Light‐Induced Radical C(sp2)−H Trifluorovinylation of (Hetero)arenes with a Trifluorovinyl Iodine(III) Reagent (TrFVI)
Year: 2025
Type: article
Abstract: Trifluorovinyl group is an emerging and valuable motif in drug discovery and material science, especially in polymer‐related researches. However, the practical and efficient synthesis of trifluorovinylated compounds with broad structural diversity still remains a challenging task. Herein, we report the scalable synthesis of a trifluorovinyl hypervalent iodine(III) reagent, ArI(CF ═ CF2)OTf (TrFVI), from a bulk chemical, HFC‐134a. The first C(sp2)─H trifluorovinylation of (hetero)arenes is achieved using TrFVI reagent via photoredox catalysis, which shows good functional group compatibility. Furthermore, late‐stage trifluorovinylation of highly modified substrates, including drug candidates, is achieved to illustrate the powerfulness of our method. A possible radical pathway is proposed according to the mechanism study.
Authors: Fei Wang, Ruitong Zhang, Xiangyu Chen, Yingqi Han, Zongchang Han, Yunchen Jiang, Yaxing Wu, Boyu Shi, Chao Chen
Institution: Tsinghua University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: bronze
Award: 可后修饰二氟乙基高价碘试剂的设计合成与反应性质研究
OpenAlex ID: W4413106822
