Pd-catalyzed α-selective C(sp3)-H acetoxylation of amides through an unusual cyclopalladation mechanism

Chem Commun (Camb). 2015 Feb 21;51(15):3219-22. doi: 10.1039/c4cc09576f.

Abstract

We report the first example of Pd-catalyzed site-selective α-C(sp(3))-H oxidation/acetoxylation of amides through an unusual [4,6]-bicyclic metallacycle intermediate with 1-aminoanthraquinone as a new bidentate directing group. In addition to the distinct mechanism and high efficiency, the reaction is highly appealing due to the ample commercial source, low-cost, as well as easy removal and recycling of the auxiliary group.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry*
  • Anthraquinones / chemistry*
  • Catalysis
  • Hydrogen / chemistry
  • Oxidation-Reduction
  • Palladium / chemistry*

Substances

  • Amides
  • Anthraquinones
  • Palladium
  • Hydrogen
  • 1-aminoanthraquinone