Reactive intermediates from DMDO oxidation of ynamides. Trapping of a de novo chiral push-pull carbene via cyclopropanation

Org Lett. 2008 Feb 21;10(4):661-3. doi: 10.1021/ol703083k. Epub 2008 Jan 17.

Abstract

The reaction profile of DMDO oxidations of ynamides is described. This work illustrates the first examples of highly diastereoselective intramolecular cyclopropanations of a push-pull carbene derived from alkyne oxidation. In addition, the ynamide oxidation provides facile access to ketoimides and reveals mechanistic insights into the chemistry of electronically biased oxirenes.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cyclopropanes / chemistry*
  • Epoxy Compounds / chemistry*
  • Hydrocarbons / chemistry
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Molecular Structure
  • Oxazoles / chemistry*
  • Oxidation-Reduction

Substances

  • Cyclopropanes
  • Epoxy Compounds
  • Hydrocarbons
  • Oxazoles
  • carbene
  • Methane
  • dimethyldioxirane