An unusual caffeic acid derived bicyclic [2.2.2] octane lignan and other constituents from Cordia rufescens

Phytochemistry. 2012 Apr:76:158-61. doi: 10.1016/j.phytochem.2011.09.019. Epub 2012 Jan 14.

Abstract

This work reports isolation of an unusual lignan with a bicyclic [2.2.2] octene skeleton, named rufescenolide (1), from stems of Cordia rufescens, along with β-sitosterol, stigmasterol, syringaldehyde, 3-β-O-D-glucopyranosyl-sitosterol, methyl caffeate, 4-methoxy-protocatechuic acid and methyl rosmarinate. Structural characterizations employed IR spectroscopic, ESIHRMS and mono and dimensional NMR spectroscopy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bridged Bicyclo Compounds / chemistry
  • Bridged Bicyclo Compounds / isolation & purification*
  • Caffeic Acids / chemistry*
  • Cordia / chemistry*
  • Hydroxybenzoates / chemistry
  • Lignans / chemistry*
  • Lignans / isolation & purification
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Octanes / chemistry*
  • Octanes / isolation & purification
  • Plant Stems / chemistry
  • Sitosterols / chemistry
  • Sitosterols / isolation & purification
  • Stigmasterol / chemistry
  • Stigmasterol / isolation & purification

Substances

  • Bridged Bicyclo Compounds
  • Caffeic Acids
  • Hydroxybenzoates
  • Lignans
  • Octanes
  • Sitosterols
  • rufescenolide
  • protocatechuic acid
  • gamma-sitosterol
  • Stigmasterol