Hydrosilylation of alkynes by Ni(CO)3-stabilized silicon(II) hydride.

Hydrosilylation of alkynes by Ni(CO)3-stabilized silicon(II) hydride.
复制标题

DOI:
10.1002/anie.201105722
复制
发表时间:
2012-01
期刊:
影响因子:
--
通讯作者:
Miriam Stoelzel;C. Präsang;S. Inoue;Stephan Enthaler;M. Driess
Miriam Stoelzel;C. Präsang;S. Inoue;Stephan Enthaler;M. Driess
中科院分区:
--
文献类型:
--
作者:
Miriam Stoelzel;C. Präsang;S. Inoue;Stephan Enthaler;M. Driess

文献摘要

被引文献

相似文献

不可复制粘贴:虽然β-双酮配体已被用于稳定Ge(II)和Sn(II)氢化物,但相应的Si(II)氢化物是不可接近的。然而,硅(II)与{Ni(CO)(3)}片段的配位使得第一个Si(II)氢化物金属配合物1得以分离。该配合物首次用于硅(II)基和Ni(0)介导的烷基立体选择性硅氢化反应。R =苯基,甲苯。
Not copy and paste: Although β-diketiminato ligands have been employed for the stabilization of Ge(II) and Sn(II) hydrides, the corresponding Si(II) hydride is not accessible. However, coordination of silicon(II) to a {Ni(CO)(3)} fragment allowed the isolation of the first Si(II) hydride metal complex 1. This complex was used for the first silicon(II)-based and Ni(0)-mediated, stereoselective hydrosilylation of alkynes. R = phenyl, tolyl.