ChemInform Abstract: NiCl2(PCy3)2: A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids.

ChemInform ◽  
2010 ◽  
Vol 33 (4) ◽  
pp. no-no
Author(s):  
Danilo Zim ◽  
Vanusa R. Lando ◽  
Jairton Dupont ◽  
Adriano L. Monteiro
Keyword(s):  
Cross Coupling ◽  
Catalyst Precursor ◽  
Efficient Catalyst ◽  
Arylboronic Acids ◽  
Aryl Tosylates

NiCl2(PCy3)2:  A Simple and Efficient Catalyst Precursor for the Suzuki Cross-Coupling of Aryl Tosylates and Arylboronic Acids

2001 ◽  
Vol 3 (19) ◽  
pp. 3049-3051 ◽  
Author(s):  
Danilo Zim ◽  
Vanusa R. Lando ◽  
Jairton Dupont ◽  
Adriano L. Monteiro
Keyword(s):  
Cross Coupling ◽  
Catalyst Precursor ◽  
Efficient Catalyst ◽  
Arylboronic Acids ◽  
Aryl Tosylates

Pd/Indanone-Based Ligands: An Efficient Catalyst System for Ullmann­-Type, Suzuki–Miyaura, and Mizoroki–Heck Cross-Coupling Reactions with Aryl Tosylates and Aryl Halides

Synthesis ◽  
2017 ◽  
Vol 49 (18) ◽  
pp. 4372-4382 ◽  
Author(s):  
Mohammed Waheed ◽  
Naseem Ahmed
Keyword(s):  
Catalytic Activity ◽  
Cross Coupling ◽  
Catalyst System ◽  
Aryl Halides ◽  
Maximum Efficiency ◽  
High Catalytic Activity ◽  
Coupling Reactions ◽  
Efficient Catalyst ◽  
Cross Coupling Reactions ◽  
Aryl Tosylates

2-Hydroxyindan-1-ones have been efficiently synthesized and successfully applied as ligands in Pd-catalyzed Ullmann type, Suzuki–Miyaura, and Mizoroki–Heck cross-coupling reactions with aryl tosylates and aryl halides. The ligands are air- and moisture-stable and have shown high catalytic activity with Pd(OAc)2 in these cross-coupling reactions. The system tolerates a variety of functional groups in the product and can be re-used at least three times with maximum efficiency.

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