Aromatic cations from oxidative carbon-hydrogen bond cleavage in bimolecular carbon-carbon bond forming reactions

J Org Chem. 2012 Aug 3;77(15):6574-82. doi: 10.1021/jo301185h. Epub 2012 Jul 16.

Abstract

Chromenes and isochromenes react quickly with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) to form persistent aromatic oxocarbenium ions through oxidative carbon-hydrogen cleavage. This process is tolerant of electron-donating and electron-withdrawing groups on the benzene ring and additional substitution on the pyran ring. A variety of nucleophiles can be added to these cations to generate a diverse set of structures.

Publication types

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

MeSH terms

  • Cations / chemical synthesis
  • Cations / chemistry
  • Hydrocarbons, Aromatic / chemical synthesis*
  • Hydrocarbons, Aromatic / chemistry
  • Molecular Structure
  • Oxidation-Reduction

Substances

  • Cations
  • Hydrocarbons, Aromatic