Asymmetric organocatalytic direct aldol reactions of cyclohexanone with aldehydes in brine

Organocatalytic asymmetric direct aldol reactions in brine with high diastereo- and enantioselectivities, using a readily available bifunctional amide catalyst, were developed.Key words: aldol reaction, organocatalyst, asymmetric catalysis, water.

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Veröffentlicht in:Canadian journal of chemistry 2007-03, Vol.85 (3), p.208-213
Hauptverfasser: Huang, Wen-Ping, Chen, Jia-Rong, Li, Xin-Yong, Cao, Yi-Ju, Xiao, Wen-Jing
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container_title Canadian journal of chemistry
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creator Huang, Wen-Ping
Chen, Jia-Rong
Li, Xin-Yong
Cao, Yi-Ju
Xiao, Wen-Jing
description Organocatalytic asymmetric direct aldol reactions in brine with high diastereo- and enantioselectivities, using a readily available bifunctional amide catalyst, were developed.Key words: aldol reaction, organocatalyst, asymmetric catalysis, water.
doi_str_mv 10.1139/v07-012
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subjects Aldehydes
Brines
Catalysis
Catalysts
Chemical properties
Chemical reactions
Cyclohexanol
Fructosediphosphate aldolase
Studies
Water
title Asymmetric organocatalytic direct aldol reactions of cyclohexanone with aldehydes in brine
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