Homolytic N−S Bond Cleavage in Vinyl Triflimides Enabled by Triplet–Triplet Energy Transfer

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Abstract

Vinyl triflimides are a new compound class with unknown reactivity. A computational analysis identified homolytic cleavage of the N−Tf bond induced by triplet–triplet energy transfer (EnT) as a highly interesting reaction type that might be accessible. A combination of experimental and mechanistic work verified this hypothesis and proved the generated radicals to be amenable to radical–radical coupling. Thereby, vinyl triflimides were transformed into a range of α-quaternary, β-trifluoromethylated amines in a 1,2-difunctionalization reaction with no need for external CF3 reagents.

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Strauch, C., Schroeder, S., Grelier, G., & Niggemann, M. (2022). Homolytic N−S Bond Cleavage in Vinyl Triflimides Enabled by Triplet–Triplet Energy Transfer. Chemistry - A European Journal, 28(53). https://doi.org/10.1002/chem.202201830

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