Enantioselective copper-catalysed defluorinative alkylation of polyfluoroarenes with alkenes and 1,3-dienes

Despite impressive advances in the field of defluorinative alkylation of polyfluoroarenes, the corresponding asymmetric counterpart has remained a formidable challenge. Herein, we present the first example of asymmetric defluorinative alkylation of polyfluoroarenes with readily accessible alkenes, 1,3-dienes, and even (<i>Z</i>/<i>E</i>)-mixed 1,3-dienes as potential nucleophiles in the presence of a chiral CuH catalyst, avoiding the conventional utilization of highly reactive organometallics. This method enables the efficient construction of the challenging chiral Csp<sup>3</sup>-C<sub>ArF</sub> bond with outstanding stereocontrol (up to 99% ee in most cases). This reaction proceeds under mild reaction conditions, demonstrating excellent functional group compatibility and high regio- and stereoselectivity. Experimental studies in conjunction with density functional theory (DFT) calculations were carried out to unravel the plausible mechanism and elucidate the origins of excellent enantioselectivity.

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Journal
Chemical Science
Published
2025-11-25
DOI
https://doi.org/10.1039/d5sc08090h
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
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article

Enantioselective copper-catalysed defluorinative alkylation of polyfluoroarenes with alkenes and 1,3-dienes

Jiaqiong Sun, Ying Jiang, Xiuping Yuan, Lihan Zhu et al.
Chemical Science
Catalytic C–H Functionalization Methods
article

Enantioselective copper-catalysed defluorinative alkylation of polyfluoroarenes with alkenes and 1,3-dienes

Jiaqiong Sun, Ying Jiang, Xiuping Yuan, Lihan Zhu, Qian Zhang, Xiaoyu Li, Shucheng Ma, Tao Xiong, Dazhen Shi, Jianjun Yin, Simin Wang
article en

Abstract

Despite impressive advances in the field of defluorinative alkylation of polyfluoroarenes, the corresponding asymmetric counterpart has remained a formidable challenge. Herein, we present the first example of asymmetric defluorinative alkylation of polyfluoroarenes with readily accessible alkenes, 1,3-dienes, and even (<i>Z</i>/<i>E</i>)-mixed 1,3-dienes as potential nucleophiles in the presence of a chiral CuH catalyst, avoiding the conventional utilization of highly reactive organometallics. This method enables the efficient construction of the challenging chiral Csp<sup>3</sup>-C<sub>ArF</sub> bond with outstanding stereocontrol (up to 99% ee in most cases). This reaction proceeds under mild reaction conditions, demonstrating excellent functional group compatibility and high regio- and stereoselectivity. Experimental studies in conjunction with density functional theory (DFT) calculations were carried out to unravel the plausible mechanism and elucidate the origins of excellent enantioselectivity.

Chemical ScienceVol. 17(2)
Northeast Normal University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
Northeast Normal University, National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 73%
Catalytic C–H Functionalization Methods
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