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Issue 11, 2009
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Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water

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Abstract

Water was found to be a suitable reaction medium for the direct asymmetric aldol reaction of various cyclic ketones with aryl aldehydes catalyzed by a primary-tertiary diamine-Brønsted acid.

Graphical abstract: Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water

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Publication details

The article was received on 11 Aug 2009, accepted on 01 Sep 2009 and first published on 11 Sep 2009


Article type: Communication
DOI: 10.1039/B916583E
Citation: Green Chem., 2009,11, 1750-1753
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    Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water

    J. Lin, C. Zhang and J. Xiao, Green Chem., 2009, 11, 1750
    DOI: 10.1039/B916583E

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