ANODIC BEHAVIOR OF AROMATIC OXIMES - AN ELECTROCHEMICAL DEOXIMATION REACTION

Citation
L. Bencharif et al., ANODIC BEHAVIOR OF AROMATIC OXIMES - AN ELECTROCHEMICAL DEOXIMATION REACTION, Electrochimica acta, 42(23-24), 1997, pp. 3509-3512
Citations number
18
Categorie Soggetti
Electrochemistry
Journal title
ISSN journal
00134686
Volume
42
Issue
23-24
Year of publication
1997
Pages
3509 - 3512
Database
ISI
SICI code
0013-4686(1997)42:23-24<3509:ABOAO->2.0.ZU;2-E
Abstract
Acetophenone oximes can be converted in high yield into the correspond ing ketones by controlled potential oxidation in wet acetonitrile. Whe reas, on the contrary, oxidation of benzaldoximes is not selective and leads to mixtures of aldehydes and benzoic acids, together with subst ituted 1,2,4-oxadiazoles. (C) 1997 Elsevier Science Ltd.