Ring opening of epoxides and aziridines with sodium azide using Oxone® in aqueous acetonitrile: a highly regioselective azidolysis reaction

Sabitha, Gowravaram ; Satheesh Babu, R. ; Shashi Kumar Reddy, M. ; Yadav, J. S. (2002) Ring opening of epoxides and aziridines with sodium azide using Oxone® in aqueous acetonitrile: a highly regioselective azidolysis reaction Synthesis, 2002 (15). pp. 2254-2258. ISSN 0039-7881

Full text not available from this repository.

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

Related URL: http://dx.doi.org/10.1055/s-2002-34848

Abstract

A wide variety of epoxides and aziridines were converted to the corresponding β-azido alcohols and β-azido amines with sodium azide using Oxone® in aqueous acetonitrile. The reactions were highly regioselective and efficient with excellent yields at room temperature under mild reaction conditions.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Oxone®; Epoxides; Aziridines; Azides; Regioselectivity
ID Code:62928
Deposited On:24 Sep 2011 04:39
Last Modified:24 Sep 2011 04:39

Repository Staff Only: item control page