Activation of the P-H bond by a frustrated Lewis pair and its application in catalytic Z-selective hydrophosphonylation of terminal ynones

被引:11
作者
Liu, Yizhen [1 ]
Fan, Xiaoting [1 ]
Li, Zhen Hua [1 ]
Wang, Huadong [1 ]
机构
[1] Fudan Univ, Dept Shanghai Key Lab Mol Catalysis & Innovat Mat, Dept Chem, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
ACID/BRONSTED BASE CATALYSTS; FREE HYDROGEN ACTIVATION; CHEMISTRY; ACID;
D O I
10.1039/c7cc05028c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The frustrated Lewis pair (FLP) comprised of B(C6F5)(3) and 1,2,2,6,6-pentamethylpiperidine (PMP) can efficiently catalyze Z-selective hydrophosphonylation of terminal ynones with a Z/E selectivity of up to 20 :1. Mechanistic studies suggest that the trans arrangement of the phosphite nucleophilic attack and hydrogen bond formation on the alkyne moiety is responsible for the observed Z-selectivity.
引用
收藏
页码:10890 / 10893
页数:4
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