A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds

被引:341
作者
Billingsley, Kelvin L. [1 ]
Anderson, Kevin W. [1 ]
Buchwald, Stephen L. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
关键词
amines; boronic acids; cross-coupling; heteroaryl halides; Suzuki-Miyaura reaction;
D O I
10.1002/anie.200600493
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Presented) Unprecedented activity: Catalysts derived from Pd and bulky dialkylphosphinobiaryl ligands are shown to be highly stable and active in Suzuki-Miyaura reactions of heteroaryl halides and heteroaryl boronic acids/esters (e.g., 3-or 4-pyridine, indole, and N-protected pyrrole derivatives). Furthermore, this catalyst system is not inhibited by the presence of highly basic aminopyridines or aminopyrimidines. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:3484 / 3488
页数:5
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