Convenient method for the addition of disulfides to alkenes

Bioorg Med Chem Lett. 2007 Nov 15;17(22):6197-201. doi: 10.1016/j.bmcl.2007.09.021. Epub 2007 Sep 8.

Abstract

Catalytic disulfenylation reaction of alkenes by common Lewis acids has been investigated in detail. While reactions by FeCl(3) were feasible with cycloalkenes and other simple alkenes, much faster and excellent conversions were possible by AlCl(3) even with the substrates less reactive toward FeCl(3).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Chlorides
  • Cycloparaffins / chemistry
  • Disulfides / chemistry*
  • Ferric Compounds / chemistry
  • Molecular Structure

Substances

  • Alkenes
  • Chlorides
  • Cycloparaffins
  • Disulfides
  • Ferric Compounds
  • ferric chloride