Scandium triflate catalyzed Ferrier rearrangement: an efficient synthesis of 2,3-unsaturated glycopyranosides

Yadav, J. S. ; Subba Reddy, B. V. ; Murthy, C. V. S. R. ; Mahesh Kumar, G. (2000) Scandium triflate catalyzed Ferrier rearrangement: an efficient synthesis of 2,3-unsaturated glycopyranosides Synlett, 2000 (10). pp. 1450-1451. 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-2000-7632

Abstract

Scandium(III) trifluoromethanesulfonate is found to catalyze efficiently the O-glycosidation of 3,4,6-tri-O-acetyl-d-glucal with various alcohols and phenols to afford the corresponding 2,3-unsaturated glycosides in excellent yields with good anomeric selectivity.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Glucal; Scandium Triflate; Ferrier Rearrangement; Glycosides
ID Code:60453
Deposited On:09 Sep 2011 03:48
Last Modified:09 Sep 2011 03:48

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