Logo image
Home Academic units
Sign in
Highly practical and enantioselective cu-catalyzed conjugate addition of alkylzinc reagents to cyclic enones at ambient temperature
Journal article   Peer reviewed

Highly practical and enantioselective cu-catalyzed conjugate addition of alkylzinc reagents to cyclic enones at ambient temperature

Isaac J Krauss and James L Leighton
Organic letters, Vol.5(18), pp.3201-3203
09/01/2003
PMID: 12943387

Abstract

Ligands Stereoselectivity Substitution reactions Conjugate acid-base pairs Enones
A new ligand for Cu-catalyzed enantioselective additions of dialkylzincs to cyclic enones has been developed. In addition to providing good to excellent enantioselectivities with a range of cyclic enones and dialkylzincs, the ligand has several notworthy features: it can be readily prepared in just two steps, is an air-stable crystalline solid, and provides optimal performance at ambient temperature.

Metrics

35 Record Views

Details