Cover Feature: Fluoroalkyl Sulfoximines for Versatile Photocatalytic Radical Fluoroalkylations (Chem. Rec. 9/2023) |
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Authors: | Prof. Dr. Takashi Koike |
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Affiliation: | Department of Applied Chemistry, Faculty of Fundamental Engineering Nippon Institute of Technology E24-315, 4–1 Gakuendai, Miyashiro-Machi, Minamisaitama-gun, Saitama, 345-8501 Japan |
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Abstract: | Fluoroalkyl sulfoximines, which serve as electron-accepting fluoroalkyl radical sources, are easy-to-handle, solid, and bench-stable chemicals. Fluoroalkyl radicals can be generated from sulfoximine reagents using strong one-electron injectors, such as a highly reducing photoredox catalyst in the excited state. Our group has developed photocatalytic radical di- and mono-fluoromethylation and α-monofluoroalkylation of olefins with the corresponding fluoroalkyl sulfoximines. In this personal account, appropriate combinations of fluoroalkyl sulfoximines and photoredox catalysts, leading to successful radical fluoroalkylation, have been discussed. |
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Keywords: | fluorine photocatalysis radical reaction electron transfer sulfoximine |
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