Enantioselective Copper-Catalyzed Allylic/Propargylic Acyloxylation: Asymmetric Variants of the Kharasch–Sosnovsky Reaction

Abstract Copper-catalyzed enantioselective allylic/propargylic acyloxylation, evolving from the classical Kharasch–Sosnovsky reaction, has emerged as a versatile strategy for the stereocontrolled synthesis of chiral esters. This short review comprehensively summarizes recent advances in asymmetric variants of Kharasch–Sosnovsky reaction across three primary substrate categories: cyclic olefins, acyclic alkenes/alkynes, and 1,3-dienes/enynes, with particular emphasis on substrate scope and mechanistic insights.

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Publication Details

Journal
Synthesis
Published
2025-06-06
DOI
https://doi.org/10.1055/a-2630-0589
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Enantioselective Copper-Catalyzed Allylic/Propargylic Acyloxylation: Asymmetric Variants of the Kharasch–Sosnovsky Reaction

Shouyun Yu, Sheng Tang
Synthesis
Catalytic Alkyne Reactions
article

Enantioselective Copper-Catalyzed Allylic/Propargylic Acyloxylation: Asymmetric Variants of the Kharasch–Sosnovsky Reaction

Shouyun Yu, Sheng Tang
article en

Abstract

Abstract Copper-catalyzed enantioselective allylic/propargylic acyloxylation, evolving from the classical Kharasch–Sosnovsky reaction, has emerged as a versatile strategy for the stereocontrolled synthesis of chiral esters. This short review comprehensively summarizes recent advances in asymmetric variants of Kharasch–Sosnovsky reaction across three primary substrate categories: cyclic olefins, acyclic alkenes/alkynes, and 1,3-dienes/enynes, with particular emphasis on substrate scope and mechanistic insights.

SynthesisVol. 57(18)
State Key Laboratory of Analytical Chemistry for Life Science (CN), Nanjing University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 90%
Catalytic Alkyne Reactions
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