期刊
CHEMICAL SCIENCE
卷 10, 期 19, 页码 5079-5084出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8sc05391j
关键词
-
资金
- Royal Society
- Syngenta
- University of Edinburgh, School of Chemistry
The widespread adoption of earth-abundant metal catalysis lags behind that of the second-and third-row transition metals due to the often challenging practical requirements needed to generate the active low oxidation-state catalysts. Here we report the development of a single endogenous activation protocol across five reaction classes using both iron-and cobalt pre-catalysts. This simple catalytic manifold uses commercially available, bench-stable iron-or cobalt tetrafluoroborate salts to perform regiodivergent alkene and alkyne hydrosilylation, 1,3-diene hydrosilylation, hydrogenation, [ 2p + 2p]-cycloaddition and C-H borylation. The activation protocol proceeds by fluoride dissociation from the counterion, in situ formation of a hydridic activator and generation of a low oxidation-state catalyst.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据