Search results for "C c coupling"

showing 3 items of 23 documents

ChemInform Abstract: Light Induced C-C Coupling of 2-Chlorobenzazoles with Carbamates, Alcohols, and Ethers.

2016

A light induced, transition-metal-free C-C coupling reaction of 2-chlorobenzazoles with aliphatic carbamates, alcohols, and ethers is presented. Inexpensive reagents, namely sodium acetate, benzophenone, water, and acetonitrile, are employed in a simple reaction protocol using a cheap and widely available 25 W energy saving UV-A lamp at ambient temperature.

chemistry.chemical_compoundC c couplingchemistryReagentLight inducedBenzophenoneOrganic chemistryGeneral MedicineAcetonitrileSodium acetateCoupling reactionChemInform
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Templating effect of carbon nanoforms on highly cross-linked imidazolium network: Catalytic activity of the resulting hybrids with Pd nanoparticles

2019

Two different carbon nanoforms (CNFs), namely multi-walled carbon nanotubes (MWCNTs) and carbon nanohorns (CNHs), have been chosen as support for the direct polymerization of a bis-vinylimidazolium salt. Transmission electron microscopy analyses revealed a templating effect of the CNFs on the growth of the polymeric network, which perfectly covers their whole surfaces creating a cylindrical or spherical coating for MWCNTs and CNHs, respectively. Subsequently, the CNFs-polyimidazolium have been used as stabilizers for Pd nanoparticles (Pd NPs), and the obtained materials have been characterized by means of analytical and spectroscopic techniques and then employed as easily recoverable and re…

chemistry.chemical_elementSettore CHIM/06 - Chimica OrganicaGeneral ChemistryHeterogeneous catalysisCatalysisnanotubesInorganic ChemistrySuzuki–Miyaura reactionC c couplingHeck reactionheterogeneous catalysischemistryHeck reactionPd nanoparticlesPolymer chemistrynanotubeheterogeneous catalysiC-C couplingSuzuki-Miyaura reactionCarbon
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Cross-Linked Thiazolidine Network as Support for Palladium: A New Catalyst for Suzuki and Heck Reactions

2015

A thiazolidine-based material was used for the first time as support for palladium. The support was prepared by starting from a highly cross-linked thiazolium-based material, obtained by radical oligomerization of a bisvinylthiazolium dibromide salt in the presence of 3-mercaptopropyl-modified silica SBA-15. Palladium was immobilized by treatment with tetrachloropalladate salt. Reduction with sodium borohydride afforded a thiazolidine-based material that acted as ligands for the Pd species. The thiazolidine-based palladium catalyst was fully characterized and, working in only 0.1 mol% amount, displayed good activity in the Suzuki-Miyaura and in the Heck reactions. Several biphenyl and alken…

metal catalysisThiazolidinechemistry.chemical_elementHeterogeneous catalysisCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundC c couplingN ligandsHeck reactioncross-couplingOrganic chemistryPhysical and Theoretical ChemistryS ligandsgreen chemistryOrganic ChemistrySettore CHIM/06 - Chimica Organicapalladiumheterogeneous catalysischemistryheterogeneous catalysis cross-coupling metal catalysis green chemistryheterogeneous catalysiC-C couplingPalladiumN ligand
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