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Abstract Herein, we report an electroreduction of unactivated alkyl alkenes enabled by Fe-H, which is provided through the combination of anodic iron salts and the silane generated in situ via cathodic reduction, using H 2 O as an H-source. The catalytic amounts of Si-additive work as an H-carrier from H 2 O to generate a highly active silane species in situ under continuous electrochemical conditions. This approach shows a broad substrate scope and good functional group compatibility. In addition to hydrogenation, the use of D 2 O instead of H 2 O provides the desired deuterated products in good yields with excellent D-incorporation (up to >99%). Further late-stage hydrogenation of complex molecules and drug derivatives demonstrate potential application in the pharmaceutical industry. Mechanistic studies are performed and provide support for the proposed mechanistic pathway.
Wang et al. (Sat,) studied this question.