004659</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddiley</surname>
<given-names>J.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Hawker</surname>
<given-names>F. J.</given-names></name>
<name><surname>Stephenson</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4659</fpage>
<lpage>4661</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004659">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004659">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>893. Tetronic acids and related compounds. Part II. The synthesis of (±)-carolinic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004661</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
<name><surname>Plimmer</surname>
<given-names>J. R.</given-names></name>
<name><surname>Stanners</surname>
<given-names>A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4661</fpage>
<lpage>4664</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004661">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004661">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004665</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haynes</surname>
<given-names>L. J.</given-names></name>
<name><surname>Plimmer</surname>
<given-names>J. R.</given-names></name>
<name><surname>Lippner</surname>
<given-names>M. P.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>Muriel L.</given-names></name>
<name><surname>Lowenstein</surname>
<given-names>J. M.</given-names></name>
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Feld</surname>
<given-names>R.</given-names></name>
<name><surname>Kennedy</surname>
<given-names>J.</given-names></name>
<name><surname>Lane</surname>
<given-names>E. S.</given-names></name>
<name><surname>Willans</surname>
<given-names>J. L.</given-names></name>
<name><surname>Cavalla</surname>
<given-names>J. F.</given-names></name>
<name><surname>Braude</surname>
<given-names>(the late) E. A.</given-names></name>
<name><surname>Erskine</surname>
<given-names>R. L.</given-names></name>
<name><surname>Petrow</surname>
<given-names>Vladimir</given-names></name>
<name><surname>Stuart-Webb</surname>
<given-names>(Mrs.) Isobel A.</given-names></name>
<name><surname>Hawke</surname>
<given-names>J. G.</given-names></name>
<name><surname>Stimson</surname>
<given-names>V. R.</given-names></name>
<name><surname>Gladych</surname>
<given-names>J. M. Z.</given-names></name>
<name><surname>Taylor</surname>
<given-names>E. P.</given-names></name>
<name><surname>Meakins</surname>
<given-names>G. D.</given-names></name>
<name><surname>Rodig</surname>
<given-names>O. R.</given-names></name>
<name><surname>O'Donnell</surname>
<given-names>T. A.</given-names></name>
<name><surname>Banks</surname>
<given-names>R. E.</given-names></name>
<name><surname>Musgrave</surname>
<given-names>W. K. R.</given-names></name>
<name><surname>Albert</surname>
<given-names>Adrien</given-names></name>
<name><surname>Pedersen</surname>
<given-names>Christian</given-names></name>
<name><surname>Barakat</surname>
<given-names>M. Z.</given-names></name>
<name><surname>Abdel-Wahab</surname>
<given-names>M. F.</given-names></name>
<name><surname>El-Sadr</surname>
<given-names>M. M.</given-names></name>
<name><surname>Batten</surname>
<given-names>J. J.</given-names></name>
<name><surname>Sewell</surname>
<given-names>O. K.</given-names></name>
<name><surname>Turnbull</surname>
<given-names>J. H.</given-names></name></contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4665</fpage>
<lpage>4700</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004665">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004665">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>918. Co-ordination compounds between ethylenediaminetetra-acetic acid and gallium, indium, and thallium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004701</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Saito</surname>
<given-names>Kazuo</given-names></name>
<name><surname>Terrey</surname>
<given-names>(the late) Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4701</fpage>
<lpage>4704</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004701">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004701">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>919. Observations on ammonium ferric disulphate dodecahydrate (ammonium ferric alum) and some of its derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004705</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bassett</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4705</fpage>
<lpage>4708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004705">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004705">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>920. A new synthesis of 2 : 3 : 5 : 6-substituted 4-pyrimidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004708</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Staskun</surname>
<given-names>Benjamin</given-names></name>
<name><surname>Stephen</surname>
<given-names>Henry</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4708</fpage>
<lpage>4710</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004708">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004708">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>921. Structure and reactivity of the oxy-anions of transition metals. Part II. Investigations by electron-spin resonance</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004710</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carrington</surname>
<given-names>A.</given-names></name>
<name><surname>Ingram</surname>
<given-names>D. J. E.</given-names></name>
<name><surname>Schonland</surname>
<given-names>D.</given-names></name>
<name><surname>Symons</surname>
<given-names>M. C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4710</fpage>
<lpage>4715</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004710">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004710">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>922. Picrotoxin and tutin. Part VIII</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004715</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johns</surname>
<given-names>R. B.</given-names></name>
<name><surname>Slater</surname>
<given-names>S. N.</given-names></name>
<name><surname>Woods</surname>
<given-names>R. J.</given-names></name>
<name><surname>Brasch</surname>
<given-names>D.</given-names></name>
<name><surname>Gee</surname>
<given-names>Roy</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4715</fpage>
<lpage>4727</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004715">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004715">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>923. Two hypothetical metabolites of proquanil (“paludrine”)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004727</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
<name><surname>Taylor</surname>
<given-names>N. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4727</fpage>
<lpage>4731</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004727">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004727">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>924. Several quinoxalines of biological interest</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004731</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Acheson</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4731</fpage>
<lpage>4735</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004731">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004731">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>925. Kinetics of the decarboxylation of oxaloacetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004736</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gelles</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4736</fpage>
<lpage>4739</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004736">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004736">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>926. By-ways of synthesis of cortisone from hecogenin. Part I. 9 : 11-Dehydrohecogenin as intermediate in preparation of 11-oxygenated compounds (11-oxotigogenin and 3β-acetoxy-17α-hydroxyallo-pregnane-11 : 20-dione)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Callow</surname>
<given-names>R. K.</given-names></name>
<name><surname>James</surname>
<given-names>V. H. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4739</fpage>
<lpage>4743</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004739">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>927. By-ways of synthesis of cortisone from hecogenin. Part II. A route to 11-oxygenated compounds through 3β : 20β-diacetoxy-11-bromoallopregnan-12-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004744</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Callow</surname>
<given-names>R. K.</given-names></name>
<name><surname>James</surname>
<given-names>V. H. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4744</fpage>
<lpage>4749</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004744">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004744">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>928. The structure and stereochemistry of tazettine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004749</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ikeda</surname>
<given-names>T.</given-names></name>
<name><surname>Taylor</surname>
<given-names>W. I.</given-names></name>
<name><surname>Tsuda</surname>
<given-names>Y.</given-names></name>
<name><surname>Uyeo</surname>
<given-names>S.</given-names></name>
<name><surname>Yajima</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4749</fpage>
<lpage>4761</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004749">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004749">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>929. Researches on acetylenic compounds. Part LIII. The relative strengths of some unsaturated carboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004761</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mansfield</surname>
<given-names>G. H.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4761</fpage>
<lpage>4764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004761">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004761">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>930. Researches on acetylenic compounds. Part LIV. The preparation and synthetical applications of ethynylmagnesium bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004765</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jones</surname>
<given-names>E. R. H.</given-names></name>
<name><surname>Skatteböl</surname>
<given-names>L.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4765</fpage>
<lpage>4768</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004765">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004765">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>931. The polycondensation of benzyl chloride catalysed by stannic chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004768</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Valentine</surname>
<given-names>L.</given-names></name>
<name><surname>Winter</surname>
<given-names>R. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4768</fpage>
<lpage>4779</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004768">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004768">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>932. The polarography of some simple pyrazine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004780</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wiggins</surname>
<given-names>L. F.</given-names></name>
<name><surname>Wise</surname>
<given-names>W. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4780</fpage>
<lpage>4782</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004780">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004780">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>933. Experiments on the preparation of indolocarbazoles. Part IX. The preparation of 9-methylindolo(2′ : 3′-1 : 2)carbazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004783</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brunton</surname>
<given-names>R. J.</given-names></name>
<name><surname>Drayson</surname>
<given-names>F. K.</given-names></name>
<name><surname>Plant</surname>
<given-names>(the late) S. G. P.</given-names></name>
<name><surname>Tomlinson</surname>
<given-names>Muriel L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4783</fpage>
<lpage>4785</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004783">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004783">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>934. Reactions of organic peroxides. Part VIII. 1 : 3 : 3-Trimethylindan-1-yl hydroperoxide and its conversion into 2 : 4 : 4-trimethylchroman derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004785</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Webster</surname>
<given-names>William</given-names></name>
<name><surname>Young</surname>
<given-names>Donald P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4785</fpage>
<lpage>4791</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004785">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004785">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>935. Derivatives of thionaphthen. Part II. Thionaphthen derivatives formed by cyclisation of acetonyl aryl sulphides and aryl phenacyl sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004791</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banfield</surname>
<given-names>J. E.</given-names></name>
<name><surname>Davies</surname>
<given-names>W.</given-names></name>
<name><surname>Gamble</surname>
<given-names>N. W.</given-names></name>
<name><surname>Middleton</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4791</fpage>
<lpage>4799</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004791">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004791">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>936. Quantitative microestimation of formaldehyde in the presence of periodate and its application to the structural examination of carbohydrate phenylosazones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004799</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hough</surname>
<given-names>L.</given-names></name>
<name><surname>Powell</surname>
<given-names>D. B.</given-names></name>
<name><surname>Woods</surname>
<given-names>B. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4799</fpage>
<lpage>4803</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004799">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004799">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>937. Aryldihydroresorcinols. Part II. The influence of the nitro-group in dihydro-5-&lt;i&gt;o&lt;/i&gt;-nitrostyrylresorcinol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004803</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ayling</surname>
<given-names>E. E.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4803</fpage>
<lpage>4806</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004803">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004803">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>938. The degradation of xylobiose and xylotriose by alkali</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004807</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aspinall</surname>
<given-names>G. O.</given-names></name>
<name><surname>Carter</surname>
<given-names>(Miss) Mary E.</given-names></name>
<name><surname>Los</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4807</fpage>
<lpage>4810</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004807">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004807">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>939. The infrared absorption spectra of the carbonyl group in methoxy-anthraquinones, and in the hydrochlorides of 1-methoxyanthraquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004811</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wiles</surname>
<given-names>L. A.</given-names></name>
<name><surname>Thomas</surname>
<given-names>L. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4811</fpage>
<lpage>4814</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004811">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004811">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>940. The formation of osazones during attempted fischer indole syntheses</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004814</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kinsley</surname>
<given-names>D. A.</given-names></name>
<name><surname>Plant</surname>
<given-names>(the late) S. G. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4814</fpage>
<lpage>4817</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004814">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004814">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>941. Steroids and walden inversion. Part XXXIV. Solvolysis of cholesteryl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonate with thiophenoxide ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004817</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shoppee</surname>
<given-names>C. W.</given-names></name>
<name><surname>Richards</surname>
<given-names>H. C.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4817</fpage>
<lpage>4821</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004817">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004817">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>942. Steroids and walden inversion. Part XXXV. &lt;i&gt;NN&lt;/i&gt;-dimethylcholest-7-en-3α- and -3β-ylamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004821</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Evans</surname>
<given-names>D. E.</given-names></name>
<name><surname>Summers</surname>
<given-names>G. H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4821</fpage>
<lpage>4824</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004821">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004821">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>943. Urinary steroids and related compounds. Part I. 11-Substituted derivatives of androsterone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004825</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Klyne</surname>
<given-names>W.</given-names></name>
<name><surname>Ridley</surname>
<given-names>Sheila</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4825</fpage>
<lpage>4828</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004825">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004825">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>944. Adsorption from binary liquid mixtures on activated alumina</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004828</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kipling</surname>
<given-names>J. J.</given-names></name>
<name><surname>Peakall</surname>
<given-names>D. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4828</fpage>
<lpage>4840</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004828">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004828">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>945. Crystal symmetry, and the adsorption of dyes by growing crystals. Part I. Ammonium nitrate IV</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004841</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Whetstone</surname>
<given-names>John</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4841</fpage>
<lpage>4847</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004841">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004841">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>946. A polarographic study of copper malonate complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004847</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gelles</surname>
<given-names>E.</given-names></name>
<name><surname>Nancollas</surname>
<given-names>G. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4847</fpage>
<lpage>4850</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004847">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004847">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>947. Quassin and &lt;i&gt;neo&lt;/i&gt;quassin. Part V</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004850</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beer</surname>
<given-names>R. J. S.</given-names></name>
<name><surname>Dutton</surname>
<given-names>B. G.</given-names></name>
<name><surname>Jaquiss</surname>
<given-names>D. B.</given-names></name>
<name><surname>Robertson</surname>
<given-names>Alexander</given-names></name>
<name><surname>Savige</surname>
<given-names>W. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4850</fpage>
<lpage>4855</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004850">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004850">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>948. The structure of molecular compounds. Part XI. Crystal structure of the addition complex of quinol and methyl cyanide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004855</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wallwork</surname>
<given-names>S. C.</given-names></name>
<name><surname>Powell</surname>
<given-names>H. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4855</fpage>
<lpage>4858</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004855">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004855">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>949. Aromatic reactivity. Part I. Effects of substituents on the acid cleavage of phenyltrimethylsilanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004858</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4858</fpage>
<lpage>4864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004858">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004858">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>950. Phosphorescence and fluorescence of some aromatic nitro-amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004865</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Foster</surname>
<given-names>R.</given-names></name>
<name><surname>Hammick</surname>
<given-names>D. Ll.</given-names></name>
<name><surname>Hood</surname>
<given-names>G. M.</given-names></name>
<name><surname>Sanders</surname>
<given-names>A. C. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4865</fpage>
<lpage>4868</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004865">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004865">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>951. Infrared spectra of natural products. Part VI. The characterization of equatorial and axial 3-hydroxyl groups in triterpenoids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004868</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allsop</surname>
<given-names>(Miss) I. L.</given-names></name>
<name><surname>Cole</surname>
<given-names>A. R. H.</given-names></name>
<name><surname>White</surname>
<given-names>D. E.</given-names></name>
<name><surname>Willix</surname>
<given-names>R. L. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4868</fpage>
<lpage>4873</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004868">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004868">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>952. Nucleotides. Part XXXIX. 5′-Deoxy-5′-iodo-&lt;i&gt;O&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt; : 2′-&lt;i&gt;cyclo&lt;/i&gt;uridine : an X-ray crystallographic study</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004873</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>D. M.</given-names></name>
<name><surname>Cochran</surname>
<given-names>W.</given-names></name>
<name><surname>Medlin</surname>
<given-names>E. H.</given-names></name>
<name><surname>Varadarajan</surname>
<given-names>S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4873</fpage>
<lpage>4876</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004873">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004873">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>953. The equilibrium in the system : water–6-hexanolactam (ɛ-caprolactam)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004876</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Meggy</surname>
<given-names>A. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4876</fpage>
<lpage>4885</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004876">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004876">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>954. The crystal and molecular structure of thianthren</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004886</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lynton</surname>
<given-names>H.</given-names></name>
<name><surname>Cox</surname>
<given-names>E. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4886</fpage>
<lpage>4895</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004886">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004886">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>955. &lt;i&gt;d&lt;/i&gt;-Orbital contraction in chemical bonding</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004895</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Craig</surname>
<given-names>D. P.</given-names></name>
<name><surname>Magnusson</surname>
<given-names>E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4895</fpage>
<lpage>4909</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004895">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004895">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>956. Hydroaromatic steroid hormones. Part V. Some D-homo-18 : 19-bisnorsteroids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004909</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Birch</surname>
<given-names>A. J.</given-names></name>
<name><surname>Smith</surname>
<given-names>Herchel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4909</fpage>
<lpage>4916</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004909">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004909">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>957. Germanium esters. Part I. Parachors and molecular structure</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004916</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bradley</surname>
<given-names>D. C.</given-names></name>
<name><surname>Kay</surname>
<given-names>L. J.</given-names></name>
<name><surname>Wardlaw</surname>
<given-names>W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4916</fpage>
<lpage>4926</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004916">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004916">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>958. Radical-capture agents in tetralin. Measurement of relative efficiencies and correlation with structure</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004926</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>D. S.</given-names></name>
<name><surname>Goldsmith</surname>
<given-names>H. L.</given-names></name>
<name><surname>Gupta</surname>
<given-names>A. K.</given-names></name>
<name><surname>Lester</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4926</fpage>
<lpage>4933</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004926">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004926">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>959. Kinetics and mechanism of bromination of phenol with bromine and iodine bromide in glacial acetic acid and carbon tetrachloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004934</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Yeddanapalli</surname>
<given-names>Lourdu M.</given-names></name>
<name><surname>Gnanapragasam</surname>
<given-names>N. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4934</fpage>
<lpage>4943</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004934">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004934">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>960. The interaction of alkylbenzenes with excess of Friedel–Crafts acetylating agent</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004943</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baddeley</surname>
<given-names>G.</given-names></name>
<name><surname>Wrench</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4943</fpage>
<lpage>4945</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004943">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004943">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>961. Water-soluble complexes of niobium (columbium) and tantalum. Part I. Complexes with α-hydroxy-acids and (2-hydroxyethyl)-amines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004946</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fairbrother</surname>
<given-names>Fred</given-names></name>
<name><surname>Taylor</surname>
<given-names>John B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4946</fpage>
<lpage>4954</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004946">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004946">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>962. Search for spectral evidence of expansion of the valency shell of sulphur in aromatic sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004954</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mangini</surname>
<given-names>A.</given-names></name>
<name><surname>Passerini</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4954</fpage>
<lpage>4959</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004954">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004954">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>963. Energy levels and absorption of some monosubstituted benzene derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004960</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mangini</surname>
<given-names>A.</given-names></name>
<name><surname>Zauli</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4960</fpage>
<lpage>4967</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004960">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004960">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>964. Coenzyme A. Part X. Model experiments on the synthesis of pyrophosphates of &lt;i&gt;N&lt;/i&gt;-pantoylamines. New methods for the debenzylation of esters of pyrophosphoric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004968</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arris</surname>
<given-names>J.</given-names></name>
<name><surname>Baddiley</surname>
<given-names>J.</given-names></name>
<name><surname>Buchanan</surname>
<given-names>J. G.</given-names></name>
<name><surname>Thain</surname>
<given-names>E. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4968</fpage>
<lpage>4973</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004968">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004968">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>965. A molecular rearrangement during the reduction of thionaphthenopyrazole dioxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004974</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barry</surname>
<given-names>W. J.</given-names></name>
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
<name><surname>Simmonds</surname>
<given-names>Alma B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4974</fpage>
<lpage>4978</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004974">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004974">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Notes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004978</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chakrabarti</surname>
<given-names>J. K.</given-names></name>
<name><surname>Dutt</surname>
<given-names>P.</given-names></name>
<name><surname>Dutta</surname>
<given-names>P. C.</given-names></name>
<name><surname>Logan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Newbold</surname>
<given-names>G. T.</given-names></name>
<name><surname>Griffith</surname>
<given-names>J. S.</given-names></name>
<name><surname>Orgel</surname>
<given-names>L. E.</given-names></name>
<name><surname>Chan</surname>
<given-names>W. R.</given-names></name>
<name><surname>Hassall</surname>
<given-names>C. H.</given-names></name>
<name><surname>Ford</surname>
<given-names>M. C.</given-names></name>
<name><surname>Mackay</surname>
<given-names>Donald</given-names></name>
<name><surname>Gerrard</surname>
<given-names>W.</given-names></name>
<name><surname>Lappert</surname>
<given-names>M. F.</given-names></name>
<name><surname>Silver</surname>
<given-names>H. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4978</fpage>
<lpage>4988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004978">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004978">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>International atomic weights, 1955</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004989</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4989</fpage>
<lpage>4989</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004989">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004989">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Editorial report on nomenclature, 1956</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004990</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4990</fpage>
<lpage>4993</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004990">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004990">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</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, 1956</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560004994</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>4994</fpage>
<lpage>5016</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560004994">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560004994">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</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, 1956</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR9560005017</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>5017</fpage>
<lpage>5040</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR9560005017">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR9560005017">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society (Resumed)</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Errata</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/JR956000X001</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>1956</year></pub-date>
<volume>1956</volume>
<issue />
<fpage>X001</fpage>
<lpage>X003</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=JR956000X001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1956/JR/JR956000X001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
</articles>
