Visible-light-mediated decarboxylation/oxidative amidation of α-keto acids with amines under mild reaction conditions using O(2)

Angew Chem Int Ed Engl. 2014 Jan 7;53(2):502-6. doi: 10.1002/anie.201308614. Epub 2013 Nov 24.

Abstract

Photochemistry has ushered in a new era in the development of chemistry, and photoredox catalysis has become a hot topic, especially over the last five years, with the combination of visible-light photoredox catalysis and radical reactions. A novel, simple, and efficient radical oxidative decarboxylative coupling with the assistant of the photocatalyst [Ru(phen)3 ]Cl2 is described. Various functional groups are well-tolerated in this reaction and thus provides a new approach to developing advanced methods for aerobic oxidative decarboxylation. The preliminary mechanistic studies revealed that: 1) an SET process between [Ru(phen)3 ](2+) * and aniline play an important role; 2) O2 activation might be the rate-determining step; and 3) the decarboxylation step is an irreversible and fast process.

Keywords: amides; computational chemistry; photochemistry; reaction mechanism; synthetic methods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry*
  • Amines / chemistry*
  • Aniline Compounds / chemistry
  • Catalysis
  • Decarboxylation / radiation effects
  • Hydrocarbons, Chlorinated / chemistry
  • Keto Acids / chemistry*
  • Light*
  • Molecular Structure
  • Oxidation-Reduction
  • Oxygen / chemistry*
  • Photochemistry
  • Ruthenium

Substances

  • Amides
  • Amines
  • Aniline Compounds
  • Hydrocarbons, Chlorinated
  • Keto Acids
  • Ruthenium
  • Oxygen
  • aniline