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 |
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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 |
format | Article |
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source | Free Full-Text Journals in Chemistry |
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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