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Turkish Journal of Chemistry

DOI

10.3906/kim-1212-26

Abstract

A series of novel N-[3-(2-benzo[d]thiazol-2-yl)-4-methylthiazol-2(3H)-ylidene] substituted benzamides (2a--k) were efficiently synthesized by heterocyclization of the corresponding 1-(benzo[d]thiazol-2-yl)-3-aroylthioureas (1a--k). The cyclization was achieved by the reaction of \alpha-bromoacteone produced in situ using bromine in dry acetone in the presence of triethylamine.

First Page

909

Last Page

916

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