Bi3+ CATALYZED REGIOSELECTIVE RING OPENING OF EPOXIDES WITH AROMATIC AMINES

Epoxides undergo the facile ring opening with anilines to afford the corresponding β-amino alcohols in excellent yields by bismuth trichloride in acetonitrile at ambient temperature.

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Bibliographic Details
Published in:Synthetic communications 2002-01, Vol.32 (15), p.2307-2312
Main Authors: Raghavendra Swamy, N., Kondaji, G., Nagaiah, K.
Format: Article
Language:English
Online Access:Get full text
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Description
Summary:Epoxides undergo the facile ring opening with anilines to afford the corresponding β-amino alcohols in excellent yields by bismuth trichloride in acetonitrile at ambient temperature.
ISSN:0039-7911
1532-2432
DOI:10.1081/SCC-120006000