OXIDATION OF 1-[(ARYL)(PHENYISELENO)METHYL]BENZOTRIAZOLE, ARYL)(ARYLTHIO)(PHENYLSELENO)METHYL]BENZOTRIAZOLE, AND 1-[(ARYL)(DIPHENYLSELENO)METHYL]BENZOTRIAZOLE WITH M-CHLOROPERBENZOIC ACID

Authors
Citation
Yh. Kang et K. Kim, OXIDATION OF 1-[(ARYL)(PHENYISELENO)METHYL]BENZOTRIAZOLE, ARYL)(ARYLTHIO)(PHENYLSELENO)METHYL]BENZOTRIAZOLE, AND 1-[(ARYL)(DIPHENYLSELENO)METHYL]BENZOTRIAZOLE WITH M-CHLOROPERBENZOIC ACID, Journal of heterocyclic chemistry, 34(6), 1997, pp. 1741-1752
Citations number
50
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0022-152X
Volume
34
Issue
6
Year of publication
1997
Pages
1741 - 1752
Database
ISI
SICI code
0022-152X(1997)34:6<1741:OO1A>2.0.ZU;2-5
Abstract
During the last decade, benzotriazole (1) has received much attention as an excellent synthetic auxiliary [1]. Recently Katritzky, et al. [2 ] studied the oxidation of 1-(phenylthiomethyl)benzotriazole (2a) and 1-(2-phenyl-1-phenylthioethyl)benzotriazole (2b) and obtained their su lfones and sulfoxides by treatment with m-chloroperbenzoic acid (m-CPB A) and sodium periodate, respectively. No compounds derived from a het erolytic cleavage between the alpha-carbon and the N-1 atoms of the fo regoing compounds were isolated.