Nickel-catalyzed selective conversion of two different aldehydes to cross-coupled esters

J Am Chem Soc. 2011 Apr 6;133(13):4668-71. doi: 10.1021/ja109908x. Epub 2011 Mar 15.

Abstract

In the presence of a Ni(0)/NHC catalyst, an equimolar mixture of aliphatic and aryl aldehydes can be employed to selectively yield a single cross-coupled ester. This reaction can be applied to a variety of aliphatic (1°, 2°, cyc-2°, and 3°) and aryl aldehyde combinations. The reaction represents 100% atom efficiency and generates no waste. Mechanistic studies have revealed that the striking feature of the reaction is the simultaneous coordination of two aldehydes to Ni(0).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry*
  • Catalysis
  • Esters / chemical synthesis*
  • Esters / chemistry
  • Molecular Structure
  • Nickel / chemistry*
  • Stereoisomerism

Substances

  • Aldehydes
  • Esters
  • Nickel