Chemoselective and fast decarboxylative allylation by photoredox catalysis under mild conditions

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Abstract

Here we report a visible-light-induced decarboxylative allylation to build C(sp3)-allyl bonds. This allylation reaction works for primary, secondary, tertiary, benzyl, and alpha-heteroatom-substituted alkyl N-acyloxyphthalimides and is compatible with many sensitive functional groups. The reaction is complete in minutes at room temperature and can be run in both organic solvents and neutral aqueous solutions. A series of mechanistic experiments have been implemented and a functional-group-rich oligosaccharide modification is demonstrated with the decarboxylative allylation.

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Hu, C., & Chen, Y. (2015). Chemoselective and fast decarboxylative allylation by photoredox catalysis under mild conditions. Organic Chemistry Frontiers, 2(10), 1352–1355. https://doi.org/10.1039/c5qo00187k

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