Iodine-catalyzed stereoselective synthesis of allylglycosides, glycosyl cyanides and glycosyl azides

Yadav, J. S. ; Reddy, B. V. S. ; Venkateshwar Rao, C. ; Chand, Pratap. K. ; Prasad, A. R. (2001) Iodine-catalyzed stereoselective synthesis of allylglycosides, glycosyl cyanides and glycosyl azides Synlett, 2001 (10). pp. 1638-1640. 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-2001-17438

Abstract

Iodine efficiently catalyzes the glycosidation of glycals with allyltrimethylsilane, trimethylsilyl cyanide and trimethylsilyl azide in dichloromethane at ambient temperature to afford the corresponding 2,3-unsaturated allyl glycosides, glycosyl cyanides and glycosyl azides in excellent yields with high α-selectivity.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Ferrier Rearrangement; Glycals; Iodine; C-glycosides
ID Code:62781
Deposited On:24 Sep 2011 04:35
Last Modified:24 Sep 2011 04:35

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