Stereochemistry and rearrangement reactions of hydroxylignanolactones

Org Biomol Chem. 2008 Jul 21;6(14):2619-27. doi: 10.1039/b801593g. Epub 2008 May 19.

Abstract

Various conflicting data on the rearrangement and absolute stereochemistry of hydroxylignano-9,7'-lactones are resolved using 18O labeled compounds, also confirmed by an X-ray analysis of a pure lignano-9,7'-lactone enantiomer, obtained for the first time. Under NaH/DMF rearrangement conditions a silyl protected hydroxylignano-9,9'-lactone underwent an unexpected silyl migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ethanol / chemistry
  • Furans / chemistry
  • Lactones / chemistry*
  • Lignans / chemistry
  • Mass Spectrometry
  • Oxygen Isotopes
  • Protons
  • Sodium Hydroxide / chemistry
  • Stereoisomerism
  • Water / chemistry

Substances

  • Furans
  • Lactones
  • Lignans
  • Oxygen Isotopes
  • Protons
  • Water
  • Ethanol
  • Sodium Hydroxide
  • matairesinol