Affiliation:
1. School of Chemistry College of Science University of Tehran PO Box 14155-6455 Tehran Iran
2. Endocrinology and Metabolism Research Center Endocrinology and Metabolism Clinical Sciences Institute Tehran University of Medical Sciences Tehran Iran
Abstract
AbstractA library of pyrazino[1,2‐a]indoles has been synthesized via direct amidation and alkyne hydroamination reactions of the molecule produced by indole‐2‐carboxylic acid and propargyl bromide. The noteworthy features of the present strategy are short reaction time, excellent yields and a broad substrate scope. This cascade reaction also occurred under transition metal‐free and ambient conditions as well as operational simplicity.
Cited by
1 articles.
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