FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes

Chem Commun (Camb). 2013 Sep 21;49(73):8051-3. doi: 10.1039/c3cc43159b. Epub 2013 Aug 1.

Abstract

Highly substituted indene derivatives were readily prepared in excellent yields with high regioselectivity under very mild reaction conditions by the FeCl3 mediated intramolecular olefin-cationic cyclization of cinnamates.

MeSH terms

  • Alkenes / chemistry*
  • Cations
  • Cinnamates / chemistry*
  • Cyclization
  • Indenes / chemical synthesis
  • Indenes / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Alkenes
  • Cations
  • Cinnamates
  • Indenes