Concise Synthesis of 1-Thioalkyl Glycoside Donors by Reaction of Per-O-acetylated Sugars with Sodium Alkanethiolates under Solvent-Free Conditions

J Org Chem. 2022 Mar 4;87(5):3638-3646. doi: 10.1021/acs.joc.1c02171. Epub 2022 Jan 21.

Abstract

A relatively green method for synthesizing 1-thioalkyl glycosides has been developed, where sodium alkanethiolates were used to react with per-O-acetylated sugars instead of odorous alkyl mercaptans in the presence of BF3·Et2O without the use of solvents under mild conditions. Furthermore, we found that 1,2-trans-β-thioglycosides can be converted into corresponding 1,2-cis-α-thioglycosides in the presence of trifluoromethanesulfonic acid in nonpolar solvents under mild conditions. This provides a simple and efficient new approach for synthesizing challenging 1,2-cis-α-thioglycosides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Glycosides*
  • Sodium
  • Solvents
  • Sugars
  • Thioglycosides*

Substances

  • Glycosides
  • Solvents
  • Sugars
  • Thioglycosides
  • Sodium