Metal‐Free Organophotocatalyzed Trifluoroethylation/Esterification of Alkenes

Abstract A metal‐free, organophotocatalyzed three‐component reaction between alkenes, 2,2,2‐trifluoroiodoethane, and carboxylic acids was developed. This protocol simultaneously introduces a trifluoroethyl group and an ester moiety in a single step. Preliminary mechanistic studies suggest the reaction proceeds via a radical pathway.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-10-18
DOI
https://doi.org/10.1002/ajoc.70232
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

Metal‐Free Organophotocatalyzed Trifluoroethylation/Esterification of Alkenes

Can Zeng, Xiangqing Zhang, Yao‐Fu Zeng, Yue Wang et al.
1 citations
Asian Journal of Organic Chemistry
Fluorine in Organic Chemistry
0.79
article

Metal‐Free Organophotocatalyzed Trifluoroethylation/Esterification of Alkenes

Can Zeng, Xiangqing Zhang, Yao‐Fu Zeng, Yue Wang, Fang Han
article en
1 citations

Abstract

Abstract A metal‐free, organophotocatalyzed three‐component reaction between alkenes, 2,2,2‐trifluoroiodoethane, and carboxylic acids was developed. This protocol simultaneously introduces a trifluoroethyl group and an ester moiety in a single step. Preliminary mechanistic studies suggest the reaction proceeds via a radical pathway.

Asian Journal of Organic ChemistryVol. 14(12)
Second People Hospital of Hunan (CN), University of South China (CN)
Openalex Percentile: Top 22%
Fluorine in Organic Chemistry
0.79
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Metal‐Free Organophotocatalyzed Trifluoroethylation/Esterification of Alkenes — Can Zeng, Xiangqing Zhang, et al. · Asian Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS