Enabling Fluoroalkyl-Sulfonylalkylation and Fluoroalkyl-Halogenation of Alkenes and Alkynes via Photoredox Catalysis

2-type displacement. Notably, the same reaction condition can be extended to achieve iodo- and bromo-trifluoromethylation via a halogen atom transfer mechanism by utilizing alkyl iodides and bromoacetyl bromides, respectively, in place of general alkyl bromides.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-17
DOI
https://doi.org/10.1021/jacs.6c00567
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Enabling Fluoroalkyl-Sulfonylalkylation and Fluoroalkyl-Halogenation of Alkenes and Alkynes via Photoredox Catalysis

Supuni I. N. Hewa Inaththappulige, Harshvardhan Singh, Ayush Acharya, Nipuna D. D. Z. Agampodi
Journal of the American Chemical Society
Fluorine in Organic Chemistry
article

Enabling Fluoroalkyl-Sulfonylalkylation and Fluoroalkyl-Halogenation of Alkenes and Alkynes via Photoredox Catalysis

Supuni I. N. Hewa Inaththappulige, Harshvardhan Singh, Ayush Acharya, Nipuna D. D. Z. Agampodi
article en

Abstract

2-type displacement. Notably, the same reaction condition can be extended to achieve iodo- and bromo-trifluoromethylation via a halogen atom transfer mechanism by utilizing alkyl iodides and bromoacetyl bromides, respectively, in place of general alkyl bromides.

Journal of the American Chemical SocietyVol. 148(16)
Pennsylvania State University (US)
Pennsylvania State University, NIH Office of the Director, National Institute of General Medical Sciences
Clean water and sanitation
Openalex Percentile: Top 25%
Fluorine in Organic Chemistry
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