Novel cycloaddition reaction of [60]fullerene with carbonyl ylides generated from epoxides

J Org Chem. 2006 May 26;71(11):4346-8. doi: 10.1021/jo060427+.

Abstract

The thermal reaction of [60]fullerene (C60) with the carbonyl ylides generated in situ from trans-epoxides to give C60-fused tetrahydrofuran derivatives has been investigated. The reaction of C60 with trans-2-benzoyl-3-aryloxiranes afforded only cis-products, while the reaction of C60 with 2-cyano-2-ethoxycarbonyl-3-aryloxiranes gave exclusively or predominantly cis isomers. The isomeric distributions of the latter reactions were drastically affected by the substituent on the phenyl ring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Epoxy Compounds / chemistry*
  • Fullerenes / chemistry*
  • Furans / chemistry
  • Molecular Structure

Substances

  • Epoxy Compounds
  • Fullerenes
  • Furans
  • fullerene C60