Indium (III) Acetate-Catalyzed Intermolecular Radical Addition of Organic Iodides to Electron-Deficient Alkenes
K Miura, M Tomita, J Ichikawa, A Hosomi
Index: Miura, Katsukiyo; Tomita, Mitsuru; Ichikawa, Junji; Hosomi, Akira Organic Letters, 2008 , vol. 10, # 1 p. 133 - 136
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Citation Number: 18
Abstract
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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