Rational Design of a Second Generation Catalyst for Preparation of Allylsilanes Using the Silyl-Heck Reaction

被引:80
作者
McAtee, Jesse R. [1 ]
Yap, Glenn P. A. [1 ]
Watson, Donald A. [1 ]
机构
[1] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
基金
美国国家科学基金会;
关键词
NUCLEAR-MAGNETIC-RESONANCE; PHOSPHORUS LIGANDS; COUPLING REACTION; ARYLBORONIC ACIDS; TERMINAL OLEFINS; ALKENES; IODOTRIMETHYLSILANE; REAGENTS; ARYL; CHLOROSILANES;
D O I
10.1021/ja505446y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using rational ligand design, we have developed of a second-generation ligand, bis(3,5-di-tert-butylphenyl) (tert-butyl)phosphine, for the preparation of allylsilanes using the palladium-catalyzed silyl-Heck reaction. This new ligand provides nearly complete suppression of starting material alkene isomerization that was observed with our first-generation catalyst, providing vastly improved yields of allylsilanes from simple alkene starting materials. The studies quantifying the electronic and steric properties of the new ligand are described. Finally, we report an X-ray crystal structure of a palladium complex resulting from the oxidative addition of Me3SiI using an analogous ligand that provides significant insight into the nature of the catalytic system.
引用
收藏
页码:10166 / 10172
页数:7
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