烯丙基重排
硅醇
亲核细胞
催化作用
化学
酒
有机化学
组合化学
药物化学
作者
Ken Motokura,Marika Ikeda,Minjune Kim,Kiyotaka Nakajima,Sae Kawashima,Masayuki Nambo,Wang‐Jae Chun,Shinji Tanaka
出处
期刊:Chemcatchem
[Wiley]
日期:2018-08-14
卷期号:10 (20): 4536-4544
被引量:18
标识
DOI:10.1002/cctc.201801097
摘要
Abstract Although allylation using allylic alcohol is an environmentally‐friendly method because of water being the sole byproduct in such reactions, allylic alcohol is one of the most difficult allylating agents in Pd‐catalyzed allylation of nucleophiles. In this study, we successfully developed a mesoporous silica‐supported Pd complex as an efficient catalyst for the allylation of nucleophiles using allylic alcohols as allylating agents. The allylic alcohol is activated by the silanol group on the support surface, which easily undergoes a π‐allylpalladium intermediate formation. The catalytic activity of the supported Pd complex was ca. 9 times higher than that of its homogeneous precursor Pd complex. A highest turnover number of 4500 based on Pd was achieved. Various nucleophiles and allylic alcohol derivatives could be used as substrates. Not only the detailed catalyst structure but also the reaction mechanism including the concerted activation of allylic alcohol by the Pd complex and silanol were investigated by several spectroscopic techniques, such as Pd K‐edge XAFS, solid‐state NMR, and in‐situ FT‐IR measurements.
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