Recent Developments in Recyclable Copper Catalyst Systems for C–N Bond Forming Cross-Coupling Reactions Using Aryl Halides and Arylboronic Acids

2013 ◽  
pp. 119-171 ◽  
Author(s):  
Mannepalli Lakshmi Kantam ◽  
Chintareddy Venkat Reddy ◽  
Pottabathula Srinivas ◽  
Suresh Bhargava
Keyword(s):  
Copper Catalyst ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Bond Forming ◽  
Cross Coupling Reactions ◽  
Recent Developments ◽  
Catalyst Systems

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.

Recent Developments and Perspectives in the C-Se Cross Coupling Reactions

2020 ◽  
Vol 24 (11) ◽  
pp. 1230-1262 ◽  
Author(s):  
Diana Elizabeth Jose ◽  
U. S. Kanchana ◽  
Thomas V. Mathew ◽  
Gopinathan Anilkumar
Keyword(s):  
Cross Coupling ◽  
Environmentally Benign ◽  
Coupling Reactions ◽  
Organoselenium Compounds ◽  
Bond Forming ◽  
Design And Synthesis ◽  
Cross Coupling Reactions ◽  
Material Interest ◽  
Recent Developments ◽  
Low Toxicity

: The C-Se bond forming reactions are attractive synthetic strategies for biochemists and synthetic chemists alike for the synthesis of various molecules that are of biological, pharmaceutical and material interest. Therefore, the design and synthesis of organoselenium compounds currently constitute engaging fundamental problems in applied chemistry both in pharmaceutical and academic laboratories. This review discusses the recent works reported in carbon–selenium cross-coupling reactions with the emphasis on the mechanistic aspects of the reactions. The reacting species, the addition of ligands, selection of catalysts, use of suitable solvents, proper setting of reaction time, are well discussed to understand the detailed mechanism. Various simple, economical and environmentally friendly protocols are demonstrated, which ensured product stability, low toxicity, environmentally benign and excellent reactivity for the synthesis of organoselenium compounds. This review covers the scientific literature from 2010 to 2019.

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.

Nickel-catalysed Suzuki–Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids

2015 ◽  
Vol 58 ◽  
pp. 154-157 ◽  
Author(s):  
Man Wang ◽  
Xiaobin Yuan ◽  
Hongyu Li ◽  
Limin Ren ◽  
Zhizhong Sun ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Cross Coupling Reactions
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