Abstract
Allylation reactions, often used as a key step for constructing complex molecules and drug candidates, typically rely on transition-metal (TM) catalysts. Even though TM-free radical allylations have been developed using allyl-stannanes, -sulfides, -silanes or -sulfones, much less procedures have been reported using simple and commercially available allyl halides, that are used for the preparation of the before-mentioned allyl derivatives. Here, we present a straightforward photocatalytic protocol for the decarboxylative allylation of oxime esters using allyl bromide derivatives under metal-free and mild conditions. This methodology yields a diverse variety of functionalized molecules including several pharmaceutically relevant molecules.
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Geniller, L., Ben Kraim, H., Clot, E., Taillefer, M., Jaroschik, F., & Prieto, A. (2024). Metal-Free Decarboxylative Allylation of Oxime Esters under Light Irradiation. Chemistry - A European Journal, 30(43). https://doi.org/10.1002/chem.202401494
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