Chemoselective ligation in glycochemistry

Chem Commun (Camb). 2004 Mar 21:(6):623-7. doi: 10.1039/b308907j. Epub 2003 Nov 14.

Abstract

This feature article describes chemoselective techniques for the assembly of neoglycopeptides and oligosaccharide mimics. Chemoselective ligation, allowing the use of aqueous environments and non-protected substrates, provides rapid access to complex glycoconjugates. The role of these molecules in recognition, signal transduction pathways and other events of fundamental biomedical significance is an object of study in the emerging field of chemical glycomics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Carbohydrate Sequence
  • Glycopeptides / chemical synthesis*
  • Glycosylation
  • Molecular Sequence Data
  • Molecular Structure
  • Oligosaccharides / chemical synthesis
  • Oligosaccharides / chemistry*
  • Peptides / chemistry*
  • Stereoisomerism
  • Water / chemistry

Substances

  • Glycopeptides
  • Oligosaccharides
  • Peptides
  • Water