ChemInform Abstract: Copper-Catalyzed Carbonylative Suzuki Coupling of Aryl Iodides with Arylboronic Acids under Ambient Pressure of Carbon Monoxide.

ChemInform ◽  
2015 ◽  
Vol 46 (14) ◽  
pp. no-no
Author(s):  
Laijin Cheng ◽  
Yanzhen Zhong ◽  
Zhuchao Ni ◽  
Hongyan Du ◽  
Fengli Jin ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Ambient Pressure ◽  
Suzuki Coupling ◽  
Arylboronic Acids ◽  
Aryl Iodides

Copper-catalyzed carbonylative Suzuki coupling of aryl iodides with arylboronic acids under ambient pressure of carbon monoxide

RSC Advances ◽  
2014 ◽  
Vol 4 (83) ◽  
pp. 44312-44316 ◽  
Author(s):  
Laijin Cheng ◽  
Yanzhen Zhong ◽  
Zhuchao Ni ◽  
Hongyan Du ◽  
Fengli Jin ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Ethylene Glycol ◽  
Ambient Pressure ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Poly Ethylene Glycol ◽  
Arylboronic Acids ◽  
Aryl Iodides ◽  
Poly Ethylene

An efficient and ligandless nanocopper-catalyzed carbonylative cross-coupling of aryl iodides with arylboronic acids at ambient CO pressure in poly(ethylene glycol), has been developed.

Transition metal-free, iodide-mediated domino carbonylation–benzylation of benzyl chlorides with arylboronic acids under ambient pressure of carbon monoxide

2016 ◽  
Vol 18 (9) ◽  
pp. 2598-2603 ◽  
Author(s):  
Fengli Jin ◽  
Yanzhen Zhong ◽  
Xin Zhang ◽  
Huichun Zhang ◽  
Qian Zhao ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Transition Metal ◽  
Ambient Pressure ◽  
Metal Free ◽  
Arylboronic Acids ◽  
Benzyl Chlorides

Transition metal-free, ambient-pressure domino carbonylation–benzylation reactions by iodide catalysis have been developed.

scholarly journals Carbonylative Suzuki coupling reactions of aryl iodides with arylboronic acids over Pd/SiC

2015 ◽  
Vol 36 (3) ◽  
pp. 322-327 ◽  
Author(s):  
Yanli Cui ◽  
Xiaoning Guo ◽  
Yingyong Wang ◽  
Xiangyun Guo
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Aryl Iodides

Transition-metal-free carbonylation of aryl halides with arylboronic acids by utilizing stoichiometric CHCl3 as the carbon monoxide-precursor

2019 ◽  
Vol 21 (11) ◽  
pp. 2911-2915 ◽  
Author(s):  
Fangning Xu ◽  
Dan Li ◽  
Wei Han
Keyword(s):  
Carbon Monoxide ◽  
Transition Metal ◽  
Suzuki Coupling ◽  
Free Carbon ◽  
Aryl Halides ◽  
Metal Free ◽  
Arylboronic Acids ◽  
General Methodology

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

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.

Resin-to-Resin Suzuki Coupling of Solid Supported Arylboronic Acids

2000 ◽  
Vol 2 (3) ◽  
pp. 228-231 ◽  
Author(s):  
Michel Gravel ◽  
Christian D. Bérubé ◽  
Dennis G. Hall
Keyword(s):  
Suzuki Coupling ◽  
Arylboronic Acids
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