Asymmetric Michael addition catalyzed by a cinchona alkaloid derivative non-covalently immobilized on layered inorganic supports

A study on the asymmetric Michael addition of a fluorine containing carbon nucleophile to β-nitrostyrene was carried out to find an easily obtainable cinchona alkaloid derivative, which provides high stereoselectivities, and may be conveniently immobilized over inorganic materials to obtain efficien...

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Bibliographic Details

Published in:	Reaction kinetics, mechanisms and catalysis Vol. 121; no. 1; pp. 293 - 306
Main Authors:	Szőllősi, György, Kovács, Lenke, Kozma, Viktória, Kolcsár, Vanessza Judit
Format:	Journal Article
Language:	English
Published:	Dordrecht Springer Netherlands 01-06-2017
Subjects:	Catalysis Chemistry Chemistry and Materials Science Industrial Chemistry/Chemical Engineering Physical Chemistry Michael addition Asymmetric Heterogeneous Inorganic–organic hybrid Cinchona alkaloid Organocatalyst
Online Access:	Get full text
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