Vercruysse Sébastien, Cornelissen Loïc, Nahra Fady, Collard Laurent, Riant Olivier
Institute of Condensed Matter and Nanosciences-Molecules, Solids and Reactivity (IMCN/MOST), Université Catholique de Louvain, Place Louis Pasteur 1, bte L4.01.03, 1348 Louvain-la-Neuve (Belgium), Fax: (+32) 10 47-41-68.
Chemistry. 2014 Feb 10;20(7):1834-8. doi: 10.1002/chem.201304284. Epub 2014 Jan 21.
This paper describes a tunable and stereoselective dual catalytic system that uses copper and palladium reagents. This cooperative silylcupration and palladium-catalyzed allylation readily affords trisubstituted alkenylsilanes. Fine-tuning the reaction conditions allows selective access to one stereoisomer over the other. This new methodology tolerates different substituents on both coupling partners with high levels of stereoselectivity. The one-pot reaction involving a Cu(I)/Pd(0) cooperative dual catalyst directly addresses the need to develop more time-efficient and less-wasteful synthetic pathways.
本文描述了一种使用铜和钯试剂的可调谐且具有立体选择性的双催化体系。这种协同的硅氢化铜化反应和钯催化的烯丙基化反应能够轻松地得到三取代的烯基硅烷。微调反应条件可选择性地获得一种立体异构体而非另一种。这种新方法在两个偶联伙伴上都能容忍不同的取代基,且具有高度的立体选择性。涉及Cu(I)/Pd(0)协同双催化剂的一锅法反应直接满足了开发更省时且浪费更少的合成途径的需求。