Palladium(0)-Catalyzed Silylation of Aryl Halides with Triorganosilanes: Synthesis of Aryl(2-furyl)silanes

Palladium(0)-Catalyzed Silylation of Aryl Halides with Triorganosilanes: Synthesis of Aryl(2-furyl)silanes
复制标题

DOI：
10.1055/s-2006-942368
复制
发表时间：
2006-06
期刊：
Synthesis
影响因子：
--
通讯作者：
Miki Murata;Hiroya Ohara;R. Oiwa;Shinji Watanabe;Y. Masuda
Miki Murata;Hiroya Ohara;R. Oiwa;Shinji Watanabe;Y. Masuda
中科院分区：
其他
文献类型：
--
作者：
Miki Murata;Hiroya Ohara;R. Oiwa;Shinji Watanabe;Y. Masuda

文献摘要

相似文献

三有机硅烷在硅原子上有两个芳基，在钯催化下进行芳基碘的硅烷化反应。得到的芳基(2-呋喃)硅烷在过渡金属催化剂和四丁基氟化铵存在下，可作为碳-碳键形成反应的起始原料。
Triorganosilanes, which possess two aryl groups on the silicon atom, undergo palladium-catalyzed silylation of aryl iodides. Aryl(2-furyl)silanes thus obtained are potentially useful starting materials for carbon-carbon bond-forming reactions in the presence of transition-metal catalysts and tetrabutylammonium fluoride.