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Visible-light-mediated allylation of alkyl radicals with allylic sulfones via a deaminative strategy

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Abstract

A visible-light-mediated radical allylation of primary amine-derived Katritzky salts with allylic sulfones via C(sp3)–N bond activation is reported, furnishing the corresponding alkenes in satisfactory yields. This mild protocol provides an efficient strategy for site-specific C(sp3)–C(sp3) bond formation using abundant feedstock primary amines, particularly α-amino acids as alkyl radical precursors. This photocatalytic reaction demonstrates a broad substrate scope and good functional group tolerance.

Graphical abstract: Visible-light-mediated allylation of alkyl radicals with allylic sulfones via a deaminative strategy

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Publication details

The article was received on 28 Sep 2018, accepted on 18 Oct 2018 and first published on 19 Oct 2018


Article type: Research Article
DOI: 10.1039/C8QO01046C
Citation: Org. Chem. Front., 2018, Advance Article
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    Visible-light-mediated allylation of alkyl radicals with allylic sulfones via a deaminative strategy

    M. Zhang and F. Liu, Org. Chem. Front., 2018, Advance Article , DOI: 10.1039/C8QO01046C

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