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通过立体特异性碳-碳键裂解实现铁催化的乙烯基环丙烷的不对称硅氢化反应

Iron-Catalyzed Asymmetric Hydrosilylation of Vinylcyclopropanes via Stereospecific C-C Bond Cleavage.

作者信息

Chen Chenhui, Wang Hongliang, Sun Yufeng, Cui Jiayan, Xie Jianbo, Shi Yang, Yu Shijia, Hong Xin, Lu Zhan

机构信息

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310058, China.

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310058, China.

出版信息

iScience. 2020 Apr 24;23(4):100985. doi: 10.1016/j.isci.2020.100985. Epub 2020 Mar 17.

Abstract

An iron-catalyzed highly anti-Markovnikov selective, enantioselective hydrosilylation of vinylcyclopropanes with PhSiH was reported for the preparation of valuable chiral allylic silanes via stereospecific C-C bond cleavage. Simultaneously, difficultly prepared chiral VCPs could be also obtained with moderate to excellent enantioselectivity via this kinetic resolution pathway. The chiral Z-allylic silanes could be converted to various chiral allylic derivatives. A possible mechanism via an iron-silyl species was proposed based on experimental and computational studies.

摘要

据报道,通过立体特异性C-C键裂解制备有价值的手性烯丙基硅烷时,铁催化乙烯基环丙烷与PhSiH发生高度反马氏选择性、对映选择性硅氢化反应。同时,通过这种动力学拆分途径,也可以以中等至优异的对映选择性获得难以制备的手性乙烯基环丙烷。手性Z-烯丙基硅烷可以转化为各种手性烯丙基衍生物。基于实验和计算研究,提出了一种通过铁硅烷基物种的可能机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/958b/7115165/b3855c0be69a/fx1.jpg

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