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Issue 8, 2008
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Catalytic asymmetric aldol reactions in aqueous media

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Abstract

Nature has perfected the stereospecific aldol reaction by using aldolase enzymes. While virtually all the biochemical aldol reactions use unmodified donor and acceptor carbonyls and take place under catalytic control in an aqueous environment, the chemical domain of the aldol addition has mostly relied on prior transformation of carbonyl substrates, and the whole process traditionally is carried out in anhydrous solvents. The area of aqua-asymmetric aldol reactions has received much attention recently in light of the perception both of its green chemistry advantages and its analogy to eon-perfected enzyme catalysis. Both chiral metal complexes and small chiral organic molecules have been recently reported to catalyze aldol reactions with relatively high chemical and stereochemical efficiency. This tutorial review describes recent developments in this area.

Graphical abstract: Catalytic asymmetric aldol reactions in aqueous media

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Publication details

The article was received on 21 Apr 2008 and first published on 09 Jun 2008


Article type: Tutorial Review
DOI: 10.1039/B710577K
Citation: Chem. Soc. Rev., 2008,37, 1502-1511
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    Catalytic asymmetric aldol reactions in aqueous media

    J. Mlynarski and J. Paradowska, Chem. Soc. Rev., 2008, 37, 1502
    DOI: 10.1039/B710577K

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