Mechanistic Investigation of the Palladium-Catalyzed Synthesis of Allylic Silanes and Boronates from Allylic Alcohols

被引:73
作者
Larsson, Johanna M. [1 ]
Szabo, Kalman J. [1 ]
机构
[1] Stockholm Univ, Dept Organ Chem, SE-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
OPTICALLY-ACTIVE ALLYLSILANES; CROSS-COUPLING REACTIONS; (PI-ALLYL)PALLADIUM COMPLEXES; ALLYLATION; SUBSTITUTION; ACTIVATION; ACID; ISOMERIZATION; SILYLATION; METAL;
D O I
10.1021/ja309860h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The mechanism of the palladium-catalyzed synthesis of allylic silanes and boronates from allylic alcohols was investigated. H-1, Si-29, F-19, and B-11 NMR spectroscopy was used to reveal key intermediates and byproducts of the silylation reaction. The tetrafluoroborate counterion of the palladium catalyst is proposed to play an important role in both catalyst activation as well as the transmetalation step. We propose that BF3 is generated in both processes and is responsible for the activation of the substrate hydroxyl group. An (eta(3)-allyl)palladium complex has been identified as the catalyst resting state, and the formation of (eta(3)-allyl)palladium complexes directly from allylic alcohols has been studied. Kinetic analysis provides evidence that the turnover limiting step is the transmetalation, and insights into notable similarities between the borylation and the silylation reaction mechanisms enabled us to considerably improve the stereoselectivity of the borylation.
引用
收藏
页码:443 / 455
页数:13
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