Highly Direct alpha-Selective Glycosylations of 3,4-O-Carbonate-Protected 2-Deoxy- and 2,6-Dideoxythioglycosides by Preactivation Protocol

Org Lett. 2008 Aug 21;10(16):3445-8. doi: 10.1021/ol801190c. Epub 2008 Jul 17.

Abstract

A new efficient pre-activation method for the highly alpha-stereoselective glycosylation of 2-deoxysugars and 2,6-dideoxysugars has been developed using 2-deoxy- and 2,6-dideoxythioglycosides as glycosyl donors. The approach allows a wide range of glycosyl acceptors and donors to be used; the alpha-selectivity is very good to excellent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Conformation
  • Carbonates / chemistry*
  • Glycosylation
  • Stereoisomerism
  • Thioglycosides / chemical synthesis*
  • Thioglycosides / chemistry

Substances

  • Carbonates
  • Thioglycosides