硅烷
电化学
组合化学
催化作用
化学
过氧化氢
阴极保护
分子
阳极
基质(水族馆)
氘
烷基
原位
氢
功能群
有机化学
电极
物理化学
聚合物
地质学
物理
海洋学
量子力学
作者
Yanwei Wang,Qian Wang,Lei Wu,Kangping Jia,Minyan Wang,Youai Qiu
标识
DOI:10.1038/s41467-024-47168-w
摘要
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.
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