Pd–Co3[Co(CN)6]2 hybrid nanoparticles: preparation, characterization, and challenge for the Suzuki–Miyaura coupling of aryl chlorides under mild conditions

2016 ◽  
Vol 45 (2) ◽  
pp. 539-544 ◽  
Author(s):  
Ren Li ◽  
Ran Li ◽  
Changlai Wang ◽  
Lei Gao ◽  
Qianwang Chen
Keyword(s):  
High Activity ◽  
Suzuki Coupling ◽  
Simple Approach ◽  
Hybrid Nanoparticles ◽  
Aryl Chlorides ◽  
Mild Conditions

A simple approach for the synthesis of a Pd–MOF nanocatalyst with high activity for Suzuki coupling of aryl chlorides was reported.

Efficient symmetrical bidentate dioxime ligand-accelerated homogeneous palladium-catalyzed Suzuki–Miyaura coupling reactions of aryl chlorides

2017 ◽  
Vol 41 (1) ◽  
pp. 372-376 ◽  
Author(s):  
Jinyi Song ◽  
Hongyan Zhao ◽  
Yang Liu ◽  
Huatao Han ◽  
Zhuofei Li ◽  
...  
Keyword(s):  
High Activity ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Bidentate Ligands ◽  
Aryl Chlorides ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
Cross Coupling Reactions ◽  
Palladium Catalyzed

A series of N,O-bidentate ligands were synthesized and studied as high activity ligands for palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl chlorides with arylboronic acids under mild conditions.

Extremely High Activity Catalysts for the Suzuki Coupling of Aryl Chlorides: The Importance of Catalyst Longevity.

ChemInform ◽  
2003 ◽  
Vol 34 (18) ◽  
Author(s):  
Robin B. Bedford ◽  
Samantha L. Hazelwood ◽  
Michael E. Limmert
Keyword(s):  
High Activity ◽  
Suzuki Coupling ◽  
Aryl Chlorides

Chiral Mn(III) Salen Complex Immobilized on CuFe2O4@SiO2-NH2 NPs: A Cheap and Efficient Catalyst for N-arylation of Aryl Halides and Phenylboronic Acid Under Mild Conditions

2020 ◽  
Vol 17 (11) ◽  
pp. 857-863
Author(s):  
Mohammad Ali Nasseri ◽  
Seyyedeh Ameneh Alavi ◽  
Milad Kazemnejadi ◽  
Ali Allahresani
Keyword(s):  
Phenylboronic Acid ◽  
Significant Loss ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Efficient Catalyst ◽  
Aryl Chlorides ◽  
Mild Conditions ◽  
Cross Coupling Reactions ◽  
Salen Complex ◽  
Ft Ir

A convenient and efficient chiral CuFe2O4@SiO2-Mn(III) Ch.salen nanocatalyst has been developed for the C-N cross-coupling reactions of aryl halides/ phenylboronic acid with N-heterocyclic compounds in water and/or DMSO under mild conditions. The catalyst could be applied for the N-arylation of a variety of nitrogen-containing heterocycles with aryl chlorides, bromides, iodides and phenylboronic acid under mild conditions. Moderate to good yields were achieved for all substrates. The structure of catalyst was characterized using various techniques including FT-IR, FE-SEM, EDX, XRD, TEM and TGA. The catalyst can be simply recovered and reused for several times without significant loss of activity.

scholarly journals Pd/Ni-Catalyzed Germa-Suzuki coupling via dual Ge–F bond activation

2021 ◽  
Author(s):  
Hajime Kameo ◽  
Akihiro Mushiake ◽  
Tomohito Isasa ◽  
Hiroyuki Matsuzaka ◽  
Didier Bourissou
Keyword(s):  
Bond Activation ◽  
Suzuki Coupling ◽  
Mild Conditions ◽  
Dual Activation

Pd/Ni → Ge–F interactions supported by phosphine-chelation were found to trigger dual activation of Ge–F bonds under mild conditions.

Di- and tri-alkylphosphine adducts of S-donor palladacycles as catalysts in the Suzuki coupling of aryl chlorides

2004 ◽  
pp. 3864 ◽  
Author(s):  
Robin B. Bedford ◽  
Catherine S. J. Cazin ◽  
Michael B. Hursthouse ◽  
Mark E. Light ◽  
V�ronique J. M. Scordia
Keyword(s):  
Suzuki Coupling ◽  
Aryl Chlorides

ChemInform Abstract: New Cyclopalladated Benzothiophenes: A Catalyst Precursor for the Suzuki Coupling of Deactivated Aryl Chlorides.

ChemInform ◽  
2010 ◽  
Vol 41 (49) ◽  
pp. no-no
Author(s):  
Madavu Salian Subhas ◽  
Shailesh S. Racharlawar ◽  
B. Sridhar ◽  
P. Kavin Kennady ◽  
Pravin R. Likhar ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Catalyst Precursor ◽  
Aryl Chlorides
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