the catalytic acvtivity of dimeric and monomeric ortho-palladated complexes [pd{c6h2(ch2nh2-(ome)2,3,4}(µ-cl)]2)2) and [pd{c6h2(ch2nh2-(ome)2,3,4}cl(pph3)](3), was investigated in heck cross-coupling reaction. these complexes are more active and efficient catalysts for heck cross-coupling reaction. the palladium complexes 2 and 3 is employed in the heck cross-coupling reaction between styrene a...

The catalytic acvtivity of dimeric and monomeric ortho-palladated complexes [Pd{C6H2(CH2NH2-(OMe)2,3,4}(µ-Cl)]2)2) and [Pd{C6H2(CH2NH2-(OMe)2,3,4}Cl(PPh3)](3), was investigated in Heck cross-coupling reaction. These complexes are more active and efficient catalysts for Heck cross-coupling reaction. The palladium complexes 2 and 3 is employed in the Heck cross-coupling reaction between styrene a...

Boronic pinacol ester group is not reactive in Kumada, Heck and Stille coupling reaction conditions. Fluorene-based sophisticated organoboron compounds were synthesized by means of Palladium catalyzed Kumada, Heck and Stille cross-coupling reactions from halofluorenyl boronic esters.

Since metal nanoparticles have a high surface-to-volume ratio and very active surface atoms, they are very attractive catalysts for a wide variety of organic and inorganic reactions, compared to bulk catalysts. Metal nanoparticles suspended in colloidal solutions and those adsorbed onto bulk supports have been used as catalysts for a wide variety of carbon-carbon bond formation reactions such a...

An efficient and stereoselective catalytic system for the Heck cross coupling reaction using novel 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (1, LHX) and Pd(OAc)2 loading has been reported. The palladium complexes derived from the salts 1a-f prepared in situ exhibit good catalytic activity in the Heck coupling reaction of aryl bromides under mild conditions.

A novel and efficient palladium-based homogeneous catalyst was fabricated and used as a robust catalyst in Suzuki–Miyaura cross-coupling and Heck reactions. 2-Amino-N(pyridin-2-ylmethyl)benzamide was introduced as a versatile ligand for palladiumcatalyzed cross-coupling reactions. The desired active and stable homogeneous Pd catalyst was prepared via the coordination of Pd with 2-amino-N-(pyrid...

this study offers an exclusive class of magnetic nanoparticles supported hyperbranched polyglycerol (mnp/hpg) that was functionalized with citric acid (mnp/hpg-ca) as a host immobilization of palladium nanoparticles. the mnp/hpg-ca/pd catalyst was fully characterized using some different techniques such as thermogravimetric analysis (tga), x-ray diffraction (xrd), transmission electron microsco...

Acyclic diaminocarbenes are found to be useful ligands for palladium catalyzed Suzuki-Miyaura, Sonogashira and Heck cross-coupling reactions of aryl/alkenyl bromides and chlorides.

Fe-MIL-101-isatin-Schiff-base-Co was synthesized and applied as a catalyst for Ullmann-type, Buchwald–Hartwig, Hirao, Hiyama Mizoroki–Heck cross-coupling reactions of aryl halides.

The Mizoroki-Heck as a cross-coupling method is one of the important reactions for Carbon-Carbon bond formation. This reaction permits substitution on planar sp2-hybridized carbon atom.