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[null,"1.","Record Nr.",null,"UNINA9911019129903321"]
[null,null,"Autore",null,"Allen C. F. H (Charles Francis Hitchcock), <1895-1979.>"]
[null,null,"Titolo",null,"Six-membered heterocyclic nitrogen compounds with three condensed rings / / C.F.H. Allen ; in collaboration with G.M. Badger ... [et al.]"]
[null,null,"Pubbl/distr/stampa",null,"New York, : Interscience, 1958"]
[null,null,"ISBN",null,"9786612301469"]
[{"$nulls":4},"9781282301467"]
[{"$nulls":4},"1282301462"]
[{"$nulls":4},"9780470186619"]
[{"$nulls":4},"0470186615"]
[{"$nulls":4},"9780470188118"]
[{"$nulls":4},"0470188111"]
[null,null,"Descrizione fisica",null,"1 online resource (650 p.)"]
[null,null,"Collana",null,"Chemistry of heterocyclic compounds ; ; v. 12"]
[null,null,"Disciplina",null,"547.593"]
[{"$nulls":4},"547/.59/05"]
[null,null,"Soggetti",null,"Heterocyclic compounds"]
[{"$nulls":4},"Nitrogen compounds"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS A SERIES OF MONOGRAPHS; Preface; Contents; Introduction; Mechanism of Ring Closure; I. Azaanthracenes; 1. Monoazaanthracenes; A . 1-Azaanthracene; (1) Nomenclature; (2) Synthesis of 1-Azaanthracene; (a) From 6-Aminotetralin; (b) From 1-Azaanthraquinone; (c) From 9-Chloro-1-azaanthracene; (d) From 0-Xylyl Chloride and Pyridine; (e) From 2,4-Dicarboxy- 1-azaanthracene; Proof of Structure; (3) Substituted 1-Azaanthracenes; (a) By Ring Closure; Combes Synthesis; Skraup Synthesis; Doebner-Miller Synthesis; Conrad-Limpach Synthesis; Knorr Synthesis"]
[{"$nulls":4},"(6) 1-Azaanthraquinone and Its Derivatives(a) By Ring Closure; (b) By Oxidation of 1-Azaanthracene Derivatives; (c) By Direct Substitution in 1-Azaanthraquinone or Its Derivatives; (1) Halogenation; (2) Nitration; (3) Sulfonation; (d) By Replacement or Alteration of Other Groups; (1) Halogen Derivatives; (2) Hydroxy and Methoxy Derivatives; (3) Amino Derivatives; (e) Phomazarin; B. 2-Azaanthracene; (1) Nomenclature; (2) Syntheses of 2-Azaanthracenes; (a) 2-Azaanthracene; (b) 7-Methyl-2-azaanthracene; (c) 1-Benzyl-2-azaanthracene; (d) 9,l0-Diphenyl- 2-"]
[{"$nulls":4},"azaanthracene"]
[{"$nulls":4},"(3) Syntheses of 2-Azaanthraquinones(a) 2-Azaanthraquinone; (b) 5,8-Dihydroxy- 2-azaanthraquinone; (4) Properties of 2-Azaanthracenes; 2. Diazaanthracenes; A. 1,2-Diazaanthracene; (1) Nomenclature; (2)Syntheses; B. 1,3-Diazaanthracene; (1) Nomenclature; (2) Syntheses; (a) By Cyclization Procedures; (b) By Replacement of Other Groups; (3) 1,3-Diazaanthraquinones; C. 1,4-Diazaanthracene; (1) Nomenclature; (2) Synthesis; D. 1, 5-Diazaanthracene; (1) Nomenclature; (2) Syntheses; (a) 1, 5-Diazaanthracene; (b) 10-Methyl- 1, 5-diazaanthracene; (c) 2,6-Dimethyl-1, 5-diazaanthracene"]
[{"$nulls":4},"(d) 2,6-Dipheny 1. 1. 5.diazaanthraceneE. 1,8-Diazaanthracene; (1) Nomenclature; (2) Syntheses; F. 1,9-Diazaanthracene; (1) Nomenclature; (2) Historical; (3) Syntheses; G. 1,10-Diazaanthracene; (1) Nomenclature; (2) Syntheses; H. 2.3-Diazaanthracene; (1) Nomenclature; (2) Syntheses; I. 2,6-Diazaanthracene; J. 2,9-Diazaanthracene; K. 2,10-Diazaanthracene; (1) Nomenclature; (2) Syntheses; 3. Triazaanthracenes; Nomenclature; A . 1,2,3-Triazaanthracene; B. 1,2,4-Triazaanthracene; C. 1,3,9-Triazaanthracene; D. 1,8,9-Triazaanthracene; E. 1,9,10-Triazaanthracene; F. 2,3,9-Triazaanthracene"]
[{"$nulls":4},"G. 2,9,10-Triazaanthracene"]
[null,null,null,"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."]