Synthesis of alpha-GalNAc thioconjugates from an alpha-GalNAc mercaptan

J Org Chem. 2002 May 3;67(9):2995-9. doi: 10.1021/jo0110909.

Abstract

A variety of functionalized thioglycosides and other derivatives (10-24) of 2-acetamido-2-deoxy-1-thio-alpha-D-galactopyranose have been prepared in good yields and with high anomeric purities by S-substitution reactions of the sulfide anion or sulfur-centered radical from mercaptan 6. Given the importance in nature of the alpha-GalNAc 1-O-linkage, and the greater chemical and biological stability of the corresponding 1-S-linkage, these thioconjugates may find application in studies of synthetic vaccines, enzyme inhibitors, glycomimetic scaffolds, and other complex carbohydrate systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry
  • Alkylation
  • Antigens, Tumor-Associated, Carbohydrate
  • Catalysis
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Oxidation-Reduction
  • Sulfhydryl Compounds / chemical synthesis
  • Thiogalactosides / chemical synthesis*
  • Thiogalactosides / chemistry*

Substances

  • 2-acetamido-2-deoxy-1-thio-alpha-D-galactopyranose
  • 2-acetamido-2-deoxy-2,3,4-tri-O-acetyl-1-thio-alpha-D-galactopyranose
  • Alkenes
  • Antigens, Tumor-Associated, Carbohydrate
  • Sulfhydryl Compounds
  • Thiogalactosides
  • Tn antigen