Nickel-catalyzed amination of aryl pivalates by the cleavage of aryl C-O bonds

Angew Chem Int Ed Engl. 2010 Apr 6;49(16):2929-32. doi: 10.1002/anie.200907287. Epub 2010 Mar 12.

Abstract

Catalytic amination: The title reaction demonstrates the use of aryl carboxylates as suitable electrophilic coupling substrates in catalytic amination reactions. N-heterocyclic carbene ligands and NaOtBu promote the amination of aryl pivalates through the cleavage of normally unreactive aryl carbon-oxygen bonds (see scheme; cod=cyclooctadiene).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Catalysis
  • Heterocyclic Compounds / chemistry*
  • Molecular Structure
  • Nickel / chemistry*
  • Pentanoic Acids / chemistry*

Substances

  • Heterocyclic Compounds
  • Pentanoic Acids
  • Nickel
  • pivalic acid