Del 66 i serien Chemistry of Heterocyclic Compounds: A Series of Monographs

Six-Membered Heterocyclic Nitrogen Compounds with Four Condensed Rings, Volume 2

Inbunden, Engelska, 2007

8 879 kr

Beställningsvara. Skickas inom 5-8 vardagar. Fri frakt för medlemmar vid köp för minst 249 kr.

The Chemistry of Heterocyclic Compounds, 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.

Produktinformation

Utgivningsdatum2007-06-27
Mått157 x 235 x 26 mm
Vikt1 219 g
FormatInbunden
SpråkEngelska
SerieChemistry of Heterocyclic Compounds: A Series of Monographs
Antal sidor360
Upplaga91099
FörlagJohn Wiley & Sons Inc
ISBN9780470375211

Tillhör följande kategorier

Organisk kemi inom Naturvetenskap och teknik

Introduction 1I. Azanaphthacencs 3By Eleanor R. Webster1. Monoazanaphthacenes 3A. 1-Azanaphthacenc 3B. 2-Azanaphthacene 7C. 5-Azanaphthacene 82. Diazanaphthacenes 21A. 1,3-Diazanaphthacene 21B. 1,4-Diazanaphthacene 24C. 1,11-Diazanaphthacene 26D. 2,3-Diazanaphthacene 26E. 5,6-Diazanaphthacene 27F. 5,11-Diazanaphthacene 34G. 5,12-Diazanaphthacene 373. Triazanaphthacenes 43A. 1,6,11 -Triazanaphthacene 43B. 5,6,11-Triazanaphthacene 454. Tetrazanaphthacenes 45A. 1,3,5,12-Tetrazanaphthacene 45B. 1,4,6,11-Tetrazanaphthacene 47C. 5,6,11,12-Tetrazanaphthacene 50II. Azabenz[a]anthracenes 57By Jean V. Crawjard and Eleanor K. Webster1. Monoazabenz [a]anthracenes 57A. 1-Azabenz [a]anthracene 57B. 4-Azabenz[a]anthracene 61(1) Alkyl Derivatives 65(2) Oxidation Products 66(3) Halogen Derivatives 67(4) Nitro Derivatives 68(5) Sulfonated and Hydroxylated Derivatives 68(6) Physical Properties 73(7) Amino Compounds 75C. 5-Azabenz[a]anthracene 83D. 8-Azabenz[a]anthracene 85E. 10-Azabenz[a]anthracene 88F. 11-Azabcnz [a]anthracene 892. Diazabenz [a]anthracenes 91A. 1,3-Diazabenz[a]anthracene 91B. 1,4-Diazabenz [a]anthracene 93C. 1,7-Diazabenz [a]anthracene 96D. 1,12-Diazabenz [a]anthracene 96E. 2,4-Diazabenz [a]anthracene 98F. 4,7-Diazabenz [a]anthracene 99G. 4,12-Diazabcnz [a]anthracene 100H. 5,7-Diazabenz [a]anthracene 101(1) Ciba Yellow 3G 102(2) Hochst Yellow U 10713) Hochst Yellow R 109I. 5,12-Diazabenz [a]anthracene 114J. 6,7-Diazabenz [a]anthracene 117K. 6,12-Diazabenz [a]anthracene 1203. Triazabenz [a]anthraccnes 121A. 4,7,12-Triazabenz[a]anthracene 121B. 6,7,12-Triazabenz[a]anthracene 1224. Tetrazabenzjajanthracenes 123A. 7,8,10,12-Tetrazabenz [a]anthracene 124B. 7,9,11,12-Tetrazabenz [a]anthracene 1245. Pentazabenz [a Janthraccnes 127A. 4,7,9,11,12-Pentazabenz[a]anthracene 127B. 4,7,8,10,12-Pentazabenz[a]anthracene 127III. Azabenzojc Jphenanthrenes 133By Eleanor K. Webster1. Monoazabenzo [c]phenanthrenes 133A. 1-Azabenzo[c]phenanthrenc 133B. 2-Azabenzo[c]phenanthrenc 134C. 4-Azabenzo[c]phenanthrenc 134D. 6-Azabenzo[c]phenanthrenc 1392. Diazabenzo[c]phenanthrenes 141A. 1,3-Diazabenzo[c]phenanthrcne 141B. 5,8-Diazabenzo[c]phenanthrenc 142IV. Azachrysenes 151By Jean V. Crawford1. Monoazachrysenes 151A. 1-Azachrysene 151B. 2-Azachrysene 154C. 3-Azachrysene 154D. 4-Azachrysene 155E. 5-Azachrysene 157(1) Chelidonine 160(2) Sanguinarine 166(3) α-Homochelidoninc 168(4) Chelerythrine 169F. 6-Azachrysene 1742. Diazachrysenes 174A. 1,10-Diazachrysene 174B. 2,4-Diazachrysene 175C. 4,10-Diazachrysenc 175V. Azatriphenylenes 185By Jean K Crawford1. Monoazatriphcnylcncs 185A. 1-Azatriphenylene 185B. 2-Azatriphenylene 1862. Diazatriphenylenes 188A. 1,2-Diazatriphenylene 188B. 1,4-Diazatri phenylene 188C. 1,8-Diazatriphenylene 191D. 2,3-Diazatriphcnylene 1923. Triazatriphenylenes 192A. 1,2,4-Triazatriphenylene 193B. 1,5,9-TriazatriphenyIene 198VI. Azabensanthrenes 201By C. F. H. Allen, D. M. Burners, and F. W. SpanglerIntroduction 201A. Historical 201B. Nomenclature 202(1) Numbering 202(2) 3-Azabenzanthrones (Anthrapyridines, Anthrapyridones) 202(3) 1,3-Diazabenzanthrones (Anthrapyrimidines) 2031. Monoazabenzanthrenes 204A. 7H,1-Azabenzanthrene 204By D. M. Burners(1) Preparation 204(2) Reactions 205(3) Properties 205B. 2-Azabenzanthrenes 207By D. M. Burners 207(1) Preparation 207(2) Reactions 208(3) Properties 209C. 3-Azabenzanthrenes 209By C. F. H. Allen(1) Monoketo Derivatives: 3-Azabenzanthroncs (Anthrapyridines) 209(2) Diketo Derivatives: 2-Keto-3-azabenzanthrones (Anthrapyridines) 213(a) Ring Closure, from 1-Aminoanthraquinone 214(b) Ring Closure. Seka’s Method 216(c) Formation of Substituted 2-Keto-3-azabenzanthrones 217(1) In the 1-Position 217(2) In the 3-Position 219(3) In the 4-Position 219(4) In the 6-Position 219(5) In the 8- and 11-Positions 220(6) Miscellaneous 221(d) Products of Uncertain Structures 222(e) “Dianthrapyridones” 223(3) Color 223D. 5-Azabenzanthrenes 228By D. M. Burness 228E. 6-Azabenzanthrenes 228By D. M. Burness 228(1) Introduction 229(2) Historical 229(3) Nomenclature 230(4) Stereochemistry 231(5) Preparation 231(6) Reactions 235(7) Properties 237(8) Source, Properties, and Physiological Action of the Natural Alkaloids 238(a) Apomorphine 238(b) Apocodeine 239(c) Roemerine 239(d) Anolobine 239(e) Morphothebaine 239(f) Tuduranine 240(g) Isothebaine 240(h) Pukateine 240(i) Laureline 241(j) Laurotetanine 241(k) Actinodaphnine 241(l) Boldine 242(m) Corytuberine 242(n) Laurepukine 243(o) N-Methyllaurotetanine 243(p) d-Corydine 243(q) Isocorydine 244(r) Domesticine 244(s) Isodomesticine 244(t) Bulbocapnine 245(u) Glaucine 245(v) Epidicentrine 246(w) Dicentrine 246(x) Glaucidine 246F. 7H,8-Azabenzanthrene 254By D. M. BurnessG. 7H,11-Azabenzanthrene 254By D. M. Burness(1) Preparation 254(2) Reactions 256(3) Properties 257H. x-Azabenzanthrenes 257By D. M. Burness2. Diazabenzanthrenes 260A. 1,2-Diazabenzanthrones (Pyridazinoanthrones) 260By F. W. Spangler(1) Historical 261(2) 3-Substituted 1,2-Diazabenz an thrones 262(a) Preparation 262(b) Properties 262(c) Uses 263(3) 3-Keto-1,2-diazabcnzanthrones 263(a) Preparation 263(b) Properties 265(c) Uses 265B. 1,3-Diazabenzanthrones 267By C. F. H. Allen(1) Monoketo-1,3-diazabenzanthrenes (Anthrapyrimidines) 267(a) Ring Closure 267(b) Replacement Reactions 272(1) Amines 27212) Halogenated Derivatives 273(3) Sulfonic Adds 273(4) Hydroxy Derivatives 274(5) Miscellaneous Derivatives 274(a) Acylamino-1,3-diazabenzanthrones 274(b) Arylamino-1,3-diazabenzanthrones 275(c) Haloamino-1,3-diazabenzanthrones 275(d) N-Alkylsulfonic Acids 275(e) Nitriles 275(f) Carboxylic Adds 276(g) Oxy, Thio, and Seleno Derivatives 276(2) Diketo-1,3-diazabenzanthrenes (Anthrapyrimidones) 277(3) Products of Uncertain Structure 279(4) Physical Properties 280(5) Uses 281VII. Azapyrenes 295By Eleanor R. Webster1. Monoazapyrenes 295A. 2-Azapyrene 295B. 4-Azapyrene 2962. Diazapyrenes 298A. 2,7-Diazapyrene 298B. 4,9-Diazapyrene 3023. Tetrazapyrenes 3051,3,6,8-Tetrazapyrene 305Azsbenzanthrenes: Addendum 311By C. P. Wilson1. 2-Keto-3-methyl-3-azabenzanthrones 3112. 1,3-Diazabenzanthrones 312A. Aryl Group in the 4-Position 312B. Sulfobenzoylation 312Index 315