Syntheses of alpha- and beta-C-glucopyranosyl serines from a common intermediate

Org Lett. 2008 Nov 6;10(21):4911-4. doi: 10.1021/ol802009v. Epub 2008 Sep 27.

Abstract

A versatile synthesis leading to either C-linked alpha- or beta-glucopyranosyl serines is presented from a common, advanced synthetic intermediate. Cyclization of the penultimate carbinol onto the alkene and methanolysis of the lactone yields selectively the alpha-linkage. A transposition of these last steps leads to the beta-linked isomer selectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Esterification
  • Glucose / chemistry*
  • Molecular Structure
  • Serine / analogs & derivatives*
  • Serine / chemical synthesis*
  • Serine / chemistry
  • Stereoisomerism

Substances

  • Serine
  • Glucose