Enantioselective synthesis of tetrafluorinated glucose and galactose

Org Lett. 2008 Sep 4;10(17):3673-6. doi: 10.1021/ol801272e. Epub 2008 Aug 1.

Abstract

Polyfluorinated carbohydrates have emerged as interesting probes to investigate "polar hydrophobicity" effect(s) in protein-carbohydrate interactions. A convenient enantioselective synthesis of tetrafluorinated analogues of two of the most important monosaccharides, D-glucose and D-galactose, is reported, as well as our first results regarding the glycosylation of these sugar analogues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Galactose / analogs & derivatives*
  • Galactose / chemical synthesis
  • Glucose / analogs & derivatives*
  • Glucose / chemical synthesis
  • Glycosylation
  • Hydrocarbons, Fluorinated / chemical synthesis
  • Stereoisomerism

Substances

  • Hydrocarbons, Fluorinated
  • Glucose
  • Galactose