Issue 8, 1989

Asymmetric synthesis of optically active β-substituted ketones by highly enantioselective catalytic conjugate addition of dialkylzinc reagents to enones using a catalyst system of nickel(II)-chiral ligand–achiral ligand in acetonitrile/toluene

Abstract

Highly enantioselective conjugate addition of dialkylzinc reagents to aryl substituted enones using Ni(II)-bipyridyl–chiral ligand in acetonitrile (MeCN)/toluene as an in situ prepared catalyst system affords β-substituted ketones in up to 90% enantiomeric excess (e.e.).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 516-517

Asymmetric synthesis of optically active β-substituted ketones by highly enantioselective catalytic conjugate addition of dialkylzinc reagents to enones using a catalyst system of nickel(II)-chiral ligand–achiral ligand in acetonitrile/toluene

K. Soai, T. Hayasaka and S. Ugajin, J. Chem. Soc., Chem. Commun., 1989, 516 DOI: 10.1039/C39890000516

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