An Improved Helferich Method for the α/β-Stereoselective Synthesis of 4-Methylumbelliferyl Glycosides for the Detection of Microorganisms

Molecules. 2015 Dec 4;20(12):21681-99. doi: 10.3390/molecules201219789.

Abstract

An improved Helferich method is presented. It involves the glycosylation of 4-methyl-umbelliferone with glycosyl acetates in the presence of boron trifluoride etherate combined with triethylamine, pyridine, or 4-dimethylaminopyridine under mild conditions, followed by deprotection to give fluorogenic 4-methylumbelliferyl glycoside substrates. Due to the use of base, the glycosylation reaction proceeds more easily, is uncommonly α- or β-stereoselective, and affords the corresponding products in moderate to excellent yields (51%-94%) under appropriate conditions.

Keywords: 4-methylumbelliferyl glycosides; fluorogenic substrates; glycosyl acetates; peracetyl sugars; stereoselective glycosylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Aminopyridine / analogs & derivatives
  • 4-Aminopyridine / chemistry
  • Boranes / chemistry
  • Catalysis
  • Ethylamines / chemistry
  • Glycosides / chemical synthesis*
  • Glycosylation
  • Hymecromone / analogs & derivatives*
  • Hymecromone / chemical synthesis
  • Pyridines / chemistry
  • Stereoisomerism

Substances

  • 4-methylumbelliferyl glycosides
  • Boranes
  • Ethylamines
  • Glycosides
  • Pyridines
  • Hymecromone
  • boron trifluoride etherate
  • 4-Aminopyridine
  • pyridine
  • 4-dimethylaminopyridine
  • triethylamine