Fe(III)-catalyzed decarboxylation achieves regioselective fluoroalkylation in unactivated alkenes, suggesting broad application potential.
The difunctionalization of unactivated alkenes represents a powerful strategy for constructing complex molecular architectures. Herein, we report a light-induced Fe(III)-catalyzed decarboxylation strategy for the regioselective migratory difunctionalization of distal unactivated alkenes using cost-effective and readily accessible fluoroalkyl carboxylic acids as fluoroalkyl radical precursors. This approach features the generality of the migration groups, including aryl, heteroaryl, cyano, and alkynyl groups and successful incorporation of mono-, di-, tri-, and perfluoroalkyl moieties.
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Zhong et al. (2025) studied this question.
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