Oxidative C−H/C−H Cross-Coupling Reactions between N -Acylanilines and Benzamides Enabled by a Cp*-Free RhCl3 /TFA Catalytic System

2018 ◽  
Vol 57 (29) ◽  
pp. 9108-9112 ◽  
Author(s):  
Yang Shi ◽  
Luoqiang Zhang ◽  
Jingbo Lan ◽  
Min Zhang ◽  
Fulin Zhou ◽  
...  
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

Novel cross-coupling reactions between organotellurides and Grignard reagents employing a MnCl2/CuI catalytic system

2012 ◽  
Vol 53 (28) ◽  
pp. 3556-3559 ◽  
Author(s):  
Marcio S. Silva ◽  
Renan S. Ferrarini ◽  
Bruno A. Sousa ◽  
Fabiano T. Toledo ◽  
João V. Comasseto ◽  
...  
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Grignard Reagents ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

Oxidative C−H/C−H Cross-Coupling Reactions between N -Acylanilines and Benzamides Enabled by a Cp*-Free RhCl3 /TFA Catalytic System

2018 ◽  
Vol 130 (29) ◽  
pp. 9246-9250 ◽  
Author(s):  
Yang Shi ◽  
Luoqiang Zhang ◽  
Jingbo Lan ◽  
Min Zhang ◽  
Fulin Zhou ◽  
...  
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

Pd(OAc)2/DABCO as an Inexpensive and Efficient Catalytic System for Hiyama­ Cross-Coupling Reactions of Aryl Halides with Aryltrimethoxysilanes

Synthesis ◽  
2005 ◽  
Vol 2005 (18) ◽  
pp. 3039-3044 ◽  
Author(s):  
Jin-Heng Li ◽  
Chen-Liang Deng ◽  
Wen-Jie Liu ◽  
Ye-Xiang Xie
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

Application of a 2-aryl indenylphosphine ligand in the Buchwald–Hartwig cross-coupling reactions of aryl and heteroaryl chlorides under the solvent-free and aqueous conditions

2017 ◽  
Vol 15 (27) ◽  
pp. 5805-5810 ◽  
Author(s):  
Yan Liu ◽  
Jia Yuan ◽  
Zi-Fei Wang ◽  
Si-Hao Zeng ◽  
Meng-Yue Gao ◽  
...  
Keyword(s):  
Catalytic System ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Solvent Free ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Cross Coupling Reaction ◽  
Aqueous Conditions

An efficient solvent-free and aqueous protocol for the Buchwald–Hartwig cross-coupling reaction has been developed. Notably, the catalytic system also efficiently catalyzed the reaction under aqueous conditions.

A simple catalytic system based on PdCl2(CH3CN)2 in water for cross-coupling reactions using diazonium salts

Tetrahedron ◽  
2013 ◽  
Vol 69 (46) ◽  
pp. 9761-9765 ◽  
Author(s):  
Ouissam El Bakouri ◽  
Martí Fernández ◽  
Sandra Brun ◽  
Anna Pla-Quintana ◽  
Anna Roglans
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Diazonium Salts ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

ChemInform Abstract: Pd(OAc)2in WERSA: A Novel Green Catalytic System for Suzuki-Miyaura Cross-Coupling Reactions at Room Temperature.

ChemInform ◽  
2015 ◽  
Vol 46 (47) ◽  
pp. no-no
Author(s):  
Preeti Rekha Boruah ◽  
Abdul Aziz Ali ◽  
Mitali Chetia ◽  
Bishwajit Saikia ◽  
Diganta Sarma
Keyword(s):  
Catalytic System ◽  
Room Temperature ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions

Studies of palladium-catalyzed coupling reactions for preparation of hindered 3-arylpyrroles relevant to (-)-rhazinilam and its analogues

2001 ◽  
Vol 79 (11) ◽  
pp. 1827-1839 ◽  
Author(s):  
Léon Ghosez ◽  
Cécile Franc ◽  
Frédéric Denonne ◽  
Claire Cuisinier ◽  
Roland Touillaux
Keyword(s):  
Catalytic System ◽  
Broad Spectrum ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Cross Coupling Reactions ◽  
Reverse Process ◽  
Palladium Catalyzed ◽  
Palladium Coupling

Suzuki cross-coupling reactions of 3-pyrroleboronic acid derivatives with haloaromatics and the reverse process i.e., the coupling of 3-iodo(bromo)pyrroles with arylboronic acids have been investigated as a potential key step in the synthesis of (–)-rhazinilam and analogues. It was found that 3-iodo-2-formyl-1-tosylpyrroles efficiently coupled with a variety of arylboronic acids in the presence of PdCl2(dppf) as catalyst. This catalytic system is compatible with a broad spectrum of arylboronic acids — electron-rich, electron-poor, hindered, heterocyclic — which easily coupled with the pyrrole substrate.Key words: 2-substituted-3-arylpyrroles, biaryls, coupling reactions, arylboronic acids, palladium coupling, catalysis.

ChemInform Abstract: A Highly Active Catalytic System for Suzuki-Miyaura Cross-Coupling Reactions of Aryl and Heteroaryl Chlorides in Water.

ChemInform ◽  
2013 ◽  
Vol 44 (19) ◽  
pp. no-no
Author(s):  
Shu-Lan Mao ◽  
Yue Sun ◽  
Guang-Ao Yu ◽  
Cui Zhao ◽  
Zhi-Jun Han ◽  
...  
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Highly Active

An active catalytic system for Suzuki–Miyaura cross-coupling reactions using low levels of palladium loading

2017 ◽  
Vol 15 (18) ◽  
pp. 3924-3929 ◽  
Author(s):  
Meng-Qi Yan ◽  
Jia Yuan ◽  
Fang Lan ◽  
Si-Hao Zeng ◽  
Meng-Yue Gao ◽  
...  
Keyword(s):  
Catalytic System ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Low Levels
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