1.

Record Nr.

UNINA9910830532103321

Autore

Allen C. F. H (Charles Francis Hitchcock), <1895-1979.>

Titolo

Six-membered heterocyclic nitrogen compounds with four condensed rings [[electronic resource] /] / C.F.H. Allen ; in collaboration with D.M. Burness ... [et al.]

Pubbl/distr/stampa

New York, : Interscience, 1951

ISBN

1-282-30136-5

9786612301360

0-470-18651-8

0-470-18801-4

Descrizione fisica

1 online resource (362 p.)

Collana

Chemistry of heterocyclic compounds ; ; v. 2

Disciplina

547.593

547/.59/05

Soggetti

Heterocyclic compounds

Nitrogen compounds

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Description based upon print version of record.

Nota di bibliografia

Includes bibliographical references and index.

Nota di contenuto

SIX-MEMBERED HETEROCYCLIC NITROGEN COMPOUNDS WITH FOUR CONDENSED RINGS; Preface; Contents; Introduction; I. Azanaphthacenes; 1. Monoazanaphthacenes; A. 1-Azanaphthacene; B. 2-Azanaphthacene; C. 5-Azanaphthacene; 2. Diazanaphthacenes; A. 1,3-Diazanaphthacene; B. 1,4-Diazanaphthacene; C. 1, 11-Diazanaphthacene; D. 2,3-Diazanaphthacene; E. 5,6-Diazanaphthacenc; F. 5,11-Diazanaphthacene; G. 5,12-Diazanaphthacene; 3. Triazanaphthacenes; A. 1,6,11-Triazanaphthacene; B. 5,6, 11 -Triazanaphthacene; 4. Tetrazanaphthacenesl; A. 1,3,5,12-Tetrazanaphthacene; B. 1,4,6, 11-Tetrazanaphthacene

C. 5,6,11,12-TetrazanaphthaceneII. Azabenz[a]anthracenes; 1. Monoazabenz[a]anthracenes; A. l-Azabenz[a]anthracene; B. 4-Azabenz[a]anthracene; (1) Alkyl Derivatives; (2) Oxidation Products; (3) Halogen Derivatives; (4) Nitro Derivatives; (5) Sulfonated and Hydroxylated Derivatives; (6) Physical Properties; (7) Amino Compounds; C. 5-Azabenz[a]anthracene; D. 8-Azabenz [a] anthracene; E. 10-Azabenz[a]



anthracene; F. 11-Azabcnz[a]anthraccne; 2. Diazabenz[c]anthracenes; A. 1,3-Diazabenz[a]anthracene; B. 1,4-Diazabenz[a]anthracene; C. 1, 7-Diazabenz [a] anthracene; D. 1,12-Diazabenz[a]anthracene

E. 2,4-Diazabenz[a]anthraceneF. 4,7-Diazabenz[a]anthracene; G. 4,12-Diazabenz[a]anthracene; H. 5,7-Diazabenz[a]anthracene; (1) Ciba Yellow 3G; (2) Höchst Yellow U; (3) Höchst Yellow R; I. 5,12-Diazabenz[a]anthracene; J. 6,7-Diazabenz[a]anthracene; K. 6,12-Diazabenz[a]anthracene; 3. Triazabenz[a]anthracenes; A. 4,7,12-Triazabenz[a]anthracene; B. 6,7,12-Triazabenz[a]anthracene; 4. Tetrazabenz [a]anthracenes; A. 7,8,10,12-Tetrazabenz[a)anthracene; B. 7,9,11,12-Tctrazabenz[o]anthracene; 5. Pentatabenz[a]anthracenes; A. 4,7,9,11,12-Pentazabenz[o]anthracene; B. 4,7,8,10, 12-Pentazabenz[a]anthracene

III. Azabenzo[c]phenanthrenes1. Monoazabenzo[c]phenanthrenes; A. l-Azabenzo[c]phenanthrene; B. 2-Azabenzo[c]phenanthrene; C. 4-Azabenzo[c]phenanthrene; D. 6-Azabenzo[c]phenanthrene; 2. Diazabenzo[c]phenanthrenes; A. 1, 3-Diazabenzo[c]phenanthrene; B. 5,8.Diazabenzo[c]phenanthrenes; IV. Azachrysencr; 1. Monoazachrysenes; A. 1-Azachrysene; B. 2-Azachrysene; C. 3-Azachrysene; D. 4-Azachrysene; E. 5-Azachrysene; (1) Chelidonine; (2) Sanguinarine; (3) α-Homochelidonine; (4) Chelerythrine; F. 6-Azachrysene; 2. Diazachrysenes; A. 1,10-Diazachrysene; B. 2.4-Diazachrysene; C. 4.10-Diazachrysene

V. Azartriphenylenes1. Monoazatriphenylenes; A. 1-Azatriphenylene; B. 2-Azatriphenylene; 2. Diazatriphenylenes; A. 1,2-Diazatriphenylene; B. 1, 4-Diazatriphenylene; C. 1; 8-Diazatriphenylene; D. 2,3-Diazatriphenylene; 3. Triazatriphenylenes; A. 1,2,4-Triazatriphenylene; B. 1,5,9-Triazatriphenylene; VI. Azabenzanthrenes; Introduction; A. Historical; B. Nomenclature; (1) Numbering; (2) 3-Azabenzanthrones (Anthrapyridines, Anthrapyridones); (3) 1, 3-Diazabenzanthrones (Anthrapyrimidines); 1. Monoazabenzanthrenes; A. 7H,1-Azabenzanthrene; (1) Preparation; (2) Reactions; (3) Properties

B. 2-Azabenzanthrenes

Sommario/riassunto

Chemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus.