Asymmetric Alkoxycarbonyl-Cyanation of Styrenes via Photoredox and Copper Catalysis

A photoredox and copper dual-catalyzed alkoxycarbonyl-cyanation of styrenes is developed. With this method, a wide range of chiral β-aryl-substituted β-cyanoester derivatives is obtained in good yields with high enantioselectivities. Optically pure β-cyanoesters can be readily converted to the corresponding chiral β-substituted γ-amino acid derivatives. With this strategy in mind, two marketed drugs, (R)-baclofen and (R)-phenibut, are synthesized through the efficient transformation of their corresponding chiral β-aryl-substituted β-cyanoesters. We expect that this efficient and convenient method for synthesizing structurally diverse chiral β-cyanoester derivatives can accelerate the drug development process.

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Publication Details

Journal
ACS Catalysis
Published
2025-07-18
DOI
https://doi.org/10.1021/acscatal.5c04002
Citations
6
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
5.62
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article

Asymmetric Alkoxycarbonyl-Cyanation of Styrenes via Photoredox and Copper Catalysis

Ping Liang, Jie Wu, Zhipeng Zong, Jian‐Qiang Chen et al.
6 citations
ACS Catalysis
Catalytic C–H Functionalization Methods
5.62
article

Asymmetric Alkoxycarbonyl-Cyanation of Styrenes via Photoredox and Copper Catalysis

Ping Liang, Jie Wu, Zhipeng Zong, Jian‐Qiang Chen, J. Yao
article en
6 citations

Abstract

A photoredox and copper dual-catalyzed alkoxycarbonyl-cyanation of styrenes is developed. With this method, a wide range of chiral β-aryl-substituted β-cyanoester derivatives is obtained in good yields with high enantioselectivities. Optically pure β-cyanoesters can be readily converted to the corresponding chiral β-substituted γ-amino acid derivatives. With this strategy in mind, two marketed drugs, (R)-baclofen and (R)-phenibut, are synthesized through the efficient transformation of their corresponding chiral β-aryl-substituted β-cyanoesters. We expect that this efficient and convenient method for synthesizing structurally diverse chiral β-cyanoester derivatives can accelerate the drug development process.

ACS CatalysisVol. 15(15)
Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), Taizhou University (CN)
Openalex Percentile: Top 4%
Catalytic C–H Functionalization Methods
5.62
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