The Suzuki cross-coupling reaction in pure water catalyzed by ligandless palladium using polyethylene glycol derivatives as surfactant

2013 ◽  
Vol 27 (10) ◽  
pp. 615-618 ◽  
Author(s):  
Liu Xiang ◽  
Zhao Xiaohua ◽  
Lu Ming
Synlett ◽  
2010 ◽  
Vol 2010 (11) ◽  
pp. 1657-1660 ◽  
Author(s):  
Xi-Cun Wang ◽  
Guo-Jun Yang ◽  
Zheng-Jun Quan ◽  
Peng-Yan Ji ◽  
Jun-Ling Liang ◽  
...  

2001 ◽  
Vol 3 (3) ◽  
pp. 146-148 ◽  
Author(s):  
Vasudevan V. Namboodiri ◽  
Rajender S. Varma

RSC Advances ◽  
2014 ◽  
Vol 4 (78) ◽  
pp. 41510-41520 ◽  
Author(s):  
Jianfei Sheng ◽  
Fei Mao ◽  
Jun Yan ◽  
Ling Huang ◽  
Xingshu Li

A series of new ortho-(3,4,5-trimethoxybenzoyl)-acetanilides were synthesised by the cross-coupling reaction catalyzed with Pd catalyst in aqueous medium, with polyethylene glycol as additive under very mild conditions.


2012 ◽  
Vol 550-553 ◽  
pp. 639-642
Author(s):  
Fawang Li ◽  
Quan Ling Suo ◽  
Hai Long Hong ◽  
Li Min Han

The environmentally benign Suzuki cross-coupling reaction was developed by using ScCO2(Supercritical CO2) instead of traditionally organic solvent. In the paper the compound phenylferrocene was synthesized by the Suzuki cross-coupling reaction of iodoferrocene and phenylboronic acids in ScCO2/PEG (polyethylene glycol) with excellent yield ratio in the presence of ligand-free Pd/C catalyst and K2CO3.1.5H2O as base. The Pd/C catalyst can be reused by simply washing sequence and CO2can be recycled after depressurization. The catalytic reaction conditions were optimized in the reaction using ScCO2as solvent.


Synlett ◽  
2021 ◽  
Author(s):  
Misa Kawase ◽  
Kyosuke Matsuoka ◽  
Tsutomu Shinagawa ◽  
Go Hamasaka ◽  
Yasuhiro Uozumi ◽  
...  

This paper describes the Suzuki-Miyaura cross coupling reaction of aryl bromides with potassium aryltrifluoroborates in water catalyzed by linear polystyrene-stabilized PdO nanoparticles (PS-PdONPs). The reaction of aryl bromides having electron withdrawing groups or electron donating groups took place smoothly to give the corresponding coupling product in high yields. The catalyst recycles five times without significant loss of catalytic activity although a little bit increase in size of Pd NPs was observed after the reaction.


RSC Advances ◽  
2018 ◽  
Vol 8 (43) ◽  
pp. 24231-24235 ◽  
Author(s):  
Jingbo Li ◽  
Ping Huo ◽  
Junwei Zheng ◽  
Xiuming Zhou ◽  
Wanyun Liu

The water-soluble fullerene-supported PdCl2 nanocatalyst [C60-TEGS/PdCl2] exhibits high activity and recycling in pure water toward the Suzuki–Miyaura cross-coupling reaction.


RSC Advances ◽  
2014 ◽  
Vol 4 (87) ◽  
pp. 46926-46929 ◽  
Author(s):  
Gwénaëlle Hervé ◽  
Christophe Len

For the first time, a palladium catalyzed Heck cross-coupling reaction between 5-iodo-2′-deoxyuridine and various acrylate derivatives was performed using ligand-free conditions and microwave assistance in pure water.


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