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Report | Regular issue | Vol 23, No. 10, 1985, pp.2583-2588
Published online, 1st January, 1970
DOI: 10.3987/R-1985-10-2583
■ Dihydrochalocones as Synthons for 2-Amino- and 2-Mercapto-4-aryl-5-arylmethylthiazoles

Vinod Kumar Ahluwalia,* Krishan Kumar Arora, and Gurvinder Kaur

*Department of Chemistry, University of Delhi, Delhi-110 007, India

Abstract

2-Amino- and 2-mercapto-4-aryl-5-arylmethylthiazoles have been synthesised by the respective condensation of thiourea and ammonium dithiocarbamate with α-bromo-α,β-dihydrochalcones which in turn are obtained by the bromination of the corresponding dihydrochalcones.