Metallaphotoredox-enabled enantioselective aryldifluoromethyl-alkynylation of alkenes <i>via</i> C(sp<sup>3</sup>)–F bond activation

Enantioselective aryldifluoromethyl-alkynylation of alkenes through C(sp 3 )–F bond activation of ArCF 3 via photoredox/copper catalysis has been reported for the first time. Various products were synthesized with high yields and enantioselectivities.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00370a
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

Metallaphotoredox-enabled enantioselective aryldifluoromethyl-alkynylation of alkenes via C(sp3)–F bond activation

Zhanyong Tang, Xiaoqiang Ma, Jiasheng Huang, Xiaojing Zhao et al.
1 citations
Organic Chemistry Frontiers
Fluorine in Organic Chemistry
0.79
article

Metallaphotoredox-enabled enantioselective aryldifluoromethyl-alkynylation of alkenes via C(sp3)–F bond activation

Zhanyong Tang, Xiaoqiang Ma, Jiasheng Huang, Xiaojing Zhao, Depeng Zhao, Xingda Zhao, Liying Fu
article en
1 citations

Abstract

Enantioselective aryldifluoromethyl-alkynylation of alkenes through C(sp 3 )–F bond activation of ArCF 3 via photoredox/copper catalysis has been reported for the first time. Various products were synthesized with high yields and enantioselectivities.

Organic Chemistry FrontiersVol. 12(14)
Sun Yat-sen University (CN)
Openalex Percentile: Top 30%
Fluorine in Organic Chemistry
0.79
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