Scholay

学术搜索 · AI 审稿 · LaTeX 协作

Harnessing Electrochemistry for Direct Deoxygenative Silylation of Alcohols and Ketones

作者:Yanping Zheng, Yuanxin Wu, Liping Su, Peng Xiong, Hai‐Chao Xu · 发表于:Angewandte Chemie International Edition · 年份:2025 · DOI:10.1002/anie.202509411 · 被引用次数:12 · 研究领域:Chemical Synthesis and Reactions、Fuel Cells and Related Materials、Electrochemical Analysis and Applications

Alcohols and ketones are abundant and structurally diverse feedstocks, yet their direct transformation into organosilicon compounds remains challenging due to the difficulty in selective cleaving C─OH and C═O bonds. Here, we report an electrochemically driven deoxygenative C─Si bond formation strategy that converts alcohols and ketones directly to organosilicon compounds. The reactions operate under mild conditions without external redox reagents and sacrificial electrodes. A wide range of alcohols, including primary, secondary, and tertiary alcohols, as well as ketones, are efficiently converted to the corresponding organosilane products. Overall, this study provides a step-economical, highly efficient, and synthetically versatile platform for the direct conversion of feedstock chemicals into valuable organosilicon compounds.