scholarly journals Recent progress in application of nanocatalysts for carbonylative Suzuki cross-coupling reactions

RSC Advances ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 2112-2125
Author(s):  
Inci Söğütlü ◽  
Evan Abdulkarim Mahmood ◽  
Saeid Ahmadizadeh Shendy ◽  
Saeideh Ebrahimiasl ◽  
Esmail Vessally
Keyword(s):  
Carbon Monoxide ◽  
Recent Progress ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Cross Coupling Reactions ◽  
Carbon Carbon Bonds ◽  
Carbon Bonds

Cross-coupling of aryl halides and arylboronic acids in the presence of carbon monoxide, also called carbonylative Suzuki coupling, to form two new carbon–carbon bonds in the production of synthetically and biologically important biaryl ketones, has been widely studied.

scholarly journals Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions

RSC Advances ◽  
2021 ◽  
Vol 11 (43) ◽  
pp. 26883-26891
Author(s):  
Jairus L. Lamola ◽  
Paseka T. Moshapo ◽  
Cedric W. Holzapfel ◽  
Munaka Christopher Maumela
Keyword(s):  
Palladium Catalyst ◽  
Cross Coupling ◽  
Phosphine Ligands ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Cross Coupling Reactions ◽  
Catalyst Systems

Efficient palladium catalyst systems consisting of bench-stable biaryl phosphacycles and Pd(OAc)2 are described for Suzuki–Miyaura cross-coupling reactions of a diverse array of aryl halides and arylboronic acids.

Transition-metal-free, ambient-pressure carbonylative cross-coupling reactions of aryl halides with potassium aryltrifluoroborates

2015 ◽  
Vol 51 (44) ◽  
pp. 9133-9136 ◽  
Author(s):  
Fengli Jin ◽  
Wei Han
Keyword(s):  
Transition Metal ◽  
Ambient Pressure ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Metal Free ◽  
General Methodology ◽  
Cross Coupling Reactions

A transition-metal-free, ambient-pressure, and general methodology for carbonylative Suzuki coupling has been developed.

Application of organoselenides in the Suzuki, Negishi, Sonogashira and Kumada cross-coupling reactions

2015 ◽  
Vol 51 (85) ◽  
pp. 15522-15525 ◽  
Author(s):  
A. L. Stein ◽  
F. N. Bilheri ◽  
G. Zeni
Keyword(s):  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Carbon Carbon Bonds ◽  
Carbon Bonds ◽  
Palladium Catalyzed

A powerful tool for constructing new carbon–carbon bonds via palladium-catalyzed cross-coupling reactions of unsaturated organoselenides is described.

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