Dinickel-Catalyzed Regio- and Enantioselective α-Alkylation of Acyclic Dialkylketone with Unactivated Alkyl Iodides

Abstract Asymmetric α-alkylation of ketones is a powerful synthetic tool; however, its application to challenging substrates, such as acyclic dialkyl ketones and unactivated alkyl electrophiles is limited. We describe a catalytic system employing a dinickel(I) complex that facilitates the enantioselective α-alkylation of acyclic dialkyl ketones using unactivated alkyl iodides. This method efficiently constructs ketones with quaternary carbon stereocenters in high yield while demonstrating outstanding levels of chemo-, regio-, and enantiocontrol.

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Publication Details

Journal
Synthesis
Published
2026-03-11
DOI
https://doi.org/10.1055/a-2826-1291
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Dinickel-Catalyzed Regio- and Enantioselective α-Alkylation of Acyclic Dialkylketone with Unactivated Alkyl Iodides

Liangwei Zhu, Zhonglin Tao, Dingyuhan Chen
Synthesis
Catalytic C–H Functionalization Methods
article

Dinickel-Catalyzed Regio- and Enantioselective α-Alkylation of Acyclic Dialkylketone with Unactivated Alkyl Iodides

Liangwei Zhu, Zhonglin Tao, Dingyuhan Chen
article en

Abstract

Abstract Asymmetric α-alkylation of ketones is a powerful synthetic tool; however, its application to challenging substrates, such as acyclic dialkyl ketones and unactivated alkyl electrophiles is limited. We describe a catalytic system employing a dinickel(I) complex that facilitates the enantioselective α-alkylation of acyclic dialkyl ketones using unactivated alkyl iodides. This method efficiently constructs ketones with quaternary carbon stereocenters in high yield while demonstrating outstanding levels of chemo-, regio-, and enantiocontrol.

Synthesis
Hunan University (CN)
Openalex Percentile: Top 24%
Catalytic C–H Functionalization Methods
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