Organometallic Chemistry Laboratory and RIKEN Center for Sustainable Resource Science, RIKEN , 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
J Am Chem Soc. 2016 Mar 23;138(11):3663-6. doi: 10.1021/jacs.6b01349. Epub 2016 Mar 10.
Metal-free catalytic C-H silylation of a series of aromatic compounds such as N,N-disubstituted anilines with various hydrosilanes has been achieved for the first time using commercially available B(C6F5)3 as a catalyst. This protocol features simple and neutral reaction conditions, high regioselectivity, wide substrate scope (up to 40 examples), Si-Cl bond compatibility, and no requirement for a hydrogen acceptor.
首次使用商业可得的 B(C6F5)3 作为催化剂,实现了一系列芳香族化合物(如 N,N-二取代苯胺)与各种硅烷的无金属催化 C-H 硅烷化。该方法具有反应条件简单、中性、高区域选择性、广泛的底物范围(多达 40 个实例)、Si-Cl 键兼容性以及不需要氢受体等优点。