Recent Developments in the Catalytic Enantioselective Sakurai Reaction

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Authors: Hélène Pellissier
Cited by: 0
References: 63

Abstract

The Sakurai reaction constitutes a valuable tool for carbon–carbon bond formation. The use of nontoxic allylic reagents as well as the atom economy of the global process has prompted the development of enantioselective (aza)-variants based on the use of chiral organo- and metal catalysts. This review collects the recent developments in catalytic enantioselective Sakurai reactions published since the beginning of 2011, including methodologies based on the use of chiral organocatalysts, metal/boron catalysts and multicatalyst systems. It is divided into three parts, dealing successively with enantioselective organocatalytic (aza)-Sakurai reactions, enantioselective metal/boron-catalyzed Sakurai reactions and enantioselective multicatalyzed (aza)-Sakurai reactions. It shows that, although still widely developed with aromatic aldehydes, the enantioselective catalytic Sakurai reaction has considerably matured in the last decade.

Fields of Study & Subjects

Asymmetric Synthesis and Catalysis Axial and Atropisomeric Chirality Synthesis Catalytic Cross-Coupling Reactions

Publication details

Journal / source
Reactions
Volume
7
Issue
1
Pages
6–6
Publication date
10 January 2026
Language
EN