LEADER 05357nam 2200733Ia 450 001 9911019862203321 005 20200520144314.0 010 $a9786612301452 010 $a9781282301450 010 $a1282301454 010 $a9780470186602 010 $a0470186607 010 $a9780470188101 010 $a0470188103 035 $a(CKB)1000000000376519 035 $a(EBL)469947 035 $a(OCoLC)729013552 035 $a(SSID)ssj0000364290 035 $a(PQKBManifestationID)11254776 035 $a(PQKBTitleCode)TC0000364290 035 $a(PQKBWorkID)10395594 035 $a(PQKB)10719433 035 $a(MiAaPQ)EBC469947 035 $a(PPN)240648730 035 $a(Perlego)2766057 035 $a(EXLCZ)991000000000376519 100 $a20070725d1957 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aPhenazines /$fG.A. Swan, G.G.I. Felton 210 $aNew York $cInterscience$d1957 215 $a1 online resource (718 p.) 225 1 $aChemistry of heterocyclic compounds ;$vv. 11 300 $aDescription based upon print version of record. 311 08$a9780470182741 311 08$a0470182741 320 $aIncludes bibliographical references and index. 327 $aPHENAZINES; 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 327 $aIII. 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 327 $aA . 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 327 $aD. 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) 327 $a1. 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 327 $a4. Derivatives Containing Three or More Oxygen Atoms 330 $aChemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. 410 0$aChemistry of heterocyclic compounds ;$vv. 11. 606 $aPhenazine 606 $aChemistry 615 0$aPhenazine. 615 0$aChemistry. 676 $a547 676 $a547.615 676 $a547/.59/05 700 $aSwan$b G. A$g(George Albert),$f1917-$0856097 701 $aFelton$b D. G. I$g(Desmond Geoffrey Ivins)$0856098 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911019862203321 996 $aPhenazines$91911308 997 $aUNINA