Asymmetric Organocatalytic Tandem/Domino Reactions to Access Bioactive Products

(E-pub Ahead of Print)

Author(s): Hélène Pellissier*

Journal Name: Current Organic Chemistry


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Abstract:

Tandem and domino reactions constitute economic routes to complex molecules starting from simple materials. Especially, combining these powerful procedures to asymmetric catalysis allow a direct access to many elaborated chiral products, including important key intermediates in total syntheses of important biologically active compounds. A range of various types of chiral organocatalysts have already been successfully applied to such syntheses. This review presents major developments in the total synthesis of bioactive products based on the use of enantioselective organocatalytic domino/tandem reactions as key steps. It is divided into three parts, dealing successively with syntheses based on organocatalytic asymmetric Michael-initiated domino reactions as key steps; aldol-initiated domino/tandem reactions and other domino reactions.

Keywords: total synthesis, bioactive products, enantioselective domino/tandem reactions, organocatalysis, asymmetric catalysis, chirality.

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Article Details

(E-pub Ahead of Print)
DOI: 10.2174/1385272825666210208142427
Price: $95

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