Yang Liqun, Yi Mingjun, Wu Xiaoyu, Lu Yan, Zhang Zhaoguo
Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, China.
Chemistry. 2024 Nov 15;30(64):e202402406. doi: 10.1002/chem.202402406. Epub 2024 Oct 30.
A concise hydrosilylation of alkynes for synthesizing β-(E)-vinylsilanes catalyzed by dirhodium(II)/XantPhos has been developed. In this reaction, β-(E)-vinylsilanes were generated from the isomerization of β-(Z)-vinylsilanes catalyzed by dirhodium(II) hydride species rather than the direct insertion of triple bond into M-H or M-Si bond (traditional Chalk-Harrod mechanism or modified Chalk-Harrod mechanism). The hydrosilylation displayed a broad substrate scope for alkynes and tertiary silanes, tolerating diverse functional groups including halides, nitriles, amines, esters, and heterocycles.
已开发出一种由二铑(II)/XantPhos催化的用于合成β-(E)-乙烯基硅烷的炔烃简洁硅氢化反应。在该反应中,β-(E)-乙烯基硅烷是由氢化二铑(II)物种催化的β-(Z)-乙烯基硅烷异构化产生的,而不是通过三键直接插入M-H或M-Si键(传统的查尔-哈罗德机理或改进的查尔-哈罗德机理)。该硅氢化反应对炔烃和叔硅烷显示出广泛的底物范围,能够耐受包括卤化物、腈、胺、酯和杂环在内的各种官能团。