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Radical Based Arylation Methods
(Wiley, 2009)
Most of the radical reactions can be conducted under mild conditions. In contrast to ionic reactions and many transition-metal mediated processes most of the functional groups are tolerated under radical conditions. Moreover, ...
Palladium catalysed regioselective arylation of indoles, benzofuran and benzothiophene with aryldiazonium salts
(Royal Soc ChemistryCambridgeInglaterra, 2012)
Radical Arylations
(John Wiley & Sons Ltd, 2012)
This chapter reports on radical arylations also highlighting the very important early achievements on this chemistry. To be named at this place are the Meerwein arylation and the Pschorr reaction. Intramolecular homolytic ...
N-Heterocyclic carbene copper(I) complex-catalyzed synthesis of 2-aryl benzoxazoles and benzothiazoles
(2016)
A new and efficient synthesis of 2-arylbenzoxazoles and benzothiazoles using a copper N-heterocyclic carbene complex is described. In a simple protocol a variety of 2-substituted benzoxazoles and benzothiazoles were obtained ...
Copper nanoparticles supported on zinc oxide as efficient catalyst for the N-Arylation of (Hetero)cyclic and acyclic amides
(WILEY-V C H VERLAG GMBH, 2021)
Copper nanoparticles (CuNPs) supported on ZnO are highly active and selective heterogeneous catalyst for the N-arylation of cyclic and acyclic amides (Golberg coupling). The reaction conditions are mild, featuring K3PO4 ...
Synthesis of triaryls: hydroxy and amine dinaphthyl anddiphenanthryl aryls by one-pot electron-transfer nucleophilicsubstitution reactions
(Pergamon-Elsevier Science Ltd., 2014-01)
A new one-pot synthetic route to achieve the preparation of hydroxy and amine binaphthyl and biphenanthryl aryls is here reported. This approach involves the reaction of 1,4-bromoiodobenzene, 4,4′-diiodobiphenyl, and 1,4- ...
Substitution Effects in Aryl Halides and Amides into the Reaction Mechanism of Ullmann-Type Coupling Reactions
(2024)
In this article, we present a comprehensive computational investigation into the reaction mechanism of N-arylation of substituted aryl halides through Ullmann-type coupling reactions. Our computational findings, obtained ...