Facile synthesis of (Z) tetracos-5-enoic acid and racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid

GD Coxon, JD Douglas, David Minnikin

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

(Z)-tetracos-5-enoic acid and racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid have been prepared from 1-eicosene by a new facile route. Periodic acid cleavage of the epoxide of 1-eicosene gave nonadecanal which was condensed with 4-carboxybutyltriphenylphosphonium bromide to give predominately (Z)-tetracos-5-enoic acid. Simmons-Smith type cyclopropanation of (Z)-tetracos-5-enoic acid gave a minor proportion of racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid accompanied by major amounts of its methyl ester.
Original languageEnglish
Pages (from-to)49-53
Number of pages5
JournalChemistry and Physics of Lipids
Volume126
Issue number1
DOIs
Publication statusPublished - 1 Nov 2003

Keywords

  • alkene stereochemistry
  • fatty acids
  • mycolic acids
  • cyclopropane rings
  • Wittig reaction

Fingerprint

Dive into the research topics of 'Facile synthesis of (Z) tetracos-5-enoic acid and racemic cis-4-(2-octadecylcyclopropane-1-yl)-butanoic acid'. Together they form a unique fingerprint.

Cite this