Oxidation of oximes to nitrile oxides with hypervalent iodine reagents

Org Lett. 2009 Apr 2;11(7):1539-42. doi: 10.1021/ol900194v.

Abstract

Iodobenzene diacetate in MeOH containing a catalytic amount of TFA efficiently oxidizes aldoximes to nitrile oxides. The latter may be trapped in situ with olefins in a bimolecular or an intramolecular mode. The new method enables the execution of tandem oxidative dearomatization of phenols/intramolecular nitrile oxide cycloaddition sequences leading to useful synthetic intermediates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Combinatorial Chemistry Techniques
  • Cyclization
  • Hydrocarbons, Iodinated / chemistry*
  • Molecular Structure
  • Nitriles / chemistry*
  • Oxidation-Reduction
  • Oxides / chemistry
  • Oximes / chemistry*

Substances

  • Hydrocarbons, Iodinated
  • Nitriles
  • Oxides
  • Oximes