A highly convergent approach to O- and N-linked glycopeptide analogues

Glycoconj J. 1999 Aug;16(8):399-404. doi: 10.1023/a:1007026527040.

Abstract

Deprotected C-glycopyranosyl-ketones have been conjugated by a chemoselective approach to a peptide or an amino acid bearing an aminooxy group on the N-terminus or on the side-chain, respectively. The coupling reaction, performed in aqueous media, does not require protecting groups on the peptide or saccharide moieties, nor auxiliary coupling reagents.

MeSH terms

  • Amino Acid Sequence
  • Glycopeptides / chemistry*
  • Molecular Sequence Data
  • Protein Conformation

Substances

  • Glycopeptides