A general procedure for the fast Suzuki coupling of major families of heteroaryl bromides was realized by using Pd(OAc)2/PtBu3 as the catalyst. Many couplings were finished within minutes at room temperature in n-butanol. Different from previous studies, three typical heteroaryl bromides were systematically examined in couplings of various heteroaryl and aryl boronic acids
A highly effective method for palladium-catalyzed Suzuki-Miyaura coupling of aryl bromides and arylb...
Suzuki–Miyaura cross-coupling reactions of heteroaromatics catalyzed by palladium supported in the c...
The application of hexa[(dimethylamino)methyl]-functionalized triphenylphosphine (1) and its benzyla...
A Pd(OAc)2/(o-MeOPh)3P system has been developed for the catalytic Suzuki coupling of aryl bromides ...
Suzuki–Miyaura coupling of heteroaryls is an important method for the preparation of compound librar...
A robust palladium catalyst system supported by the hybrid ligand N-heterocyclic carbene along with ...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
The benzamide-derived P,O-ligands efficiently promoted the Pd-catalyzed Suzuki cross-coupling reacti...
Chapter 1. Highly active and efficient catalyst systems derived from palladium precatalysts and mono...
(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of a...
Transition metal-catalyzed cross-coupling reaction has become a useful methodology for the formation...
A Ruphos-mediated Suzuki cross-coupling between (hetero)aryl bromides and secondary alkyltrifluorobo...
Transition metal-catalyzed cross-coupling reaction has become a useful methodology for the formation...
The results of a ligand-free Pd(OAc)(2)-catalyzed Suzuki-Miyaura C-C coupling performed at room temp...
A Ruphos-mediated Suzuki cross-coupling between (hetero)aryl bromides and secondary alkyltrifluorobo...
A highly effective method for palladium-catalyzed Suzuki-Miyaura coupling of aryl bromides and arylb...
Suzuki–Miyaura cross-coupling reactions of heteroaromatics catalyzed by palladium supported in the c...
The application of hexa[(dimethylamino)methyl]-functionalized triphenylphosphine (1) and its benzyla...
A Pd(OAc)2/(o-MeOPh)3P system has been developed for the catalytic Suzuki coupling of aryl bromides ...
Suzuki–Miyaura coupling of heteroaryls is an important method for the preparation of compound librar...
A robust palladium catalyst system supported by the hybrid ligand N-heterocyclic carbene along with ...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
The benzamide-derived P,O-ligands efficiently promoted the Pd-catalyzed Suzuki cross-coupling reacti...
Chapter 1. Highly active and efficient catalyst systems derived from palladium precatalysts and mono...
(Figure presented) The first general examples of palladium-catalyzed Suzuki-type cross-coupling of a...
Transition metal-catalyzed cross-coupling reaction has become a useful methodology for the formation...
A Ruphos-mediated Suzuki cross-coupling between (hetero)aryl bromides and secondary alkyltrifluorobo...
Transition metal-catalyzed cross-coupling reaction has become a useful methodology for the formation...
The results of a ligand-free Pd(OAc)(2)-catalyzed Suzuki-Miyaura C-C coupling performed at room temp...
A Ruphos-mediated Suzuki cross-coupling between (hetero)aryl bromides and secondary alkyltrifluorobo...
A highly effective method for palladium-catalyzed Suzuki-Miyaura coupling of aryl bromides and arylb...
Suzuki–Miyaura cross-coupling reactions of heteroaromatics catalyzed by palladium supported in the c...
The application of hexa[(dimethylamino)methyl]-functionalized triphenylphosphine (1) and its benzyla...