scholarly journals Efficient Stille Cross-Coupling Reaction Catalyzed by the Pd(OAc)2/Dabco Catalytic System.

ChemInform ◽  
2005 ◽  
Vol 36 (34) ◽  
Author(s):  
Jin-Heng Li ◽  
Yun Liang ◽  
De-Ping Wang ◽  
Wen-Jie Liu ◽  
Ye-Xiang Xie ◽  
...  
Author(s):  
Yuto Seo ◽  
Wahyu S. Putro ◽  
Miftah Faried ◽  
Vladimir Ya. Lee ◽  
Tomoteru Mizusaki ◽  
...  

2017 ◽  
Vol 15 (27) ◽  
pp. 5805-5810 ◽  
Author(s):  
Yan Liu ◽  
Jia Yuan ◽  
Zi-Fei Wang ◽  
Si-Hao Zeng ◽  
Meng-Yue Gao ◽  
...  

An efficient solvent-free and aqueous protocol for the Buchwald–Hartwig cross-coupling reaction has been developed. Notably, the catalytic system also efficiently catalyzed the reaction under aqueous conditions.


Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 86 ◽  
Author(s):  
Xiaogang Li ◽  
Wenbin Zhang ◽  
Leiqing Fu ◽  
Mengping Guo

In this study, a convenient and highly efficient catalytic system for the Suzuki-Miyaura coupling reaction was investigated under mild conditions. A combination of Pd(CH3CN)2Cl2 and pipecolinic acid showed excellent catalytic performance and afforded high turnover numbers; turnover numbers were up to 4.9 × 105 for the coupling reaction of 4-bromobenzoic acid and tetraphenylboron sodium. The catalytic system was also effective for the indexes of 4-bromobenzoic acid, and high turnover numbers were obtained.


ChemInform ◽  
2012 ◽  
Vol 43 (10) ◽  
pp. no-no
Author(s):  
Gong Chen ◽  
Jianwei Xie ◽  
Jiang Weng ◽  
Xinhai Zhu ◽  
Zhanchao Zheng ◽  
...  

Tetrahedron ◽  
2005 ◽  
Vol 61 (30) ◽  
pp. 7289-7293 ◽  
Author(s):  
Jin-Heng Li ◽  
Yun Liang ◽  
Ye-Xiang Xie

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