Trifluoromethanesulfinyl chloride: an effective trifluoromethyl radical source in the trifluoromethylimination of alkenes

CF 3 SOCl as CF 3 source to achieve catalyst-free, highly regioselective intermolecular trifluoromethylimination of alkenes towards β-trifluoromethylamines.

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Publication Details

Journal
Green Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5gc01651g
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Trifluoromethanesulfinyl chloride: an effective trifluoromethyl radical source in the trifluoromethylimination of alkenes

Jiayu Liang, Weilong Lin, Shuping Wang, Xingda Zhao
Green Chemistry
Fluorine in Organic Chemistry
article

Trifluoromethanesulfinyl chloride: an effective trifluoromethyl radical source in the trifluoromethylimination of alkenes

Jiayu Liang, Weilong Lin, Shuping Wang, Xingda Zhao
article en

Abstract

CF 3 SOCl as CF 3 source to achieve catalyst-free, highly regioselective intermolecular trifluoromethylimination of alkenes towards β-trifluoromethylamines.

Green ChemistryVol. 27(31)
Shenzhen University (CN), Shenzhen Maternity and Child Healthcare Hospital (CN)
Openalex Percentile: Top 87%
Fluorine in Organic Chemistry
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Trifluoromethanesulfinyl chloride: an effective trifluoromethyl radical source in the trifluoromethylimination of alkenes — Jiayu Liang, Weilong Lin, et al. · Green Chemistry (2025) | TGRS Research Map | TGRS