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作 者:程彪 陆鹏 赵家金 陆展[1] Cheng Biao;Lu Peng;Zhao Jiajin;Lu Zhan(Department of Chemistry,Zhejiang University,Hangzhou 310058)
机构地区:[1]浙江大学化学系
出 处:《有机化学》2019年第6期1704-1710,共7页Chinese Journal of Organic Chemistry
基 金:Project supported by the National Natural Science Foundation of China(No.21772171);the National Basic Research Program of China(973 Program,No.2015CB856600);the Zhejiang Provincial Natural Science Foundation(No.LR19B020001);the K.P.Chao’s High Technology Development Foundation of Zhejiang University and the Fundamental Research Funds for the Central Universities~~
摘 要:描述了一种钴催化的高化学、区域、立体选择性的芳香族烯烃的脱氢硅化反应.亚胺吡啶咪唑啉的钴络合物可以有效促进该反应,并能显著提高该反应的化学选择性.该方法利用地球丰产过渡金属、廉价易得的烯烃和硅烷来构建具有高附加值的烯基硅烷.文中同时描述了该反应可放大到克级规模制备及可能的反应机理.A highly chemo-,regio-,and stereo-selective cobalt-catalyzed dehydrogenative silylation of vinylarenes was described.The imidazoline iminopyridine cobalt complex could promote this reaction effectively and improve the chemoselectivity dramatically.This protocol used earth-abundant transition metal,readily available alkenes and hydrosilanes to construct valuable vinylsilanes.The reaction could be carried out in gramscale and the proposed mechanism was also described.
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