1043419-87-9

Upstream product

• 108717-96-0 1-benzyl-4-phenyl-1H-[1,2,3]triazole 
• 7335-27-5 ethyl 4-chlorobenzoate 
• 5798-75-4 Ethyl 4-bromobenzoate 
• 100-39-0 benzyl bromide 
• 536-74-3 phenylacetylene 

Relevant academic research and scientific papers

Copper(I) and palladium nanoparticles supported on ethylenediamine- functionalized cellulose as an efficient catalyst for the 1,3-dipolar cycloaddition/direct arylation sequence

Cu(I) and nanoparticles of Pd supported on ethylenediamine-functionalized cellulose as a novel bio-supported catalyst was synthesized and characterized. The synthesized catalyst was found to be a highly efficient heterogeneous catalyst for the synthesis o

C-H arylations of 1,2,3-triazoles by reusable heterogeneous palladium catalysts in biomass-derived γ-valerolactone

C-H arylations were accomplished with a user-friendly heterogeneous palladium catalyst in the biomass-derived γ-valerolactone (GVL) as an environmentally-benign reaction medium. The user-friendly protocol was characterized by ample substrate scope and hig

Catalytic direct arylations in polyethylene glycol (PEG): Recyclable palladium(O) catalyst for C-H bond cleavages in the presence of air

Two protocols for ruthenium- or palladium-catalyzed direct arylations In user-friendly polyethylene glycol (PEG) were devised, which set the stage for the development of user-friendly paliadium(0)-cataiyzed C-H bond functionalizations In the presence of a

Palladium-catalyzed direct arylations of 1,2,3-triazoles with aryl chlorides using conventional heating

Generally applicable, palladium-catalyzed direct arylations of 1,2,3-triazoles with aryl chlorides were accomplished through conventional heating at reaction temperatures of 105-120°C. Thereby, intra- and intermolecular C-H bond functionalizations were achieved with a variety of differently substituted chlorides as electrophiles, bearing numerous valuable functional groups.