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Current Organic Chemistry

Editor-in-Chief

ISSN (Print): 1385-2728
ISSN (Online): 1875-5348

Recent Development in the Asymmetric Michael Addition for Carbon-Carbon Bond Formation

Author(s): Majid M. Heravi, Parvin Hajiabbasi and Hoda Hamidi

Volume 18, Issue 4, 2014

Page: [489 - 511] Pages: 23

DOI: 10.2174/13852728113176660149

Price: $65

Abstract

Attempts to induce stereoselectivity in the conjugate addition to the α,β-unsaturated acceptors have been investigated by numerous research groups, classically through the use of either a chiral acceptor or chiral donor component in the reaction. The asymmetric Michael addition catalyzed by chiral catalysts has been extensively proven and established to be a powerful synthetic tool for especially a range of asymmetric syntheses of natural products and various heterocyclic systems.

This review covers the recent reports and further applications of this methodology in the formation of carbon-carbon bond between or within functionalized and sensitive substrates which provides new opportunities, mainly in the total synthesis, medicinal and process chemistry, nanotechnology and chemical biology.

Keywords: Asymmetric conjugation, C-C bond formation, chiral reagent, chiral catalyst, enolizable carbonyl derivatives, Michael addition.


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