Affiliation:
1. Department of Chemistry, Mewar University
2. Department of Pharmacy, Mewar University
Abstract
A convenient synthesis of 1,5-fused 1,2,4-triazoles from readily available N-arylamidines is reported. The reaction is efficiently promoted by chloramine-T to afford the desired products mostly in high yields and in relatively short time, through direct metal-free oxidative N−N bond formation. The mild nature of the synthesis and short reaction time are notable advantages of the developed protocol. This protocol is effective toward various substrates having different functionalities.
Subject
Organic Chemistry,Catalysis
Cited by
5 articles.
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