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Indium(III) acetate-catalyzed intermolecular radical addition of organic iodides to electron-deficient alkenes.

Organic letters (2007-12-13)
Katsukiyo Miura, Mitsuru Tomita, Junji Ichikawa, Akira Hosomi
RESUMEN

In the presence of phenylsilane and a catalytic amount of indium(III) acetate, organic iodides added to electron-deficient alkenes in ethanol at room temperature. Both simple and functionalized organic iodides were applicable to this reaction. A plausible reaction mechanism involves the formation of indium hydride species by hydride transfer from silicon to indium and an indium hydride-mediated radical chain process.

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Indium(III) acetate, 99.99% trace metals basis