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Visible-light-initiated catalyst-free trifluoromethylselenolation of arylsulfonium salts with [Me<sub>4</sub>N][SeCF<sub>3</sub>]

Zeyu Tian, Cheng‐Pan Zhang

2022Organic Chemistry Frontiers46 citationsDOI

Abstract

Catalyst-free visible-light irradiation has leveraged the big redox potential gaps between arylsulfonium salts and [Me 4 N][SeCF 3 ], which combined with sulfenylation processes offers convenient and selective C–H trifluoromethylselenolation.

Topics & Concepts

ChemistryCatalysisVisible spectrumRedoxIrradiationPhotochemistryCombinatorial chemistryInorganic chemistryOrganic chemistryOptoelectronicsNuclear physicsPhysicsFluorine in Organic ChemistrySulfur-Based Synthesis TechniquesRadical Photochemical Reactions
Visible-light-initiated catalyst-free trifluoromethylselenolation of arylsulfonium salts with [Me<sub>4</sub>N][SeCF<sub>3</sub>] | Litcius