Highly Efficient Cyclopalladated Ferrocenylimine Catalyst for Suzuki Cross-Coupling Reaction of 3-Pyridylboronic Pinacol Ester with Aryl Halides.

ChemInform ◽  
2006 ◽  
Vol 37 (28) ◽  
Author(s):  
Jinli Zhang ◽  
Liang Zhao ◽  
Maoping Song ◽  
Thomas C. W. Mak ◽  
Yangjie Wu
2016 ◽  
Vol 14 (20) ◽  
pp. 4664-4668 ◽  
Author(s):  
Yan Liu ◽  
Hui Peng ◽  
Jia Yuan ◽  
Meng-Qi Yan ◽  
Xue Luo ◽  
...  

An air-stable aryl substituted indenyl phosphine used in combination with Pd(OAc)2 provides a highly efficient catalyst for the Suzuki–Miyaura cross-coupling reaction of sterically hindered aryl halides with aryl boronic acids.


ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Anns Maria Thomas ◽  
Sujatha Asha ◽  
K. S.. Sindhu ◽  
Gopinathan Anilkumar

2020 ◽  
Vol 56 (74) ◽  
pp. 10942-10945
Author(s):  
Yichao Gu ◽  
Xueliang Sun ◽  
Bin Wan ◽  
Zhuoer Lu ◽  
Yanghui Zhang

A palladium-catalyzed cross-coupling reaction of aryl halides with 2-chlorobenzoic acids has been developed through C(sp3)–H activation, which provides an innovative method for the synthesis of 9,10-dihydrophenanthren.


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