Animal-bone-meal-supported palladium (0) was prepared and used as catalyst in the Suzuki coupling reaction in water, under sunlight as an alternative source of energy. This palladium has showed a high catalytic activity than tetrakis(triphenylphosphine) palladium (Pd(PPh3)4) in the Suzuki cross-coupling reaction (the reaction of 4-halogenopyridopyrimidine with boronic acids) in water via sunlight as the light source, with no addition of ligands. This green method affords heteroaryls with excellent yields in comparison with the classical method using tetrakis(triphenylphosphine) palladium. The green catalyst did not show any significant loss of activity, even when used up to five times
A simple and efficient protocol is described for a Suzuki reaction catalyzed by poly(vinyl chloride)...
The palladium-catalyzed Suzuki–Miyaura cross-coupling reaction of organic halides with boronic acids...
Suzuki–Miyaura cross-coupling remains a powerful tool in organic synthesis for C–C bond formation an...
<p>Animal-bone-meal-supported palladium (0) was prepared and used as catalyst in the Suzuki coupling...
Supported palladium catalyst 1 has been prepared by the immobilisation of [Pd(COD)Cl-2] (COD = 1,5-c...
A study on room temperature Suzuki cross-coupling in an aqueous medium was carried out using a simpl...
Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides (2a-d) have been prepared and characterized by co...
Among the various new challenges of chemical processes in water, research on stable, highly active, ...
WOS: 000398425800048PubMed: 28254611In catalytic systems, the support materials need to be both eco ...
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki ...
This review with 206 references covers the literature published until March 2004 on the development ...
WOS: 000251574200010Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides(2a-d) have been prepared and ...
We report a simple and efficient procedure for the ligand-free as well as ligand-assisted Suzuki rea...
A facile and less expensive monophosphinite ligand 2-(diphenylphosphinoxy)-naphthyl, C10H7OPPh2(1) h...
A highly efficient Suzuki cross-coupling reaction between phenyl bromide and phenylboronic acid cata...
A simple and efficient protocol is described for a Suzuki reaction catalyzed by poly(vinyl chloride)...
The palladium-catalyzed Suzuki–Miyaura cross-coupling reaction of organic halides with boronic acids...
Suzuki–Miyaura cross-coupling remains a powerful tool in organic synthesis for C–C bond formation an...
<p>Animal-bone-meal-supported palladium (0) was prepared and used as catalyst in the Suzuki coupling...
Supported palladium catalyst 1 has been prepared by the immobilisation of [Pd(COD)Cl-2] (COD = 1,5-c...
A study on room temperature Suzuki cross-coupling in an aqueous medium was carried out using a simpl...
Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides (2a-d) have been prepared and characterized by co...
Among the various new challenges of chemical processes in water, research on stable, highly active, ...
WOS: 000398425800048PubMed: 28254611In catalytic systems, the support materials need to be both eco ...
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki ...
This review with 206 references covers the literature published until March 2004 on the development ...
WOS: 000251574200010Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides(2a-d) have been prepared and ...
We report a simple and efficient procedure for the ligand-free as well as ligand-assisted Suzuki rea...
A facile and less expensive monophosphinite ligand 2-(diphenylphosphinoxy)-naphthyl, C10H7OPPh2(1) h...
A highly efficient Suzuki cross-coupling reaction between phenyl bromide and phenylboronic acid cata...
A simple and efficient protocol is described for a Suzuki reaction catalyzed by poly(vinyl chloride)...
The palladium-catalyzed Suzuki–Miyaura cross-coupling reaction of organic halides with boronic acids...
Suzuki–Miyaura cross-coupling remains a powerful tool in organic synthesis for C–C bond formation an...