Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

Org Biomol Chem. 2010 Aug 21;8(16):3624-6. doi: 10.1039/c004672h. Epub 2010 Jun 30.

Abstract

The bis-THF cores of annonaceous acetogenins were synthesized using (3R,4R)-1,5-hexadiene-3,4-diol (1) as the sole source of carbon atoms. The methylene acetal function was applied as a new linker/tether to facilitate the ring-closing metathesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetogenins / chemistry*
  • Cross-Linking Reagents / chemistry
  • Furans / chemical synthesis*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Acetogenins
  • Cross-Linking Reagents
  • Furans
  • tetrahydrofuran