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DOI: 10.1055/s-0031-1290981
Organocatalytic Asymmetric Vinylogous Aldol Reactions
Publication History
Received: 23 February 2012
Accepted after revision: 05 April 2012
Publication Date:
24 April 2012 (online)
Dedicated respectfully to Professor Vinod K. Singh, Indian Institute of Science Education and Research (IISER) Bhopal, India
Abstract
The aldol reaction is one of the most predominantly used reactions for the formation of C–C bonds in synthetic organic chemistry. The vinylogous extension of this fundamental C–C bond-forming reaction to nucleophilic components, such as the vinylogous aldol reaction is significant because it provides rapid access to polyketide derivatives such as δ-hydroxy-β-keto esters and α,β-unsaturated δ-hydroxy carbonyl compounds. Further transformation of these compounds can be accomplished with good diastereoselectivity and leads the way to polyol units, a motif common to many pharmaceutically important natural products. Details of recent advances in the organocatalytic vinylogous aldol reaction and its applications are discussed in this review.
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For organocatalytic direct aldol reactions, see:
For recent reviews on organocatalytic direct aldol reactions, see:
For reviews, see:
For vinylogous retro aldol reactions, see:
For recent reviews of vinylogous aldol reactions, see:
For enantioselective catalysis of vinylogous aldol reaction of 2-(silyloxy)furans, see:
For example, see: