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- W4295398328 abstract "β-Amino carbonyl substructures are privileged motifs in natural products and active pharmaceutical compounds. Here, we report a photoinduced metal-free and highly regioselective intermolecular carboimination method via the simultaneous introduction of amino and carbonyl groups into the CC double bond in one step, providing straightforward, green and general access to both β-amino acid and β-amino ketone motifs from readily available alkene feedstocks. The mild reaction conditions, excellent functional group tolerance and product diversity should make this a broadly applicable carboimination approach of very broad interest to organic and medicinal chemists." @default.
- W4295398328 created "2022-09-13" @default.
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- W4295398328 date "2022-01-01" @default.
- W4295398328 modified "2023-10-18" @default.
- W4295398328 title "Metal-free photosensitized intermolecular carboimination of alkenes: a green and direct access to both β-amino acids and β-amino ketones" @default.
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- W4295398328 doi "https://doi.org/10.1039/d2ob01474b" @default.
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