Hanna Steven, Wills Tyler, Butcher Trevor W, Hartwig John F
Division of Chemical Sciences, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States; Department of Chemistry, University of California, Berkeley, California 94708, United States.
Department of Chemistry, University of California, Berkeley, California 94708, United States.
ACS Catal. 2020 Aug 7;10(15):8736-8741. doi: 10.1021/acscatal.0c02697. Epub 2020 Jul 21.
We report a newly developed, palladium-catalyzed dehydrosilylation of terminal alkylsilanes that combines with chain-walking hydrosilylation to create a one-pot isomerization of internal olefins to terminal olefins. This catalytic dehydrosilylation is one of the few examples of thermal catalytic functionalizations of unactivated alkylsilanes. The reaction involves transmetalation of an alkylsilane, -hydride elimination, release of the terminal olefin, and reoxidation of the palladium catalyst. A variety of linear internal olefins underwent the overall isomerization to terminal olefins in good yields and in good regioselectivities. Particularly noteworthy, isomerizations occurring over seven carbon units proceeded in yields that are comparable to those of isomerizations occurring over one carbon unit.
我们报道了一种新开发的钯催化末端烷基硅烷的脱氢硅氢化反应,该反应与链行走氢化硅烷化反应相结合,可实现内烯烃到末端烯烃的一锅异构化反应。这种催化脱氢硅氢化反应是未活化烷基硅烷热催化官能团化的少数例子之一。该反应涉及烷基硅烷的金属转移、氢化物消除、末端烯烃的释放以及钯催化剂的再氧化。多种线性内烯烃以良好的产率和区域选择性进行了整体异构化反应生成末端烯烃。特别值得注意的是,跨越七个碳单元的异构化反应产率与跨越一个碳单元的异构化反应产率相当。