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Diethylzinc-Mediated Radical 1,2-Addition of Alkenes and Alkynes.

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A novel diethylzinc-mediated radical 1,2-addition of perfluoroalkyl iodides to unactivated alkenes and alkynes is presented, which demonstrates a novel way to generate an ethyl difluoroacetate radical. This method is highly… Click to show full abstract

A novel diethylzinc-mediated radical 1,2-addition of perfluoroalkyl iodides to unactivated alkenes and alkynes is presented, which demonstrates a novel way to generate an ethyl difluoroacetate radical. This method is highly efficient and gives full conversions of the substrates, high yields of the products, and negligible byproducts and requires no column chromatography purifications. The mild conditions enable this protocol to exhibit excellent functional group compatibility.

Keywords: addition alkenes; diethylzinc mediated; mediated radical; radical addition; alkenes alkynes

Journal Title: Organic letters
Year Published: 2021

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