期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2012, 期 3, 页码 595-603出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201101409
关键词
Cross-coupling; Halides; Borylation; Palladium; Biaryls
资金
- National Natural Science Foundation of China (NSFC) [20972139]
- National Science Foundation (NSF) of Henan [082300423201]
The tricyclohexylphosphane adduct of cyclopalladated ferrocenylimine I exhibited high catalytic activity in the one-pot borylation/Suzuki-Miyaura coupling (BSC) reaction with low catalyst loading (2 mol-%). Various biaryls were obtained in good to excellent yields for 37 examples. This process was applied to aryl and heteroaryl halides (Br and Cl) containing a variety of functional groups and did not require an excess amount of phosphane ligand and the addition of the palladium catalyst in the second step.
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