Asymmetric Chlorination of β-Keto Esters Using Diaminomethylenemalononitrile Organocatalyst

Chem Pharm Bull (Tokyo). 2016;64(12):1781-1784. doi: 10.1248/cpb.c16-00722.

Abstract

Diaminomethylenemalononitrile organocatalysts promote the asymmetric chlorination of simple cyclic β-keto esters such as methyl, ethyl, and benzyl esters of 1-oxo-2,3-dihydro-1H-indene-2-carboxylic acid. This affords the corresponding chiral α-chlorinated carbonyl products in excellent yields with high enantioselectivities.

MeSH terms

  • Catalysis
  • Diamines / chemistry*
  • Esters / chemistry*
  • Halogenation*
  • Hydrocarbons, Chlorinated / chemical synthesis*
  • Hydrocarbons, Chlorinated / chemistry
  • Molecular Structure
  • Nitriles / chemistry*
  • Stereoisomerism

Substances

  • Diamines
  • Esters
  • Hydrocarbons, Chlorinated
  • Nitriles