Synthesis 2012; 44(10): 1453-1463
DOI: 10.1055/s-0031-1290981
short review
© Georg Thieme Verlag Stuttgart · New York

Organocatalytic Asymmetric Vinylogous Aldol Reactions

Vishnumaya Bisai*
Department of Applied Sciences, National Institute of Technical Teachers’ Training and Research (NITTTR) Bhopal, Shamla Hills, Bhopal, MP-462 002, India, Fax: +91(755)4092392   Email: vishnumayabisai@gmail.com
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Further Information

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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