Absolute configurations of isoflavan-4-ol stereoisomers

Bioorg Med Chem Lett. 2008 Mar 15;18(6):1952-7. doi: 10.1016/j.bmcl.2008.01.116. Epub 2008 Feb 2.

Abstract

Isoflavan-4-ol has been synthesized quantitatively from the reduction of isoflavone in the presence of Pd/C and ammonium formate under N(2) atmosphere. Isolation of cis- and trans-isomers was achieved by flash column chromatography and each enantiomer was separated by Sumi-Chiral column chromatography. Absolute configurations of four stereoisomers were determined by circular dichroism spectroscopy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Circular Dichroism
  • Isoflavones / chemistry*
  • Isoflavones / metabolism
  • Molecular Structure
  • Spectrophotometry, Ultraviolet
  • Stereoisomerism

Substances

  • Isoflavones