Unexpected orthogonality of S-benzoxazolyl and S-thiazolinyl glycosides: application to expeditious oligosaccharide assembly

Org Lett. 2009 Feb 19;11(4):799-802. doi: 10.1021/ol802740b.

Abstract

Thorough mechanistic studies of the alkylation pathway for the activation of glycosyl thioimidates have led to the development of the "thioimidate-only orthogonal strategy". Discrimination among S-thiazolinyl (STaz) and S-benzoxazolyl (SBox) anomeric leaving groups was achieved by fine-tuning of the activation conditions. Preferential glycosidation of a certain thioimidate is not simply determined by the strength of activating reagents; instead, the type of activation--direct vs indirect--comes to the fore and plays the key role.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alkylation
  • Animals
  • Benzoxazoles / chemistry*
  • Glycosides / chemistry*
  • Glycosylation
  • Imidoesters / chemistry
  • Molecular Structure
  • Oligosaccharides / chemical synthesis*
  • Oligosaccharides / chemistry
  • Thiazoles / chemistry*

Substances

  • Benzoxazoles
  • Glycosides
  • Imidoesters
  • Oligosaccharides
  • Thiazoles