Issue 7, 1991

Oxidative S-dealkylation of tert-butyl aryl sulphides: a novel route to 3-substituted-3H-1,2-benzodithioles

Abstract

Substituted 3H-1,2-benzodithioles are readily synthesized by an oxidative S-dealkylation reaction of mercapto tert-butyl sulphides 8 with N-bromosuccinimide in acetonitrile without prior deprotection of the tert-butyl group.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 540-541

Oxidative S-dealkylation of tert-butyl aryl sulphides: a novel route to 3-substituted-3H-1,2-benzodithioles

M. F. Chan and M. E. Garst, J. Chem. Soc., Chem. Commun., 1991, 540 DOI: 10.1039/C39910000540

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