Nickel-Catalyzed Esterification of Aliphatic Amides

Angew Chem Int Ed Engl. 2016 Nov 21;55(48):15129-15132. doi: 10.1002/anie.201607856. Epub 2016 Nov 4.

Abstract

Recent studies have demonstrated that amides can be used in nickel-catalyzed reactions that lead to cleavage of the amide C-N bond, with formation of a C-C or C-heteroatom bond. However, the general scope of these methodologies has been restricted to amides where the carbonyl is directly attached to an arene or heteroarene. We now report the nickel-catalyzed esterification of amides derived from aliphatic carboxylic acids. The transformation requires only a slight excess of the alcohol nucleophile and is tolerant of heterocycles, substrates with epimerizable stereocenters, and sterically congested coupling partners. Moreover, a series of amide competition experiments establish selectivity principles that will aid future synthetic design. These studies overcome a critical limitation of current Ni-catalyzed amide couplings and are expected to further stimulate the use of amides as synthetic building blocks in C-N bond cleavage processes.

Keywords: aliphatic amides; cross-coupling; esterification; homogeneous catalysis; nickel.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amides / chemistry*
  • Catalysis
  • Esters / chemical synthesis*
  • Esters / chemistry
  • Molecular Conformation
  • Nickel / chemistry*
  • Organometallic Compounds / chemistry*

Substances

  • Amides
  • Esters
  • Organometallic Compounds
  • Nickel