ELECTROCHEMISTRY OF 7-CARBOETHOXYCYCLOHEPTATRIENE AND ITS AZA-ANALOGS- RING CONSTRUCTION OF AZEPINE DERIVATIVES TO ANILINE DERIVATIVES BY OXIDATION AND N-N BOND RUPTURE OF DIAZEPINE DERIVATIVES TO 1-AMINO-4-CYANO-1,3-BUTADIENE DERIVATIVES BY REDUCTION

Citation
S. Kondo et al., ELECTROCHEMISTRY OF 7-CARBOETHOXYCYCLOHEPTATRIENE AND ITS AZA-ANALOGS- RING CONSTRUCTION OF AZEPINE DERIVATIVES TO ANILINE DERIVATIVES BY OXIDATION AND N-N BOND RUPTURE OF DIAZEPINE DERIVATIVES TO 1-AMINO-4-CYANO-1,3-BUTADIENE DERIVATIVES BY REDUCTION, Heterocycles, 48(6), 1998, pp. 1151-1156
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
03855414
Volume
48
Issue
6
Year of publication
1998
Pages
1151 - 1156
Database
ISI
SICI code
0385-5414(1998)48:6<1151:EO7AIA>2.0.ZU;2-D
Abstract
Electrochemical reduction or oxidation of 7-ethoxycasbonylcycloheptatr iene afforded 2-ethoxycarbonylcycloheptatriene and ethyl phenylacetate , respectively. N-Alkoxycarbonyl-1H-azepine formed N-alkoxycarbonylani line in electrochemical oxidation vis a ring contruction. N-Alkoxycarb onyl-1H-1,2-diazepine afforded N-Alkoxycarbonyl-1-amino-4-cyano-1,3-bu tadiene in electrochemical reduction via an N-N bond fission.