DDQ-promoted direct transformation of benzyl hydrocarbons to amides via tandem reaction of the CDC reaction and Beckmann rearrangement

Org Biomol Chem. 2013 Sep 28;11(36):6008-12. doi: 10.1039/c3ob41218k.

Abstract

An atom-efficient and transition metal-free approach to amides from the corresponding benzyl hydrocarbons through C-H and C-C bond cleavage has been developed. Mechanistic studies have shown that a DDQ-promoted cross-dehydrogenative coupling (CDC) reaction with subsequent oxidation and rearrangement are involved in this transformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemical synthesis*
  • Amides / chemistry
  • Benzoquinones / chemistry*
  • Hydrocarbons, Aromatic / chemistry*
  • Hydrogenation
  • Molecular Structure
  • Oxidation-Reduction

Substances

  • Amides
  • Benzoquinones
  • Hydrocarbons, Aromatic
  • dichlorodicyanobenzoquinone