Highly efficient synthesis of flavonol 5-O-glycosides with glycosyl ortho-alkynylbenzoates as donors

Org Biomol Chem. 2016 Jan 28;14(4):1221-5. doi: 10.1039/c5ob02313k. Epub 2015 Dec 16.

Abstract

With glycosyl ortho-alkynylbenzoates as donors, the highly efficient glycosylation of flavonoid 5-OH which are notorious for their low reactivity due to their involvement in the formation of strong intramolecular H-bonds was achieved under the catalysis of a Au(i) complex. Thus, a series of flavonoid 5-O-glycosides, including a kaempferol 5-O-disaccharide, were synthesized with good to excellent yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Benzoates / chemistry*
  • Flavonols / chemical synthesis*
  • Flavonols / chemistry
  • Glycosides / chemical synthesis*
  • Glycosides / chemistry
  • Glycosylation
  • Molecular Structure

Substances

  • Alkynes
  • Benzoates
  • Flavonols
  • Glycosides