1.

Record Nr.

UNISA996202935303316

Autore

Swan G. A (George Albert), <1917->

Titolo

Phenazines [[electronic resource] /] / G.A. Swan, G.G.I. Felton

Pubbl/distr/stampa

New York, : Interscience, 1957

ISBN

1-282-30145-4

9786612301452

0-470-18660-7

0-470-18810-3

Descrizione fisica

1 online resource (718 p.)

Collana

Chemistry of heterocyclic compounds ; ; v. 11

Altri autori (Persone)

FeltonD. G. I (Desmond Geoffrey Ivins)

Disciplina

547

547.615

547/.59/05

Soggetti

Phenazine

Chemistry

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

PHENAZINES; Preface; Contents; Part I.  Phenazine Systems Not Carrying Condensed Rings; I. General Methods for the Synthesis of Phenazine. Its Homologs and Derivatives Not Containing Condensed Nuclei; References; II. Phenazine and Its Homologs; 1. Phenazine; A. Physical Constants; B. Preparation and Importance; C. Structure; D. Salts and Addition Compounds; E. Phenazine-5-oxide; F. Phenazine-5,10-dioxide; 2. Phenazinium Compounds; A. Structure; B. 5-Methylphenazinium Methyl Sulfate; C. 5-Ethylphenazinium Ethyl Sulfate; D. 5-Phenylphenazinium Compounds; 3. Homologs of Phenazine; References

III. Hydrogenated Derivatives of Phenazine1.Dihydrophenazines; A. 5,10-Dihydrophenazine; B. 5,10-Dihydro-5-methylphenazine; C. 5-Ethyl-5,l0-dihydrophenazine; D. 5,10-Dihydro-5,10-dimethylphenazine; E. 5,10-Dihydro-5-phenylphenazine; F. 5,l0-Diaryl-5,10-dihydrophenazines (Perazines); 2. The Phenazhydrins, Phenazyls and Semiquinones; A. Historical; B. Semiquinones of the Phenazine Series; C. The Phenazyls; D. The Phenazhydrins; E. Complexes Formed between Phenazine and Primary or Secondary



Aromatic Bases; F. Complex Salts of the Phenazhydrins; G. Conclusion; 3. Tetrahydrophenazines

A . 1,2,3,4-TetrahydrophenazineB. 1,2,3,4-Tetrahydro-1-methylphenazine; C. 1,2,3,4-Tetrahydro-2-methylphenazine; D. 1,2,3,4-Tetrahydro-7-methylphenazine; E. 2,3,5,10-Tetrahydro-5,10-dimethylphenazine; 4. Octahydrophenazines; A. 1,2,3,4,6,7,8,9-Octahydrophenazine; B. cis-and trans-1,2,3,4,4a,5,10,10a-Octahydrophenazines; 5.Tetradecahydrophenazines; 6. Hydrophenazines Derived from Camphor, etc.; A. Introduction .; B. 1,2,3,4,4a,6,7,8,9,9a-Decahydro-1,6,11,11,12,12-hexamethyl-1,4,6,9-dimethanophenazine; C. 1,2,3,4,6,7,8,9-Octahydro-1,6,11,11,12,12-hexamethyl-l,4,6,9-dimethanophenazine

D. 1,2,3,4,4a,5,5a,6,7,8,9,9a,10,10a,Tetradecahydro-1,6,11,12,12-hexamethyl-1,4,6,9-dimethanophenazineE. 1,2,3,4.5a,6,7,8,9.10a-Decahydro-1,6,11,11,12,1,2-hexamethyl-1,4,6,9-dimethanophenazine; F. 1,2,3,4,6,7,8,9-Octahydro-1,9,11,11,12,12,hexamethyl-l,4,6,9-dimethanophenazine; G. 1,2,3,4,4a,6,7,8,9,9a-Decahydro-1,9,11,11,12,12-hexamethyl-1,4,6,9-dimethanophenazine; H. 1,2,3,4,4a.5,6,7,8,9,10,10a-Dodecahydro-1,9,11,11,12,1 2-hexamethyl-1,4,6,9-dimethanophenazine; I. Other Related Compounds; References; IV. Substitution Products of Phenazine (Excluding Hydroxy and Amino Compounds)

1. Introduction2.  Halogen Derivatives; 3. Nitro Derivatives; 4. Sulfones; 5. Sulfonic Acids; 6. Phenazinecarboxylic Acids; A. 1-Phenazinecarboxylic Acid; B. 2-Phenazinecarboxylic Acid; C. Phenazinedicarboxylic Acids; 7. Sirius Light Yellow R . R; 8. Arsonic Acids; References; V. Hydroxy and Keto Derivatives of Phenazine; 1. Introduction; 2. Monohydroxy and Monoketo Derivatives; A. 1-Phenazinol; B. 2-Phenazinol; C. Aposafranone; D. 3-Hydroxy-10-phenylphenazinium Salts; 3. Derivatives Containing Two Oxygen Atoms; A. Phenazinediols; B. 3-Hydroxyaposafranone; C. Phenosafranol

4. Derivatives Containing Three or More Oxygen Atoms

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.