{"product_id":"quinoxalines-spplement-2-61-chemistry-of-heterocyclic-compounds-a-series-of-monographs-9780471264958","title":"Quinoxalines Spplement 2 61 Chemistry of","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eReviews various quinoxaline literature from 1975 onwards, designed for use in conjuction with earlier reviews.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTrade Review\u003c\/b\u003e\u003cbr\u003e\"This book updates Volumes 5 and 35 of this series on quinoxalines and covers the literature on quinoxalines from approximately 1976-2002.\" (\u003ci\u003eJournal of the American Chemical Society\u003c\/i\u003e, June 9, 2004)\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cp\u003e\u003cb\u003eChapter 1 Primary Syntheses 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 From a Single Benzene Substrate 1\u003c\/p\u003e \u003cp\u003e1.1.1 By Formation of the N1,C8a Bond 1\u003c\/p\u003e \u003cp\u003e1.1.2 By Formation of the N1,C2 Bond 4\u003c\/p\u003e \u003cp\u003e1.1.2.1 Cyclization of \u003ci\u003eo\u003c\/i\u003e-(Ethylamino)aniline Derivatives 4\u003c\/p\u003e \u003cp\u003e1.1.2.2 Direct Cyclization of \u003ci\u003eo\u003c\/i\u003e-(Ethylamino)nitrobenzene Derivatives 6\u003c\/p\u003e \u003cp\u003e1.1.2.3 Reductive Cyclization of \u003ci\u003eo\u003c\/i\u003e-(Ethylamino)nitrobenzene Derivatives 8\u003c\/p\u003e \u003cp\u003e1.1.3 By Formation of the C2,C3 Bond 12\u003c\/p\u003e \u003cp\u003e1.2 From a Benzene Substrate with an Ancillary Synthon 13\u003c\/p\u003e \u003cp\u003e1.2.1 When the Synthon Supplies N1 of the Quinoxaline 13\u003c\/p\u003e \u003cp\u003e1.2.2 When the Synthon Supplies C2 of the Quinoxaline 14\u003c\/p\u003e \u003cp\u003e1.2.3 When the Synthon Supplies C2 + C3 of the Quinoxaline 16\u003c\/p\u003e \u003cp\u003e1.2.3.1 Using a Dialdehyde (Glyoxal) or Related Synthon 16\u003c\/p\u003e \u003cp\u003e1.2.3.2 Using an Aldehydo Ketone or Related Synthon 18\u003c\/p\u003e \u003cp\u003e1.2.3.3 Using an Aldehydo Acid or Related Synthon 22\u003c\/p\u003e \u003cp\u003e1.2.3.4 Using an Aldehydo Ester or Related Synthon 23\u003c\/p\u003e \u003cp\u003e1.2.3.5 Using an Aldehydo Amide, Nitrile, Acyl Halide, or Related Synthon 24\u003c\/p\u003e \u003cp\u003e1.2.3.6 Using a Diketone or Related Synthon 24\u003c\/p\u003e \u003cp\u003e1.2.3.7 Using a Keto Acid or Related Synthon 30\u003c\/p\u003e \u003cp\u003e1.2.3.8 Using a Keto Ester or Related Synthon 31\u003c\/p\u003e \u003cp\u003e1.2.3.9 Using a Keto Amide, Nitrile, Acyl Halide, or Related Synthon 34\u003c\/p\u003e \u003cp\u003e1.2.3.10 Using a Diacid (Oxalic Acid) as Synthon 35\u003c\/p\u003e \u003cp\u003e1.2.3.11 Using a Diester (a Dialkyl Oxalate) or Related Synthon 36\u003c\/p\u003e \u003cp\u003e1.2.3.12 Using an Estero Amide, Nitrile, Acyl Halide, or Related Synthon 38\u003c\/p\u003e \u003cp\u003e1.2.3.13 Using a Diamide (Oxamide), Amido Nitrile, or Related Synthon 40\u003c\/p\u003e \u003cp\u003e1.2.3.14 Using a Diacyl Dihalide (Oxalyl Halide) or Related Synthon 40\u003c\/p\u003e \u003cp\u003e1.2.4 When the Synthon Supplies N1 + C2 + C3 of the Quinoxaline 42\u003c\/p\u003e \u003cp\u003e1.2.5 When the Synthon Supplies N1 + C2 + C3 + N4 of the Quinoxaline 42\u003c\/p\u003e \u003cp\u003e1.3 From a Benzene Substrate with Two or More Synthons 44     \u003c\/p\u003e \u003cp\u003e1.4 From a Pyrazine Substrate with or without Synthon(s) 45\u003c\/p\u003e \u003cp\u003e1.5 From Other Heteromonocyclic Substrates\/Synthons 46\u003c\/p\u003e \u003cp\u003e1.5.1 Azirines as Substrates\/Synthons 47\u003c\/p\u003e \u003cp\u003e1.5.2 1,2,3-Dithiazol-1-iums as Substrates\/Synthons 47\u003c\/p\u003e \u003cp\u003e1.5.3 Furans as Substrates\/Synthons 48\u003c\/p\u003e \u003cp\u003e1.5.4 Isothiazoles as Substrates\/Synthons 49\u003c\/p\u003e \u003cp\u003e1.5.5 Isoxazoles as Substrates\/Synthons 50\u003c\/p\u003e \u003cp\u003e1.5.6 Oxazoles as Substrates\/Synthons 51\u003c\/p\u003e \u003cp\u003e1.5.7 Oxirenes as Substrates\/Synthons 51\u003c\/p\u003e \u003cp\u003e1.5.8 Pyrans as Substrates\/Synthons 53\u003c\/p\u003e \u003cp\u003e1.5.9 Pyridazines as Substrates\/Synthons 53\u003c\/p\u003e \u003cp\u003e1.5.10 Pyridines as Substrates\/Synthons 54\u003c\/p\u003e \u003cp\u003e1.5.11 Pyrimidines as Substrates\/Synthons 54\u003c\/p\u003e \u003cp\u003e1.5.12 Pyrroles as Substrates\/Synthons 55\u003c\/p\u003e \u003cp\u003e1.5.13 Thiophenes as Substrates\/Synthons 55\u003c\/p\u003e \u003cp\u003e1.5.14 1,2,4-Triazines as Substrates\/Synthons 56\u003c\/p\u003e \u003cp\u003e1.5.15 1,2,3-Triazoles as Substrates\/Synthons 56\u003c\/p\u003e \u003cp\u003e1.6 From Heterobicyclic Substrates\/Synthons 57\u003c\/p\u003e \u003cp\u003e1.6.1 7-Azabicyclo[4.1.0]heptanes as Substrates\/Synthons 57\u003c\/p\u003e \u003cp\u003e1.6.2 Benzimidazoles as Substrates\/Synthons 57\u003c\/p\u003e \u003cp\u003e1.6.3 1,4-Benzodiazepines as Substrates\/Synthons 59\u003c\/p\u003e \u003cp\u003e1.6.4 1,5-Benzodiazepines as Substrates\/Synthons 59\u003c\/p\u003e \u003cp\u003e1.6.5 1-Benzopyrans (Chromenes) as Substrates\/Synthons 61\u003c\/p\u003e \u003cp\u003e1.6.6 2,1,3-Benzoselena(or thia)diazoles as Substrates\/Synthons 61\u003c\/p\u003e \u003cp\u003e1.6.7 2,1,3-Benzoxadiazoles as Substrates\/Synthons 62\u003c\/p\u003e \u003cp\u003e1.6.8 Cycloheptapyrazines as Substrates\/Synthons 68\u003c\/p\u003e \u003cp\u003e1.6.9 Indoles as Substrates\/Synthons 68\u003c\/p\u003e \u003cp\u003e1.6.10 Pyrrolo[3,4-\u003ci\u003eb\u003c\/i\u003e]pyrazines as Substrates\/Synthons 69\u003c\/p\u003e \u003cp\u003e1.7 From Heteropolycyclic Substrates\/Synthons 70\u003c\/p\u003e \u003cp\u003e1.7.1 Azeto- or Azirino[1,2-\u003ci\u003ea\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 70\u003c\/p\u003e \u003cp\u003e1.7.2 Benz[\u003ci\u003eg\u003c\/i\u003e]indoles as Substrates\/Synthons 71\u003c\/p\u003e \u003cp\u003e1.7.3 Benzo[3,4]cyclobuta[1,2-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 71\u003c\/p\u003e \u003cp\u003e1.7.4 Benzo[\u003ci\u003eg\u003c\/i\u003e]pteridines as Substrates\/Synthons 71\u003c\/p\u003e \u003cp\u003e1.7.5 [1]Benzopyrano[2,3-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 73\u003c\/p\u003e \u003cp\u003e1.7.6 [1]Benzothiopyrano[4,3-\u003ci\u003eb\u003c\/i\u003e]pyrroles as Substrates\/Synthons 73\u003c\/p\u003e \u003cp\u003e1.7.7 Cyclobuta[\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 73\u003c\/p\u003e \u003cp\u003e1.7.8 1,3-Dithiolo[4,5-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 74\u003c\/p\u003e \u003cp\u003e1.7.9 1,4-Ethanoquinoxalines as Substrates\/Synthons 74\u003c\/p\u003e \u003cp\u003e1.7.10 Furo[2,3-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 75\u003c\/p\u003e \u003cp\u003e1.7.11 Furo[3,4-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 76\u003c\/p\u003e \u003cp\u003e1.7.12 Indeno[1,2-\u003ci\u003eb\u003c\/i\u003e]pyrroles as Substrates\/Synthons 76\u003c\/p\u003e \u003cp\u003e1.7.13 Isoxazolo[2,3-\u003ci\u003ed\u003c\/i\u003e][1,4]benzodiazepines as Substrates\/Synthons 77\u003c\/p\u003e \u003cp\u003e1.7.14 Isoxazolo[2,3-\u003ci\u003ea\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 77\u003c\/p\u003e \u003cp\u003e1.7.15 [1,3,4]Oxadiazino[5,6-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 78\u003c\/p\u003e \u003cp\u003e1.7.16 [1,2,4]Oxadiazolo[2,3-\u003ci\u003ea\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 78\u003c\/p\u003e \u003cp\u003e1.7.17 [1,2,5]Oxadiazolo[3,4-\u003ci\u003ef\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 79\u003c\/p\u003e \u003cp\u003e1.7.18 Phenazines as Substrates\/Synthons 79\u003c\/p\u003e \u003cp\u003e1.7.19 Pyrazolo[3,4-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 79\u003c\/p\u003e \u003cp\u003e1.7.20 Pyridazino[4,5-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 80\u003c\/p\u003e \u003cp\u003e1.7.21 Pyrrolo[3,4-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 81\u003c\/p\u003e \u003cp\u003e1.7.22 Quinoxalino[2,3-\u003ci\u003eb\u003c\/i\u003e]quinoxalines as Substrates\/Synthons 82\u003c\/p\u003e \u003cp\u003e1.7.23 Thiazolo[2,3-\u003ci\u003eb\u003c\/i\u003e]benzothiazoliums as Substrates\/Synthons 82\u003c\/p\u003e \u003cp\u003e1.7.24 Thiazolo[3,2-\u003ci\u003ea\u003c\/i\u003e]quinoxaliniums as Substrates\/Synthons 82\u003c\/p\u003e \u003cp\u003e1.8 From Spiro Heterocyclic Substrates 83\u003c\/p\u003e \u003cp\u003e1.9 Glance Index to Typical Quinoxaline Derivatives Available by Primary Syntheses 84\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 2 Quinoxaline, Alkylquinoxalines, And Arylquinoxalines 93\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Quinoxaline 93\u003c\/p\u003e \u003cp\u003e2.1.1 Preparation of Quinoxaline 93\u003c\/p\u003e \u003cp\u003e2.1.2 Properties of Quinoxaline 94\u003c\/p\u003e \u003cp\u003e2.1.3 Reactions of Quinoxaline 95\u003c\/p\u003e \u003cp\u003e2.2 Alkyl- and Arylquinoxalines 100\u003c\/p\u003e \u003cp\u003e2.2.1 Preparation of \u003ci\u003eC\u003c\/i\u003e-Alkyl- and \u003ci\u003eC\u003c\/i\u003e-Arylquinoxalines 101\u003c\/p\u003e \u003cp\u003e2.2.1.1 By Direct Alkylation or Arylation 101\u003c\/p\u003e \u003cp\u003e2.2.1.2 By Alkanelysis or Arenelysis of Halogenoquinoxalines 102\u003c\/p\u003e \u003cp\u003e2.2.1.3 From \u003ci\u003eC\u003c\/i\u003e-Formyl-, \u003ci\u003eC\u003c\/i\u003e-Aroyl-, \u003ci\u003eC\u003c\/i\u003e-Cyano-, or Oxoquinoxalines 106\u003c\/p\u003e \u003cp\u003e2.2.1.4 By Interconversion of Alkyl or Aryl Substituents 108\u003c\/p\u003e \u003cp\u003e2.2.1.5 By Elimination of Functionality from Substituted-Alkyl Substituents 113\u003c\/p\u003e \u003cp\u003e2.2.2 Preparation of \u003ci\u003eN\u003c\/i\u003e-Alkyl or \u003ci\u003eN\u003c\/i\u003e-Aryl Derivatives of Hydroquinoxalines 114\u003c\/p\u003e \u003cp\u003e2.2.3 Properties of Alkyl- and Arylquinoxalines 115\u003c\/p\u003e \u003cp\u003e2.2.4 Reactions of Alkyl- and Arylquinoxalines 117\u003c\/p\u003e \u003cp\u003e2.3 N-Alkylquinoxalinium Salts 129\u003c\/p\u003e \u003cp\u003e2.3.1 Preparation of \u003ci\u003eN\u003c\/i\u003e-Alkylquinoxalinium Salts 129\u003c\/p\u003e \u003cp\u003e2.3.2 Reactions of \u003ci\u003eN\u003c\/i\u003e-Alkylquinoxalinium Salts 131\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 3 Halogenoquinoxalines 133\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Preparation of Nuclear Halogenoquinoxalines 133\u003c\/p\u003e \u003cp\u003e3.1.1 Nuclear Halogenoquinoxalines from Quinoxalinones 133\u003c\/p\u003e \u003cp\u003e3.1.2 Nuclear Halogenoquinoxalines by Direct Halogenation 139\u003c\/p\u003e \u003cp\u003e3.1.3 Nuclear Halogenoquinoxalines from Quinoxalinamines 141\u003c\/p\u003e \u003cp\u003e3.1.4 Nuclear Halogenoquinoxalines by Transhalogenation 142\u003c\/p\u003e \u003cp\u003e3.1.5 Nuclear Halogenoquinoxalines from Miscellaneous Substrates 144\u003c\/p\u003e \u003cp\u003e3.2 Reactions of Nuclear Halogenoquinoxalines 146\u003c\/p\u003e \u003cp\u003e3.2.1 Aminolysis of Nuclear Halogenoquinoxalines 146\u003c\/p\u003e \u003cp\u003e3.2.2 Hydrolysis, Alcoholysis, or Phenolysis of Nuclear Halogenoquinoxalines 156\u003c\/p\u003e \u003cp\u003e3.2.3 Thiolysis, Alkanethiolysis, Arenethiolysis, or Arenesulfinolysis of Nuclear Halogenoquinoxalines 161\u003c\/p\u003e \u003cp\u003e3.2.4 Azidolysis of Nuclear Halogenoquinoxalines 164\u003c\/p\u003e \u003cp\u003e3.2.5 Cyanolysis of Nuclear Halogenoquinoxalines 166\u003c\/p\u003e \u003cp\u003e3.2.6 Hydrogenolysis of Nuclear Halogenoquinoxalines 167\u003c\/p\u003e \u003cp\u003e3.2.7 Other Displacement Reactions of Nuclear Halogenoquinoxalines 168\u003c\/p\u003e \u003cp\u003e3.2.8 Cyclization Reactions of Nuclear Halogenoquinoxalines 170\u003c\/p\u003e \u003cp\u003e3.3 Preparation of Extranuclear Halogenoquinoxalines 174\u003c\/p\u003e \u003cp\u003e3.4 Reactions of Extranuclear Halogenoquinoxalines 175\u003c\/p\u003e \u003cp\u003e3.4.1 Aminolysis of Extranuclear Halogenoquinoxalines 175\u003c\/p\u003e \u003cp\u003e3.4.2 Hydrolysis, Alcoholysis, or Phenolysis of Extranuclear Halogenoquinoxalines 179\u003c\/p\u003e \u003cp\u003e3.4.3 Acyloxy Derivatives from Extranuclear Halogenoquinoxalines 181\u003c\/p\u003e \u003cp\u003e3.4.4 Thiolysis, Alkanethiolysis, Arenethiolysis, or Arenesulfinolysis of Extranuclear Halogenoquinoxalines 183\u003c\/p\u003e \u003cp\u003e3.4.5 Other Displacement Reactions of Extranuclear Halogenoquinoxalines 184\u003c\/p\u003e \u003cp\u003e3.4.6 Cyclization Reactions of Extranuclear Halogenoquinoxalines 186\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 4 Oxyquinoxalines 189\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Tautomeric Quinoxalinones 189\u003c\/p\u003e \u003cp\u003e4.1.1 Preparation of Tautomeric Quinoxalinones 190\u003c\/p\u003e \u003cp\u003e4.1.2 Reactions of Tautomeric Quinoxalinones 194\u003c\/p\u003e \u003cp\u003e4.1.2.1 Conversion into Quinoxalinethiones 195\u003c\/p\u003e \u003cp\u003e4.1.2.2 Conversion into O- and\/or N-Alkylated Derivatives 195\u003c\/p\u003e \u003cp\u003e4.1.2.3 Miscellaneous Reactions 200\u003c\/p\u003e \u003cp\u003e4.2 Quinoxalinequinones 206\u003c\/p\u003e \u003cp\u003e4.2.1 Preparation of Quinoxalinequinones 206\u003c\/p\u003e \u003cp\u003e4.2.2 Reactions of Quinoxalinequinones 208\u003c\/p\u003e \u003cp\u003e4.3 Extranuclear Hydroxyquinoxalines 211\u003c\/p\u003e \u003cp\u003e4.3.1 Preparation of Extranuclear Hydroxyquinoxalines 212\u003c\/p\u003e \u003cp\u003e4.3.2 Reactions of Extranuclear Hydroxyquinoxalines 215\u003c\/p\u003e \u003cp\u003e4.4 Alkoxy- and Aryloxyquinoxalines 219\u003c\/p\u003e \u003cp\u003e4.4.1 Preparation of Alkoxy- and Aryloxyquinoxalines 219\u003c\/p\u003e \u003cp\u003e4.4.2 Reactions of Alkoxy- and Aryloxyquinoxalines 221\u003c\/p\u003e \u003cp\u003e4.5 Nontautomeric Quinoxalinones 223\u003c\/p\u003e \u003cp\u003e4.5.1 Preparation of Nontautomeric Quinoxalinones 223\u003c\/p\u003e \u003cp\u003e4.5.2 Reactions of Nontautomeric Quinoxalinones 224\u003c\/p\u003e \u003cp\u003e4.6 Quinoxaline N-Oxides 225\u003c\/p\u003e \u003cp\u003e4.6.1 Preparation of Quinoxaline N-Oxides 226\u003c\/p\u003e \u003cp\u003e4.6.2 Reactions of Quinoxaline N-Oxides 230\u003c\/p\u003e \u003cp\u003e4.6.2.1 Deoxygenation 230\u003c\/p\u003e \u003cp\u003e4.6.2.2 Deoxidative C-Substitutions 235\u003c\/p\u003e \u003cp\u003e4.6.2.3 Other Reactions 237\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 5 Thioquinoxalines 241\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Quinoxalinethiones and Quinoxalinethiols 241\u003c\/p\u003e \u003cp\u003e5.1.1 Preparation of Quinoxalinethiones and Quinoxalinethiols 241\u003c\/p\u003e \u003cp\u003e5.1.2 Reactions of Quinoxalinethiones and Quinoxalinethiols 242\u003c\/p\u003e \u003cp\u003e5.2 Alkylthioquinoxalines and Diquinoxalinyl Sulfides 246\u003c\/p\u003e \u003cp\u003e5.2.1 Preparation of Alkylthioquinoxalines 246\u003c\/p\u003e \u003cp\u003e5.2.2 Reactions of Alkylthioquinoxalines 248\u003c\/p\u003e \u003cp\u003e5.3 Diquinoxalinyl Disulfides and Quinoxalinesulfonic Acid Derivatives 250\u003c\/p\u003e \u003cp\u003e5.4 Quinoxaline Sulfoxides and Sulfones 251\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 6 Nitro-, Amino-, and Related Quinoxalines 255\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Nitroquinoxalines 255\u003c\/p\u003e \u003cp\u003e6.1.1 Preparation of Nitroquinoxalines 255\u003c\/p\u003e \u003cp\u003e6.1.1.1 By Direct Nitration 255\u003c\/p\u003e \u003cp\u003e6.1.1.2 From Dimethylsulfimidoquinoxalines 260\u003c\/p\u003e \u003cp\u003e6.1.2 Reactions of Nitroquinoxalines 260\u003c\/p\u003e \u003cp\u003e6.1.2.1 Reduction to Quinoxalinamines 260\u003c\/p\u003e \u003cp\u003e6.1.2.2 Displacement Reactions 265\u003c\/p\u003e \u003cp\u003e6.2 Nitrosoquinoxalines 267\u003c\/p\u003e \u003cp\u003e6.3 Regular Aminoquinoxalines 269\u003c\/p\u003e \u003cp\u003e6.3.1 Preparation of Regular Aminoquinoxalines 269\u003c\/p\u003e \u003cp\u003e6.3.2 Reactions of Regular Aminoquinoxalines 278\u003c\/p\u003e \u003cp\u003e6.3.2.1 \u003ci\u003eN\u003c\/i\u003e-Acylation of Aminoquinoxalines or Reduced Quinoxalines 279\u003c\/p\u003e \u003cp\u003e6.3.2.2 \u003ci\u003eN\u003c\/i\u003e-Alkylation or Alkylidenation of Aminoquinoxalines 283\u003c\/p\u003e \u003cp\u003e6.3.2.3 Reactions Involving Initial Diazotization of Aminoquinoxalines 286\u003c\/p\u003e \u003cp\u003e6.3.2.4 Miscellaneous Transformations of Aminoquinoxalines 288\u003c\/p\u003e \u003cp\u003e6.3.2.5 Cyclization of Aminoquinoxalines 291\u003c\/p\u003e \u003cp\u003e6.4 Hydrazino- and Hydrazonoquinoxalines 296\u003c\/p\u003e \u003cp\u003e6.4.1 Preparation of Hydrazino- and Hydrazonoquinoxalines 297\u003c\/p\u003e \u003cp\u003e6.4.2 Reactions of Hydrazino- and Hydrazonoquinoxalines 299\u003c\/p\u003e \u003cp\u003e6.4.2.1 Noncyclization Reactions 300\u003c\/p\u003e \u003cp\u003e6.4.2.2 Cyclization Reactions 305\u003c\/p\u003e \u003cp\u003e6.5 Azidoquinoxalines 312\u003c\/p\u003e \u003cp\u003e6.6 Arylazoquinoxalines 314\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 7 Quinoxalinecarboxylic Acids And Related Derivatives 317\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 Quinoxalinecarboxylic Acids and Anhydrides 317\u003c\/p\u003e \u003cp\u003e7.1.1 Preparation of Quinoxalinecarboxylic Acids 317\u003c\/p\u003e \u003cp\u003e7.1.2 Reactions of Quinoxalinecarboxylic Acids 322\u003c\/p\u003e \u003cp\u003e7.2 Quinoxalinecarboxylic Esters 327\u003c\/p\u003e \u003cp\u003e7.2.1 Preparation of Quinoxalinecarboxylic Esters 327\u003c\/p\u003e \u003cp\u003e7.2.2 Reactions of Quinoxalinecarboxylic Esters 329\u003c\/p\u003e \u003cp\u003e7.3 Quinoxalinecarbonyl Halides 333\u003c\/p\u003e \u003cp\u003e7.4 Quinoxalinecarboxamides and Related Derivatives 334\u003c\/p\u003e \u003cp\u003e7.4.1 Preparation of Quinoxalinecarboxamides and the Like 335\u003c\/p\u003e \u003cp\u003e7.4.2 Reactions of Quinoxalinecarboxamides and the Like 337\u003c\/p\u003e \u003cp\u003e7.5 Quinoxalinecarbonitriles 342\u003c\/p\u003e \u003cp\u003e7.5.1 Preparation of Quinoxalinecarbonitriles 342\u003c\/p\u003e \u003cp\u003e7.5.2 Reactions of Quinoxalinecarbonitriles 343\u003c\/p\u003e \u003cp\u003e7.6 Quinoxalinecarbaldehydes 345\u003c\/p\u003e \u003cp\u003e7.6.1 Preparation of Quinoxalinecarbaldehydes 346\u003c\/p\u003e \u003cp\u003e7.6.2 Reactions of Quinoxalinecarbaldehydes 348\u003c\/p\u003e \u003cp\u003e7.7 Quinoxaline Ketones 352\u003c\/p\u003e \u003cp\u003e7.7.1 Preparation of Quinoxaline Ketones 352\u003c\/p\u003e \u003cp\u003e7.7.2 Reactions of Quinoxaline Ketones 353\u003c\/p\u003e \u003cp\u003e7.8 Quinoxaline Cyanates, Isocyanates, Thiocyanates, Isothiocyanates, and Nitrones 356\u003c\/p\u003e \u003cp\u003eAppendix: Table of Simple Quinoxalines 359\u003c\/p\u003e \u003cp\u003eReferences 437\u003c\/p\u003e \u003cp\u003eIndex 471\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default 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