Stereoselective Synthesis of 2-Deoxythiosugars from Glycals

Molecules. 2022 Nov 17;27(22):7979. doi: 10.3390/molecules27227979.

Abstract

2-deoxythiosugars are more stable than 2-deoxysugars occurring broadly in bioactive natural products and pharmaceutical agents. An effective and direct methodology to stereoselectively synthesize α-2-deoxythioglycosides catalyzed by AgOTf has been developed. Various alkyl thiols and thiophenols were explored and the desired products were formed in good yields with excellent α-selectivity. This method was further applied to the syntheses of S-linked disaccharides and late-stage 2-deoxyglycosylation of estrogen, L-menthol, and zingerone thiols successfully.

Keywords: 2-deoxythioglycosides; glycals; glycosylation; silver triflate; stereoselective synthesis.

MeSH terms

  • Catalysis
  • Glycosides*
  • Glycosylation
  • Stereoisomerism
  • Sulfhydryl Compounds*

Substances

  • Glycosides
  • Sulfhydryl Compounds