Cobalt-Catalyzed Enantioselective Dicarbofunctionalization of Acrylates

Catalytic enantioselective alkene difunctionalization represents a powerful tool for the rapid assembly of complex chiral molecules and has found wide range of applications in synthetic chemistry. Enantioselective control of the newly formed pro-chiral carbon centers using chiral cobalt catalyst, however, remains challenging. Herein, we report the first cobalt-catalyzed enantioselective difunctionalization of industry-relevant acrylates with lithium aryl boronates and α,α-dialkyl bromoacetate for the preparation of enantioenriched glutaric acid derivatives. Facile transformations of the resulting α-aryl esters to other functionalities have been achieved. To further showcase the synthetic utility of the current protocol, application to the enantioselective synthesis of an analog of (−)-preclamol was demonstrated.

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Publication Details

Journal
ACS Catalysis
Published
2024-10-02
DOI
https://doi.org/10.1021/acscatal.4c03670
Citations
5
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.25

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article

Cobalt-Catalyzed Enantioselective Dicarbofunctionalization of Acrylates

Yi Xu, Jiejun Li, Xiaolong Wan, Qilong Shen
5 citations
ACS Catalysis
Catalytic C–H Functionalization Methods
1.25
article

Cobalt-Catalyzed Enantioselective Dicarbofunctionalization of Acrylates

Yi Xu, Jiejun Li, Xiaolong Wan, Qilong Shen
article en
5 citations

Abstract

Catalytic enantioselective alkene difunctionalization represents a powerful tool for the rapid assembly of complex chiral molecules and has found wide range of applications in synthetic chemistry. Enantioselective control of the newly formed pro-chiral carbon centers using chiral cobalt catalyst, however, remains challenging. Herein, we report the first cobalt-catalyzed enantioselective difunctionalization of industry-relevant acrylates with lithium aryl boronates and α,α-dialkyl bromoacetate for the preparation of enantioenriched glutaric acid derivatives. Facile transformations of the resulting α-aryl esters to other functionalities have been achieved. To further showcase the synthetic utility of the current protocol, application to the enantioselective synthesis of an analog of (−)-preclamol was demonstrated.

ACS CatalysisVol. 14(20)
Shanghai Institute of Organic Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, National Key Research and Development Program of China
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
1.25
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