{"product_id":"pyridine-and-its-derivatives-volume-14-part-4-hardback-9780470380161","title":"Pyridine and Its Derivatives, Volume 14, Part 4 (Hardback) 9780470380161","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003ePyridine and Its Derivatives, Volume 14, Part 4\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"4\"\u003eErwin Klingsberg (Edited by), E Klingsberg (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470380161, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 1 January 1964\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e724 pages\u003cbr\u003e23.8 x 16.2 x 5 cm, 1.134 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003e\u003cp\u003e\u003ci\u003eThe Chemistry of Heterocyclic Compounds\u003c\/i\u003e, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects – properties, synthesis, reactions, physiological and industrial significance – of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors are recognized authorities, the Chemistry of Heterocyclic Chemistry is considered worldwide as the indispensable resource for organic, bioorganic, and medicinal chemists.\u003c\/p\u003e\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003e\u003cb\u003eXIII. Pyridine Alcohols 1\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eEllis V. \u003c\/i\u003e\u003ci\u003eBrown\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Preparation 2\u003c\/p\u003e \u003cp\u003eB. Properties 10\u003c\/p\u003e \u003cp\u003eC. Reactions 10\u003c\/p\u003e \u003cp\u003eD. Dihydric and Polyhydric Alcohols Containing One Pyridine Nucleus 14\u003c\/p\u003e \u003cp\u003eE. Dihydric AlcoholsContaining TwoPryridineNuclei 16\u003c\/p\u003e \u003cp\u003eF. Side-Chain Hydroxyacid Derivatives 17\u003c\/p\u003e \u003cp\u003eG. Derivatives Containing Both Nuclear and Side-Chain Hydroxyl 18\u003c\/p\u003e \u003cp\u003eH. Tables 27\u003c\/p\u003e \u003cp\u003eI. Bibliography 106\u003c\/p\u003e \u003cp\u003e\u003cb\u003eXIV. Pyridine Aldehydes and Ketones \u003c\/b\u003e\u003cb\u003e123\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eRenat H. Mizzoni\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Pyridine Aldehydes 125\u003c\/p\u003e \u003cp\u003eB. Pyridine Ketones 141\u003c\/p\u003e \u003cp\u003eC. Tables 175\u003c\/p\u003e \u003cp\u003eD. Bibliography 333\u003c\/p\u003e \u003cp\u003e\u003cb\u003eXV. Sulfur and Selenium Compounds of Pytidine 345\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eHarry L. Yale\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Pyridinethiols and Pyridinethiones 347\u003c\/p\u003e \u003cp\u003eB. Pyridylalkythiols 356\u003c\/p\u003e \u003cp\u003eC\u003ci\u003e. \u003c\/i\u003ePyridyl Thioketones 358\u003c\/p\u003e \u003cp\u003eD. Pyridyl Sulfides 358\u003c\/p\u003e \u003cp\u003eE. Pyridylalkyl Sulfides 362\u003c\/p\u003e \u003cp\u003eF. Pyridyl Disulfides 363\u003c\/p\u003e \u003cp\u003eG. Pyridyl Sulfoxides 364\u003c\/p\u003e \u003cp\u003eH. Pyridyl Sulfones 364\u003c\/p\u003e \u003cp\u003eI. Pyridylalkyl Sulfones 366\u003c\/p\u003e \u003cp\u003eJ. Pyridinesulfinic Acids 366\u003c\/p\u003e \u003cp\u003eK. Pyridinesulfonic Acids 367\u003c\/p\u003e \u003cp\u003eL. Pyridyldithiocarbamic Acid and PyridylalkyldithiocarboxylAcid Derivatives 376\u003c\/p\u003e \u003cp\u003eM. Thiocyanatopyridines 377\u003c\/p\u003e \u003cp\u003eN. Biological Activity of Sulfur Compounds of Pyridine 378\u003c\/p\u003e \u003cp\u003e0. Selenium Compounds of Pyridine 380\u003c\/p\u003e \u003cp\u003eP. Tables 382\u003c\/p\u003e \u003cp\u003eQ Bibliography 427\u003c\/p\u003e \u003cp\u003e\u003cb\u003eXVI. Arsenic, Antimony, and Phosphorus Compounds of Pyridine \u003c\/b\u003e\u003cb\u003e439\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eHarry L\u003c\/i\u003e\u003ci\u003e. Yale\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Arsenic Compounds 439\u003c\/p\u003e \u003cp\u003eB. Antimony Compounds 451\u003c\/p\u003e \u003cp\u003eC. Phosphorus Compounds 452\u003c\/p\u003e \u003cp\u003eD. Tables 454\u003c\/p\u003e \u003cp\u003eE. Bibliography 463\u003c\/p\u003e \u003cp\u003eCumulative Author Index 467\u003c\/p\u003e \u003cp\u003eCumulative Subject Index 625\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-Interscience","offers":[{"title":"Brand New","offer_id":52276213088536,"sku":"9780470380161","price":431.37,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470380161.jpg?v=1781365233","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/pyridine-and-its-derivatives-volume-14-part-4-hardback-9780470380161","provider":"Freshly Printed Books","version":"1.0","type":"link"}