Stereoselective Synthesis of Monofluoroalkenes via Photoinduced Direct Monofluoroalkenylation of C(sp³)–H Bonds

Abstract In this study, a method is introduced for the photoinduced direct monofluoroalkenylation of C(sp³)–H bonds. A diverse range of fluoroacrylic acids react smoothly with various C–H substrates, leading to the formation of important monofluoroalkene motifs. Notably, this approach is cost-effective, exhibits high stereoselectivity, and eliminates the need for metal catalysts.

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Publication Details

Journal
Synlett
Published
2025-04-29
DOI
https://doi.org/10.1055/a-2596-9863
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Stereoselective Synthesis of Monofluoroalkenes via Photoinduced Direct Monofluoroalkenylation of C(sp³)–H Bonds

Wenjin Li, Xiaoyu Lu, Xiang Li, Haoyu Dong et al.
Synlett
Fluorine in Organic Chemistry
article

Stereoselective Synthesis of Monofluoroalkenes via Photoinduced Direct Monofluoroalkenylation of C(sp³)–H Bonds

Wenjin Li, Xiaoyu Lu, Xiang Li, Haoyu Dong, Xin-Ru Hu
article en

Abstract

Abstract In this study, a method is introduced for the photoinduced direct monofluoroalkenylation of C(sp³)–H bonds. A diverse range of fluoroacrylic acids react smoothly with various C–H substrates, leading to the formation of important monofluoroalkene motifs. Notably, this approach is cost-effective, exhibits high stereoselectivity, and eliminates the need for metal catalysts.

SynlettVol. 36(12)
Chuzhou University (CN)
Openalex Percentile: Top 93%
Fluorine in Organic Chemistry
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