Indium trihalide mediated regioselective ring opening of aziridines: a facile synthesis of 2-haloamines

Yadav, J. S. ; Subba Reddy, B. V. ; Mahesh Kumar, G. (2001) Indium trihalide mediated regioselective ring opening of aziridines: a facile synthesis of 2-haloamines Synlett, 2001 (9). pp. 1417-1418. ISSN 0936-5214

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Official URL: http://www.thieme-connect.com/ejournals/abstract/s...

Related URL: http://dx.doi.org/10.1055/s-2001-16775

Abstract

A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambient temperature to afford the corresponding haloamines in excellent yields with high regioselectivity.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Aziridines; Indium Halides; Haloamines
ID Code:62962
Deposited On:24 Sep 2011 04:35
Last Modified:24 Sep 2011 04:35

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