341022-97-7Relevant articles and documents
Palladium-catalyzed synthesis of diarylbenzenes from coupling reactions between equal amount of diiodoarenes and arylboronic acids
Mao, Jincheng,Li, Ran,He, Yue,Yang, Xiaojiang,Wang, Dingli,Zhang, Yang
, p. 663 - 669 (2016/07/26)
We reported a highly effective Pd-catalytic system for the synthesis of diarylbenzenes through Suzuki-type reaction between equal amount of diiodoarenes and arylboronic acids. This preferential oxidative addition resulted in such high selectivity.
Highly efficient cyclopalladated ferrocenylimine catalyst for Suzuki cross-coupling reaction of 3-pyridylboronic pinacol ester with aryl halides
Zhang, Jinli,Zhao, Liang,Song, Maoping,Mak, Thomas C.W.,Wu, Yangjie
, p. 1301 - 1306 (2007/10/03)
The Suzuki cross-coupling reaction of 3-pyridylboronic pinacol ester with aryl iodides, bromides and chlorides was carried out in DMF/H2O (3/1, v/v) at 110 °C in the presence of cyclopalladated ferrocenylimine I and K2CO3 or CsCO3 (1.0 equiv.) without the protection of inert gas. By using this method the synthesis of 3-pyridyl biaryl compounds could be readily achieved.