ChemInform Abstract: Evaluation of Catalytic Activity of Copper Salts and Their Removal Processes in the Three-Component Coupling Reactions

ChemInform ◽  
2008 ◽  
Vol 39 (43) ◽  
Author(s):  
Seung Jun Hwang ◽  
Seung Hwan Cho ◽  
Sukbok Chang
Keyword(s):  
Catalytic Activity ◽  
Coupling Reactions ◽  
Copper Salts ◽  
Removal Processes ◽  
Three Component Coupling

Evaluation of catalytic activity of copper salts and their removal processes in the three-component coupling reactions

2008 ◽  
Vol 80 (5) ◽  
pp. 873-879 ◽  
Author(s):  
Seung Jun Hwang ◽  
Seung Hwan Cho ◽  
Sukbok Chang
Keyword(s):  
Catalytic Activity ◽  
Coupling Reaction ◽  
Coupling Reactions ◽  
Terminal Alkynes ◽  
Ligand Effect ◽  
Copper Salts ◽  
Wide Range ◽  
Sulfonyl Azides ◽  
Removal Processes ◽  
Three Component Coupling

The catalytic activity of a wide range of copper salts, including Cu(I) and Cu(II), has been examined in the Cu-catalyzed three-component coupling reactions of sulfonyl azides, terminal alkynes, and amines, alcohols, or water to afford N-sulfonyl amidines, imidates, and amides, respectively. Furthermore, the investigation on the ligand effect in our protocol has revealed that certain types of ligands such as tris(benzyltriazolylmethyl)amine (TBTA) exhibited notable acceleration effects on the coupling reaction. The facile and efficient methods for removing copper salts from reaction mixture were also examined.

scholarly journals Magnetization of graphene oxide nanosheets using nickel magnetic nanoparticles as a novel support for the fabrication of copper as a practical, selective, and reusable nanocatalyst in C–C and C–O coupling reactions

RSC Advances ◽  
2021 ◽  
Vol 11 (42) ◽  
pp. 25867-25879
Author(s):  
Parisa Moradi ◽  
Maryam Hajjami
Keyword(s):  
Graphene Oxide ◽  
Catalytic Activity ◽  
Magnetic Nanoparticles ◽  
Coupling Reactions ◽  
Graphene Oxide Nanosheets ◽  
Magnetic Graphene Oxide ◽  
Diaryl Ethers ◽  
Magnetic Graphene

Catalytic activity of supported copper on magnetic graphene oxide was investigated as a selective and reusable nanocatalyst in the synthesis of diaryl ethers and biphenyls.

Lewis Acid-Promoted Suzuki Reaction using Palladium Chloride Anchored on a Polymer as a Catalyst

2008 ◽  
Vol 61 (8) ◽  
pp. 610 ◽  
Author(s):  
Guozhi Fan ◽  
Hanjun Zhang ◽  
Siqing Cheng ◽  
Zhandong Ren ◽  
Zhijun Hu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Lewis Acid ◽  
Lewis Acids ◽  
Heterogeneous Catalysts ◽  
Suzuki Reaction ◽  
Cross Coupling ◽  
Palladium Chloride ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Recoverable Catalyst

Palladium chloride anchored on polystyrene modified by 5-amino-1,10-phenanthroline was prepared and used as an efficient recoverable catalyst for Suzuki cross-coupling reactions. The heterogeneous catalysts can be easily separated from the reaction mixture and reused for five cycles without significant Pd leaching and loss of catalytic activity. Rate enhancement in the Suzuki reaction by Lewis acids was also studied.

A graphdiyne-based carbon material for electroless deposition and stabilization of sub-nanometric Pd catalysts with extremely high catalytic activity

2019 ◽  
Vol 7 (21) ◽  
pp. 13142-13148 ◽  
Author(s):  
Liang-Liang Yang ◽  
Hong-Juan Wang ◽  
Juan Wang ◽  
Yu Li ◽  
Wen Zhang ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Carbon Material ◽  
Electroless Deposition ◽  
Suzuki Coupling ◽  
High Catalytic Activity ◽  
Coupling Reactions ◽  
Pd Catalysts ◽  
Catalytic Activities

A new graphdiyne-based carbon material was synthesized as an ideal substrate for electroless deposition and stabilization of sub-nanometric Pd catalysts, which showed extremely high catalytic activities for the reduction of nitroarenes and Suzuki coupling reactions.

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