Asymmetric synthesis of highly substituted β-lactones through oxidative carbene catalysis with LiCl as cooperative Lewis acid

Angew Chem Int Ed Engl. 2014 Sep 1;53(36):9622-6. doi: 10.1002/anie.201405200. Epub 2014 Jul 11.

Abstract

The reaction of enals with β-diketones, β-ketoesters, and malonates bearing a β-oxyalkyl substituent at the α-position by oxidative NHC catalysis to provide highly substituted β-lactones is described. Reactions occur with excellent diastereo- and enantioselectivity. The organo cascade comprises two CC bond formations and one CO bond formation. Up to four contiguous stereogenic centers including two fully substituted stereocenters are formed in the cascade.

Keywords: N-heterocyclic carbenes; asymmetric synthesis; cooperative catalysis; organo catalysis; β-lactones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cyclohexanes / chemistry
  • Lactones / chemical synthesis*
  • Lewis Acids / chemistry*
  • Lithium Chloride / chemistry*
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Oxidants / chemistry
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • Cyclohexanes
  • Lactones
  • Lewis Acids
  • Oxidants
  • carbene
  • Lithium Chloride
  • Methane