Chemistry of Heterocyclic Compounds. Volume 2. Six-Membered Heterocyclic Nitrogen Compounds With Four Condensed Rings

دسته بندی: شیمی ارگانیک
ویرایش:  
نویسندگان: Allen C.F.H.  
سری:  
 
ناشر:  
سال نشر:  
تعداد صفحات: 352 
زبان: English 
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) 
حجم فایل: 7 مگابایت 

قیمت کتاب (تومان) : 51,000

Interscirnce Publishers, Inc., 1951. — 345 p. The Chemistry of Heterocyclic Compounds has been published since 1950 under the initial editorship of Arnold Weissberger, and later, until his death in 1984, under the joint editorship of Arnold Weissberger and Edward C. Taylor. In 1997, Peter Wipf joined Prof. Taylor as editor. This series attempts to make the extraordinarily complex and diverse field of heterocyclic chemistry as organized and readily accessible as possible. Each volume has traditionally dealt with syntheses, reactions, properties, structure, physical chemistry, and utility of compounds belonging to a specific ring system or class (e.g., pyridines, thiophenes, pyrimidines, threemembered ring systems). This series has become the basic reference collection for information on heterocyclic compounds. Contents Preface
Introduction Aznaphtacenes

Monoazanaphthacenes
1-Aznaphtacene
2-Aznaphtacene
5-Aznaphtacene
Diazanaphthacenes
1,3-Diazanaphthacene
1,4-Diazanaphthacene
1,1-Diazanaphthacene
2,3-Diazanaphthacene
5,6-Diazanaphthacene
5,11-Diazanaphthacene
5,12-Diazanaphthacene
Triazanaphthacenes
1,6,11-Triazanaphthacene
5,6,11-Triazanaphthacene
Tetrazanaphthacenes
1,3,5,12-Tetrazanaphthacene
5,6,11,
12.Tetrazanaphthacene
1,4,6,11-Tetrazanaphthacene Azabenz[a]anthracenes Monozabenz[a]anthracenes
1-Azabenz[a]anthracene
4-Azabenz[a]anthracene
Alkyl Derivatives
Oxidation Products
Halogen Derivatives
Nitro Derivatives
Sulfonated and Hydroxylated Derivatives
Physical Properties
Amino Compounds
5-Azabenz[a]anthracene
8-Azabenz[a]anthracene
10-Azabenz[a]anthracene
11-Azabenz[a]anthracene
Diazabenz[a]anthracenes
1,3-Diazabenz[alanthracene
1,4-Diazabenz[a]anthracene
1,7-Diazabenz[a]anthracene
1,12-Diazabenz[a]anthracene
2,4-Diazabenz[a]anthracene
4,7-Diazabenz[a]anthracene
4,12-Diazabenz[a]anthracene
5,7-Diazabenz[a]anthracene
Ciba Yellow 3C
Hochst Yellow U
Hochst Yellow R
5,12-Diazabenz[a]anthracene
6,7-Diazabenz[a]anthracene
6,12-Diazabenz[a]anthracene
Triazabenz[a]anthracenes
Tetrazabenz[a]anthracenes
Pentatabenz[a]anthracenes
4,7,12-Triazabenz[a]anthracene
6,7,12-Triazabenz[a]anthracene
7,8,10,12-Tetrazabenz[a]anthracene
7,9,11,12-Tetrazabenz[a]anthracene
4,7,9,11,12-Pentazabenz[a]anthracene
4,7,8,10,12-Pentazabenz[a]anthracene Azabenzo[c]phenanthrenes Monoazabenzo[c]phenanthrenes
1-Azabenzo[c]phenanthrene
2-Azabenzo[c]phenanthrene
4-Azabenzo[c]phenanthrene
6-Azabenzo[c]phenanthrene
Diazabenzo[c]phenanthrenes
1,3-Diazabenzo[c]phenanthrene
5,8-Diazabenzo[c]phenanthrene Azachrysenes Monoazachrysen
1-Azachrysene
2-Azachrysene
3-Azachrysene
5-Azachryscne
Chelidonine
Sanguinarine
a-Homochelidonine
Chelerythrine
6-Azachryscne
Diazachrysencs
4.10-Diazachrysene Azatriphenylenes Monoazatriphenylenes
1-Azatriphenylene
2-Azatriphenylene
Diazatriphenylenes
1,2-Diazatriphenylene
1,4-Diazatriphenylene
2,3-Diazatriphenylcne
1,8-Diazatriphenylene
2,3-Diazatriphenylene
Triazatriphenylencs
1,2,4-Triazatriphenylene
1,5,9-Triazatriphenylene Azabenzanthrenes Introduction
Historical
Nomenclature
Numbering
3-Azabenzanthrones (Anthrapyridines. Anthrapyridones)
1,3-Diazabcnzanthrones (Anthrapyrimidines)
Monoazabenzanthrenes
7H,1-Azabenzanthrene
Preparation
Reactions
Properties
2-Atabenzanthrene
Preparation
Reactions
Properties
3-Azabenzanthrenes
Monoketo Derivatives: 3-Azabenzanthrones (Anthrapyridines)
Diketo Derivatives: 2-Keto-3-azabenzanthrones (Anthrapyridons)
Ring Closure, from 1-Aminoanthraquinone
Ring Closure. Seka’s Method
In the 1-Position
Inthe 3-Pdtion
In the CPOeition
In the &Position
In the 8- and 11-Positions
Mtecllaneous
Formation of Substituted 2-Keto-3-azanthrones
Products of Uncertain Structures
Wianthrapyridones
5-Azabenzanthrenes
6-Azabenzanthrenes
Introduction
Histotical
Nomenclature
Stereochemistry
Prepatation
Reactions
Properties
Source,Properties and Physiological Action of the Natural Alkaloids
Apomorphine
Apocodeine
Morphothebaine
Tuduranine
Isothebaine
Laurcline
Laurotetanine
Actinodaphnine
Boldine
Corytuberine
Laurepukine
N-Methyllaurotetanine
d-Corydin
Isocorydine
Domesticine
Bulbocapnine
Glaucine
Epidicentrine
Dicentrine
7H,8-Azabenzanthrene
7H,11-Azabenzanthrene
Preparation
Reactions
Properties
x-Azabcnzanthrenes
Diazabenzanthrene
1,2-Diazabenzanthrones (Pyridazinoanthrones)
Historical
3-Subetituted 1,2-Diazabenzanthrones
Preparation
Properties
Uses
3-Keto-1,2-diazabenzanthrone
Preparation
Properties
Uses
Monoketo-1, 3-diazabenzanthrenes (Anthrapyrimidines)
Ring Closure
Replacement Reactions
Amines
Halogenated Derivatives
Sulfonic Acids
Hydroxy Derivatives
Miscellaneous Derivatives
Acylamino-1,3-diazabenzanthrones
Arylamino-1,3-diazabenzanthrones
Haloamino-1,3-diazabenzanthrones
N-Akylsulfonic Acids
Nitriles
Carboxylic Acids
Oxy, Thio, and Seleno Derivatives
Diketo-1,3-diazabenzanthrenes (Anthrapyrimidones)
Products of Uncertain Structure
Physical Properties
Uses Azapyrenes Monoazapyrenes
2-Azapyrene
4-Azapyrene
Diazapyrenes
2,7-Diazapyrene
4,9-Diazapyrene
Tetrazapyrene
1,3,6,8-Tetrazapyrene Azabenzanthrenes: Addendum 2-Keto-3-methyl-3-azabenzanthrones
1,3-Diazabenzanthrone
Aryl Group in the 4 Position
Sulfobenzoylation
Index