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
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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 |
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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 |
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