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Best design of heterogenized beta-aminoalcohols for improvement of enantioselective addition of diethylzinc to benzaldehyde
Journal article   Peer reviewed

Best design of heterogenized beta-aminoalcohols for improvement of enantioselective addition of diethylzinc to benzaldehyde

Sébastien Abramson, M. Lasperas, A. Galarneau, D. Desplantier-Giscard and D. Brunel
Chemical Communications, Vol.18
2000

Abstract

INORGANIC-ORGANIC CATALYSTS CHIRAL CATALYSTS ALDEHYDES DIALKYLZINCS ALKYLATION EPHEDRINE SILICAS ALUMINA
Covalent immobilization of (1R,2S)-(-)-ephedrine, used as a model molecule of beta-aminoalcohols, on the surface of MCM-41-type mesoporous aluminosilicates, performed by a new sol-gel method, leads to chiral auxiliaries which show greatly enhanced rates and ee's compared to those reported up to now in the enantioselective addition of diethylzinc to benzaldehyde.
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