化学选择性
催化作用
化学
硅烷化
药物化学
反应条件
有机化学
作者
Zubao Gan,De-Yun Cui,Hongyun Zhang,Ying Feng,Liying Huang,Yingying Gui,Gao L,Zhenlei Song
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2022-07-24
卷期号:27 (15): 4730-4730
被引量:2
标识
DOI:10.3390/molecules27154730
摘要
(Ph3C)[BPh(F)4]-catalyzed Hosomi-Sakurai allylation of allylsilanes with β,γ-unsaturated α-ketoesters has been developed to give γ,γ-disubstituted α-ketoesters in high yields with excellent chemoselectivity. Preliminary mechanistic studies suggest that trityl cation dominates the catalysis, while the silyl cation plays a minor role.
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