Palladium-anchored multidentate SBA-15/di-urea nanoreactor: A highly active catalyst for Suzuki coupling reaction

2018 ◽  
Vol 32 (8) ◽  
pp. e4397 ◽  
Author(s):  
Sahar Rohani ◽  
Ghodsi Mohammadi Ziarani ◽  
Alireza Badiei ◽  
Abolfazl Ziarati ◽  
Maryam Jafari ◽  
...  

2014 ◽  
Vol 43 ◽  
pp. 75-78 ◽  
Author(s):  
Weijie Tang ◽  
Jing Li ◽  
Xiaodong Jin ◽  
Jian Sun ◽  
Jingwei Huang ◽  
...  


2011 ◽  
Vol 7 ◽  
pp. 310-319 ◽  
Author(s):  
Sanjay R Borhade ◽  
Suresh Babsaheb Waghmode

Palladium supported on nickel ferrite (Pd/NiF2O4) was found to be a highly active catalyst for the Suzuki coupling reaction between various aryl halides and arylboronic acids. The reaction gave excellent yields (70–98%) under ligand free conditions in a 1:1 DMF/H2O solvent mixture, in short reaction times (10–60 min). The catalyst could be recovered easily by applying an external magnetic field. The polyaryls were similarly synthesized.



2016 ◽  
Vol 6 (6) ◽  
pp. 1667-1676 ◽  
Author(s):  
Hui Liu ◽  
Tiesheng Li ◽  
Xiaoxia Xue ◽  
Wenjian Xu ◽  
Yangjie Wu

A SAM of Pd(FcL)–Si as a highly active and recyclable heterogeneous catalyst for Suzuki coupling reaction.



2019 ◽  
Vol 48 (10) ◽  
pp. 3214-3222 ◽  
Author(s):  
David Rendón-Nava ◽  
Alejandro Álvarez-Hernández ◽  
Arnold L. Rheingold ◽  
Oscar R. Suárez-Castillo ◽  
Daniel Mendoza-Espinosa

A series of hydroxyl functionalized PEPPSI complexes have been used as highly active catalyts for the Suzuki coupling of aryl chlorides/amides with boronic acids.



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