{"product_id":"heterocyclic-compounds-with-indole-and-carbazole-systems-volume-8-hardback-9780470377192","title":"Heterocyclic Compounds with Indole and Carbazole Systems, Volume 8 (Hardback) 9780470377192","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eHeterocyclic Compounds with Indole and Carbazole Systems, Volume 8\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\"\u003eWard C. Sumpter (Author), F. M. Miller (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470377192, 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\"\u003e320 pages\u003cbr\u003e23.8 x 16.5 x 2.6 cm, 0.652 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\"\u003eThe \u003ci\u003eChemistry 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\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003e\u003cb\u003eI\u003c\/b\u003e\u003cb\u003e. Indole 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eIntroduction 1\u003c\/p\u003e \u003cp\u003eSynthesis of Indole 3\u003c\/p\u003e \u003cp\u003eOxidation of Indole 23\u003c\/p\u003e \u003cp\u003eTautomerism of Indole 25\u003c\/p\u003e \u003cp\u003eSulfonation of Indole 28\u003c\/p\u003e \u003cp\u003eHalogen Derivatives of Indole 29\u003c\/p\u003e \u003cp\u003eAlkyl Derivatives of Indole 31\u003c\/p\u003e \u003cp\u003eIndoline 36\u003c\/p\u003e \u003cp\u003eMetal Salts of Indole 40\u003c\/p\u003e \u003cp\u003eIndole Aldehydes 40\u003c\/p\u003e \u003cp\u003eAcyl Derivatives of Indole 44\u003c\/p\u003e \u003cp\u003eCondensation of Indoles with Aldehydes 48\u003c\/p\u003e \u003cp\u003eIndolylmagnesium Halides 50\u003c\/p\u003e \u003cp\u003eIndole Polymers 61\u003c\/p\u003e \u003cp\u003ePreparation and Reactions of Gramine 62\u003c\/p\u003e \u003cp\u003eCarboxylic Acids of the Indole Series 65\u003c\/p\u003e \u003cp\u003e\u003cb\u003eII\u003c\/b\u003e\u003cb\u003e. Carbazole 70\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eIntroduction 70\u003c\/p\u003e \u003cp\u003ePreparation of Carbazole 72\u003c\/p\u003e \u003cp\u003eGraebe-Ullman Synthesis 72\u003c\/p\u003e \u003cp\u003eMethod of Borsche 73\u003c\/p\u003e \u003cp\u003eOther Methods of Synthesis of Carbazoles 78\u003c\/p\u003e \u003cp\u003eNitro Derivatives of Carbazole 81\u003c\/p\u003e \u003cp\u003eAminocarbazoles 85\u003c\/p\u003e \u003cp\u003eHalogen Derivatives of Carbazole 87\u003c\/p\u003e \u003cp\u003eCarbazolesulfonic Acids 91\u003c\/p\u003e \u003cp\u003eReduction of Carbazole 93\u003c\/p\u003e \u003cp\u003eOxidation of Carbazole 96\u003c\/p\u003e \u003cp\u003eCarbazyl Aldehydes and Ketones 97\u003c\/p\u003e \u003cp\u003eCarbazole Carboxylic Acids 101\u003c\/p\u003e \u003cp\u003eN-Acyl Carbazoles 104\u003c\/p\u003e \u003cp\u003eN-Alkyl Carbazoles 105\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIII\u003c\/b\u003e\u003cb\u003e. Isatin 110\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003ePreparation of Isatin 111\u003c\/p\u003e \u003cp\u003eProperties of Isatin 114\u003c\/p\u003e \u003cp\u003eTautomerism 115\u003c\/p\u003e \u003cp\u003eReactions of Isatin 116\u003c\/p\u003e \u003cp\u003eOxidation and Reduction 116\u003c\/p\u003e \u003cp\u003eHalogenation and Nitration 118\u003c\/p\u003e \u003cp\u003eAcylation and Alkylation 120\u003c\/p\u003e \u003cp\u003eReactions of the Carbonyl Groups 121\u003c\/p\u003e \u003cp\u003eGrignard Reagents 121\u003c\/p\u003e \u003cp\u003eAmine Derivatives 122\u003c\/p\u003e \u003cp\u003eMiscellaneous Reagents 126\u003c\/p\u003e \u003cp\u003eActive Methylene Groups 127\u003c\/p\u003e \u003cp\u003eBiological Activity of Isatin 132\u003c\/p\u003e \u003cp\u003eAnalytical Uses of Isatin 133\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIV\u003c\/b\u003e\u003cb\u003e. Oxindole 134\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003ePreparation of Oxindoles 134\u003c\/p\u003e \u003cp\u003eProperties of Oxindoles 138\u003c\/p\u003e \u003cp\u003eTautomerism 138\u003c\/p\u003e \u003cp\u003eSalts 138\u003c\/p\u003e \u003cp\u003eReactions of Oxindole 139\u003c\/p\u003e \u003cp\u003eReduction 139\u003c\/p\u003e \u003cp\u003eHalogenation and Nitration 140\u003c\/p\u003e \u003cp\u003eCondensation Reactions 142\u003c\/p\u003e \u003cp\u003eAlkylation and Acylation 146\u003c\/p\u003e \u003cp\u003eDerivatives 148\u003c\/p\u003e \u003cp\u003eHydroxyoxindoles 148\u003c\/p\u003e \u003cp\u003eDioxindole 148\u003c\/p\u003e \u003cp\u003e1 -Hydroxyoxindole 151\u003c\/p\u003e \u003cp\u003eAminooxindoles 151\u003c\/p\u003e \u003cp\u003e3, 3-Diaryloxindoles 152\u003c\/p\u003e \u003cp\u003e\u003cb\u003eV\u003c\/b\u003e\u003cb\u003e. Isatogens 154\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVI\u003c\/b\u003e\u003cb\u003e. Indoxyl 163\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eIntroduction 163\u003c\/p\u003e \u003cp\u003eSynthesis of Indoxyl 163\u003c\/p\u003e \u003cp\u003ePhysical Properties 165\u003c\/p\u003e \u003cp\u003eReactions 165\u003c\/p\u003e \u003cp\u003eAcyl Derivatives of Intloxyl 167\u003c\/p\u003e \u003cp\u003eIndoxyl Sulfuric Acid 168\u003c\/p\u003e \u003cp\u003eIndican 168\u003c\/p\u003e \u003cp\u003eIndoxylic Acid and Indoxyl-2-aldehyde 169\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVII\u003c\/b\u003e\u003cb\u003e. Indigo 171\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eIntroduction 171\u003c\/p\u003e \u003cp\u003eOccurrence of Indigo 174\u003c\/p\u003e \u003cp\u003eSynthesis of Indigo 175\u003c\/p\u003e \u003cp\u003ePhysical Properties of Indigo 178\u003c\/p\u003e \u003cp\u003eChemical Properties of Indigo 179\u003c\/p\u003e \u003cp\u003eFormation of Salts 179\u003c\/p\u003e \u003cp\u003eOxidation of Indigo 180\u003c\/p\u003e \u003cp\u003eImides and Oximes of Indigo 181\u003c\/p\u003e \u003cp\u003eReduction of Indigo 182\u003c\/p\u003e \u003cp\u003eHalogenated Indigos 184\u003c\/p\u003e \u003cp\u003eAlkyl and Acyl Derivatives of Indigo 189\u003c\/p\u003e \u003cp\u003ePreparation of Indigoids 191\u003c\/p\u003e \u003cp\u003eIsoindigo and Indirubin 192\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVIII\u003c\/b\u003e\u003cb\u003e. Natural Products Containing the Indole Nucleus 196\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eSimple Bases 196\u003c\/p\u003e \u003cp\u003eGramine 196\u003c\/p\u003e \u003cp\u003eDonaxarine 197\u003c\/p\u003e \u003cp\u003eTryptophan 197\u003c\/p\u003e \u003cp\u003eSerotonin 199\u003c\/p\u003e \u003cp\u003eAbrine 200\u003c\/p\u003e \u003cp\u003eHypaphorine 200\u003c\/p\u003e \u003cp\u003eBufotenines 201\u003c\/p\u003e \u003cp\u003eDipterine 202\u003c\/p\u003e \u003cp\u003eCalabar Alkaloids 203\u003c\/p\u003e \u003cp\u003ePhysostigmine 203\u003c\/p\u003e \u003cp\u003eGeneserine 207\u003c\/p\u003e \u003cp\u003e\u003ci\u003eHarmala \u003c\/i\u003eAlkaloids 208\u003c\/p\u003e \u003cp\u003eHarmaline, Harmine, and Harmalol 208\u003c\/p\u003e \u003cp\u003eHarman 213\u003c\/p\u003e \u003cp\u003eEleaginine 213\u003c\/p\u003e \u003cp\u003eLeptocladine 213\u003c\/p\u003e \u003cp\u003eCalycanthine 214\u003c\/p\u003e \u003cp\u003eCalycanthidine 216\u003c\/p\u003e \u003cp\u003eFolicanthine 217\u003c\/p\u003e \u003cp\u003e\u003ci\u003eEvodia \u003c\/i\u003eAlkaloids 218\u003c\/p\u003e \u003cp\u003eEvodiaminu 218\u003c\/p\u003e \u003cp\u003eRutecarpine 218\u003c\/p\u003e \u003cp\u003e\u003ci\u003eCinchona \u003c\/i\u003eAlkaloids 220\u003c\/p\u003e \u003cp\u003eCinchonamine 221\u003c\/p\u003e \u003cp\u003eQuinamine 222\u003c\/p\u003e \u003cp\u003e\u003ci\u003eYohinzbe \u003c\/i\u003ehlkaloids 223\u003c\/p\u003e \u003cp\u003eYohimbine 224\u003c\/p\u003e \u003cp\u003eCorynantheine 233\u003c\/p\u003e \u003cp\u003eCorynantheidine 234\u003c\/p\u003e \u003cp\u003eQuebracho Alkaloids 234\u003c\/p\u003e \u003cp\u003eAspidospermine 234\u003c\/p\u003e \u003cp\u003eVallesine 235\u003c\/p\u003e \u003cp\u003eQuebrachamine 235\u003c\/p\u003e \u003cp\u003eCalabash Curare Alkaloids 235\u003c\/p\u003e \u003cp\u003eAlstonilidine 238\u003c\/p\u003e \u003cp\u003eGelsemium Alkaloids 240\u003c\/p\u003e \u003cp\u003e\u003ci\u003eAlslonia \u003c\/i\u003eAlkaloids 238\u003c\/p\u003e \u003cp\u003eAlstonine 238\u003c\/p\u003e \u003cp\u003eGelsemine 240\u003c\/p\u003e \u003cp\u003eSempervirine 242\u003c\/p\u003e \u003cp\u003eGelsemicine 244\u003c\/p\u003e \u003cp\u003e\u003ci\u003eRauwdfia \u003c\/i\u003eAlkaloids 244\u003c\/p\u003e \u003cp\u003eRauwolscine 245\u003c\/p\u003e \u003cp\u003e\u003ci\u003eGcissospevinzrm \u003c\/i\u003eAlkaloids 247\u003c\/p\u003e \u003cp\u003eStrychnos Alkaloids 257\u003c\/p\u003e \u003cp\u003eStrychnine and Rrucine 258\u003c\/p\u003e \u003cp\u003e\u003ci\u003eα\u003c\/i\u003e- and \u003ci\u003eβ\u003c\/i\u003e-Colubrine 275\u003c\/p\u003e \u003cp\u003eHolstiine 275\u003c\/p\u003e \u003cp\u003eMold Products 276\u003c\/p\u003e \u003cp\u003eCliotoxin 276\u003c\/p\u003e \u003cp\u003eMelanine; Aminochrom2s 278\u003c\/p\u003e \u003cp\u003eMinor Alkaloids 279\u003c\/p\u003e \u003cp\u003eUncaria Alkaloids 280\u003c\/p\u003e \u003cp\u003eAjmaline 244\u003c\/p\u003e \u003cp\u003eSerpentine 246\u003c\/p\u003e \u003cp\u003eGeissospermine 247\u003c\/p\u003e \u003cp\u003eErgot Alkaloids 248\u003c\/p\u003e \u003cp\u003eVomicine 270\u003c\/p\u003e \u003cp\u003eStrychnospermine 275\u003c\/p\u003e \u003cp\u003eChetomin 278\u003c\/p\u003e \u003cp\u003eKarnassine 280\u003c\/p\u003e \u003cp\u003e13iogencsis 281\u003c\/p\u003e \u003cp\u003eAbsorption Spectra of Indole I3ascj 284\u003c\/p\u003e \u003cp\u003eIndex 288\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":52276212793624,"sku":"9780470377192","price":430.19,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470377192.jpg?v=1781365230","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/heterocyclic-compounds-with-indole-and-carbazole-systems-volume-8-hardback-9780470377192","provider":"Freshly Printed Books","version":"1.0","type":"link"}