Development of glycosylation using the glucopyranose 1,2-orthobenzoate under electrochemical conditions

Org Lett. 2013 Nov 1;15(21):5484-7. doi: 10.1021/ol4026342. Epub 2013 Oct 9.

Abstract

Substituted glucopyranose 1,2-orthobenzoate undergoes β-selective glycosylation. The developed orthobenzoate derivative was stable under standard workup conditions and efficiently provided a variety of glycosides by EGA (electrogenerated acid), produced by anodic oxidation of cyclohexanol. Upon comparison with Lewis and Brønsted acids, EGA superiorly affected activation of the orthoester to afford desired glycosides possessing such aglycons as sugars, steroids, and adamantanes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzoates / chemistry*
  • Glycosides / chemistry*
  • Glycosylation
  • Molecular Structure
  • Monosaccharides / chemistry*
  • Oxidation-Reduction

Substances

  • Benzoates
  • Glycosides
  • Monosaccharides