{"product_id":"imidazole-and-its-derivatives-volume-6-part-1-hardback-9780470376539","title":"Imidazole and Its Derivatives, Volume 6, Part 1 (Hardback) 9780470376539","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eImidazole and Its Derivatives, Volume 6, Part 1\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\"\u003eKlaus Hofmann (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470376539, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 27 June 2007\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e468 pages\u003cbr\u003e23.8 x 16.4 x 3.6 cm, 0.907 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 \u003ci\u003eChemistry of Heterocyclic Chemistry\u003c\/i\u003e 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\u003ePreface ix\u003c\/p\u003e \u003cp\u003e\u003cb\u003eSection I Chemistry of Classes and Derivatives\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eI. General Properties and Structure of the Imidazoles 3\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Nomenclature 3\u003c\/p\u003e \u003cp\u003eB. Physical Properties 5\u003c\/p\u003e \u003cp\u003eC. Chemical Properties 13\u003c\/p\u003e \u003cp\u003eD. Structural Considerations 17\u003c\/p\u003e \u003cp\u003eE. Tautomeric Character 26\u003c\/p\u003e \u003cp\u003e\u003cb\u003eII. The Alkyl- and Arylimidazoles 33\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Synthetic Procedures 33\u003c\/p\u003e \u003cp\u003eB. Properties and Chemical Behavior 45\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIII. The Oxo- and Hydroxyimidazoles and Their Sulfur Analogues 55\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. The Oxoimidazoles 55\u003c\/p\u003e \u003cp\u003eB. The Hydroxyalkylimidazoles 99\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIV. The Halogenoimidazoles 111\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Bromoimidazoles 111\u003c\/p\u003e \u003cp\u003eB. Chloroimidazoles 119\u003c\/p\u003e \u003cp\u003eC. Chloroalky limidazoles 121\u003c\/p\u003e \u003cp\u003e\u003cb\u003eV. The Nitro-, Arylazo-, and Aminoimidazoles 127\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Nitroimidazoles 127\u003c\/p\u003e \u003cp\u003eB. Arylazoimidazolcs 136\u003c\/p\u003e \u003cp\u003eC. Aminoimidazoles 141\u003c\/p\u003e \u003cp\u003eD. Histamine 143\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVI. The Imidazolecarboxylic and Sulfonic Acids 175\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Imidazolecarhoxylic Acids 175\u003c\/p\u003e \u003cp\u003eB. Imidazolesulfonic Acids 206\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVII. The Imidazolines, 2-Imidazolidones, 2-Imidazolidinethiones, 2-Iminoimidazolidines, and Imidazolidines 213\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Nomenclature 213\u003c\/p\u003e \u003cp\u003eB. 2-ImidazoIines 213\u003c\/p\u003e \u003cp\u003eC. 2-Imidazolidones 226\u003c\/p\u003e \u003cp\u003eD. 2-Imidazolidinethiones 234\u003c\/p\u003e \u003cp\u003eE. 2-Iminoimidazolidines 238\u003c\/p\u003e \u003cp\u003eF. Imidazolidines 242\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVIII. The Benzimidazoles 247\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA Nomenclature 247\u003c\/p\u003e \u003cp\u003eB General Properties 248\u003c\/p\u003e \u003cp\u003eC. Synthetic Procedures 258\u003c\/p\u003e \u003cp\u003eD. The 1-Acylbenzimidazoles and tire Bamberger Reaction 273\u003c\/p\u003e \u003cp\u003eE. The Alkyl- and Arylbenzimidazoles and 1,3-Dialkyibenzimiduzolium Salts 276\u003c\/p\u003e \u003cp\u003eF. The Oxo- and Hydroxybenzimidazolcs and Their Sulfur Analogues 284\u003c\/p\u003e \u003cp\u003eG The Halogenobenzimidazoles 300\u003c\/p\u003e \u003cp\u003eH The Nitro- and Aminobenzimidazoles 304\u003c\/p\u003e \u003cp\u003eI. The Benzimidazolecarboxylic and Sulfonic Acids 313\u003c\/p\u003e \u003cp\u003e\u003cb\u003eSection 2 Systematic Survey and Bibliography \u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eKey to Abbreviations 320\u003c\/p\u003e \u003cp\u003e\u003cb\u003eI. Imidazoles 327\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Alkyl-and Arylimidazoles 327\u003c\/p\u003e \u003cp\u003eB Alkyl- and Arylimidazolium Salts 330\u003c\/p\u003e \u003cp\u003eC. Oxo- and Hydroxyimidazolos and Their Sulfur Analogues 330\u003c\/p\u003e \u003cp\u003eD. Halogenoimidazoles 342\u003c\/p\u003e \u003cp\u003eE. Nitroimidazoles 345\u003c\/p\u003e \u003cp\u003eF. Arylazoimidazoles 346\u003c\/p\u003e \u003cp\u003eG. Aminoimidazoles 347\u003c\/p\u003e \u003cp\u003eH. Cyano- and Isocyanatoimidazolcs 351\u003c\/p\u003e \u003cp\u003eI. Tinidazolcearboxylic Acids 352\u003c\/p\u003e \u003cp\u003eJ. Imidnzolcsulftnic and Sulfonic Acids 363\u003c\/p\u003e \u003cp\u003eK. Imidazole Arscnicals 363\u003c\/p\u003e \u003cp\u003eL. Isoimidazolcs 363\u003c\/p\u003e \u003cp\u003eM. Heteroring-Substituted Imidazoles 364\u003c\/p\u003e \u003cp\u003eN Bi- and Bisimidazoles 366\u003c\/p\u003e \u003cp\u003e\u003cb\u003eII. Imidazolines 367\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. 2-Tmidazolines 367\u003c\/p\u003e \u003cp\u003eB. 3-Imidazolines 372\u003c\/p\u003e \u003cp\u003eC. 4-Imidazolines 372\u003c\/p\u003e \u003cp\u003eD. Heteroring-Substituted 2-Imiriaznliiics 372\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIII. Imidazolidines 373\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Alkyl- and Arylimidazolidines 373\u003c\/p\u003e \u003cp\u003eB. 4- and 5-Imidazolidones 378\u003c\/p\u003e \u003cp\u003eC. 2-Iraidazolidinethiones (Ethylenethioureas) 378\u003c\/p\u003e \u003cp\u003eD. 4-Imidazolidinethiones 379\u003c\/p\u003e \u003cp\u003eE. 2-Iminoimiriazoliriines (Ethyleneguanidines) 379\u003c\/p\u003e \u003cp\u003e\u003cb\u003eV. Benzimidazoles 379\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA. Alkyl- and Arylbenrimidazoles 379\u003c\/p\u003e \u003cp\u003eB. Alkyl- and Arylbenzimidazolium Salts 382\u003c\/p\u003e \u003cp\u003eC. Oxo-and Hydroxybenzimidazoles and Their Sulfur Analogues 382\u003c\/p\u003e \u003cp\u003eD. Halogeno-, Halogenoalkyl-, and Halogenoarylbenzimidazoles 388\u003c\/p\u003e \u003cp\u003eE. Nitro-, Nitroalkyl-, and Nitroarylbenzimidazoles Including Those Containing Additional Functional Groups 388\u003c\/p\u003e \u003cp\u003eF. Aminobenzimidazoles 389\u003c\/p\u003e \u003cp\u003eG. Cyanobenzimidazoles 394\u003c\/p\u003e \u003cp\u003eH Benzimidazolecarboxylic Acids 395\u003c\/p\u003e \u003cp\u003eI. Benzimidazolcsulfonic Acids, Sulfoalkyl-, and Sulfoarylbenzimidazoles 398\u003c\/p\u003e \u003cp\u003eJ. Benzimidazole Arscnicals 398\u003c\/p\u003e \u003cp\u003eK. 2,3-DihydroIxaizimidazoles (Benzimidizolines) 399\u003c\/p\u003e \u003cp\u003eL. Heteroring-Substituted Benzimidazoles 399\u003c\/p\u003e \u003cp\u003eM Bi-, Di-, and Bisbonzimidazoles 401\u003c\/p\u003e \u003cp\u003eBibliography 401\u003c\/p\u003e \u003cp\u003eSubject Index 421\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":52276212662552,"sku":"9780470376539","price":396.59,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470376539.jpg?v=1781365229","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/imidazole-and-its-derivatives-volume-6-part-1-hardback-9780470376539","provider":"Freshly Printed Books","version":"1.0","type":"link"}