ortho-Methylphenylthioglycosides as glycosyl building blocks for preactivation-based oligosaccharide synthesis

Carbohydr Res. 2014 Jan 30:384:1-8. doi: 10.1016/j.carres.2013.11.009. Epub 2013 Nov 22.

Abstract

Thioglycosides are widely used in orthogonal glycosylation, armed-disarmed chemoselective glycosylation, and preactivation-based glycosylation. Nevertheless, aglycon transfer occasionally occurred in the glycosylation process of thioglycosides. This problem was also encountered in preactivation-based reactions, which limited the applications of preactivation-based glycosylation to some extent. To tackle this problem, sterically hindered aglycon ortho-methylphenylthioglycosides were introduced as glycosyl building blocks. These thioglycosides prevented the aglycon transfer and enhanced the efficiency of glycosyl coupling reactions, especially in the reactions of disarmed donors with armed acceptors. Moreover, these thioglycosides were employed in preactivation-based one-pot oligosaccharide assembly.

Keywords: Aglycon transfer; Glycosylation; Oligosaccharide; Preactivation; o-Methylphenylthioglycoside.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Molecular Structure
  • Oligosaccharides / chemical synthesis*
  • Oligosaccharides / chemistry*
  • Thioglycosides / chemistry*
  • Toluene / analogs & derivatives*
  • Toluene / chemistry

Substances

  • Oligosaccharides
  • Thioglycosides
  • Toluene