A highly efficient catalyst of a nitrogen-based ligand for the Suzuki coupling reaction at room temperature under air in neat water

2014 ◽  
Vol 12 (25) ◽  
pp. 4511-4516 ◽  
Author(s):  
Shiwen Liu ◽  
Meiyun Lv ◽  
Daoan Xiao ◽  
Xiaogang Li ◽  
Xiuling Zhou ◽  
...  

Glycine is used to prepare an air-stable and water-soluble catalyst for the Suzuki–Miyaura reaction. In the presence of 0.1% [PdCl2(NH2CH2COOH)2], excellent catalytic activity is observed at room temperature under air in neat water.

RSC Advances ◽  
2015 ◽  
Vol 5 (61) ◽  
pp. 49568-49576 ◽  
Author(s):  
Mohammad Gholinejad ◽  
Mehran Razeghi ◽  
Carmen Najera

Magnetic nanoparticles of Fe3O4 supported oxime palladacycle as a novel catalyst for room temperature Suzuki coupling reaction in aqueous media.


ChemInform ◽  
2005 ◽  
Vol 36 (38) ◽  
Author(s):  
Jun-xiao Yang ◽  
Kuo-yan Ma ◽  
Fang-hua Zhu ◽  
Wen Chen ◽  
Bo Li ◽  
...  

2014 ◽  
Vol 2 (44) ◽  
pp. 18952-18958 ◽  
Author(s):  
Mitasree Maity ◽  
Uday Maitra

Palladium nanoparticles were efficiently prepared in situ by sodium cyanoborohydride reduction of Pd(ii) at room temperature using calcium-cholate hydrogel fibers as templates. The PdNPs self-organize on the gel fibers, which supports the controlled growth as well as stabilization of PdNPs. The hybrid xerogel was used as an efficient catalyst for the Suzuki coupling reaction in water.


2019 ◽  
Vol 6 (3) ◽  
pp. 352-361 ◽  
Author(s):  
Guangyang Bao ◽  
Jie Bai ◽  
Chunping Li

A novel Pd1Ni4 bimetal nanocomposite catalyst was prepared and showed better performance than their monometallic counterpart. What's more, the catalyst could be reused ten times without significant change in catalytic activity, which met the request of sustainable chemistry.


RSC Advances ◽  
2014 ◽  
Vol 4 (69) ◽  
pp. 36437-36443 ◽  
Author(s):  
Zhenhong Guan ◽  
Buyi Li ◽  
Guoliang Hai ◽  
Xinjia Yang ◽  
Tao Li ◽  
...  

Microporous polymers with built-in triphenylphosphine palladium exhibit highly efficient catalytic activity for cross-coupling reactions of benzyl chloride under mild conditions.


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