Search results for "C−C coupling"

showing 7 items of 7 documents

SBA-15/POSS-Imidazolium Hybrid as Catalytic Nanoreactor

2019

Supported imidazolium modified polyhedral oligomeric silsesquioxanes (POSS) on SBA-15 have been used as platform for Pd(II) species. The so-obtained material was firstly characterized by means of TGA, solid state NMR, TEM, XPS, SAXS, porosimetry and ICP-OES and it was successfully tested as pre-catalyst in C−C cross couplings, namely Suzuki-Miyaura and Heck reactions. In both cases, the solid proved to be highly efficient and easily recoverable from the reaction mixture. The recyclability was verified for up to seven cycles without showing any activity decrease. Interestingly, only Pd(II) was detected in the reused catalyst in the Heck reaction. Therefore, the versatility of the material w…

ChemistryC−C couplingchemistry.chemical_elementGeneral ChemistryNanoreactorSettore CHIM/06 - Chimica OrganicaHeterogeneous catalysispalladiumCoupling reactionCatalysisC c couplingHeck reactionheterogeneous catalysisHeck reactionPolymer chemistryheterogeneous catalysiSuzuki-Miyaura reactionPalladiumAdvanced Synthesis and Catalysis
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Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups

2019

Abstract We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.

Denticityoxidation010405 organic chemistryChemistrySupporting electrolyteCommunicationC−C couplingoxygen heterocyclesSubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesEnvironmentally friendlyCombinatorial chemistryCommunicationsCatalysisCoupling reaction0104 chemical scienceschemistry.chemical_compoundElectrochemistry | Hot Paperelectrochemistrycross-couplingPolar effectPhenolsAngewandte Chemie International Edition
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A Next‐Generation Air‐Stable Palladium(I) Dimer Enables Olefin Migration and Selective C−C Coupling in Air

2020

Abstract We report a new air‐stable PdI dimer, [Pd(μ‐I)(PCy2 tBu)]2, which triggers E‐selective olefin migration to enamides and styrene derivatives in the presence of multiple functional groups and with complete tolerance of air. The same dimer also triggers extremely rapid C−C coupling (alkylation and arylation) at room temperature in a modular and triply selective fashion of aromatic C−Br, C−OTf/OFs, and C−Cl bonds in poly(pseudo)halogenated arenes, displaying superior activity over previous PdI dimer generations for substrates that bear substituents ortho to C−OTf.

Dimerchemistry.chemical_elementHomogeneous catalysisAlkylationmigration010402 general chemistry01 natural sciencesolefinCatalysisStyreneCatalysischemistry.chemical_compoundkatalyytitPolymer chemistryChemoselectivityOlefin fiber010405 organic chemistryCommunicationC−C couplingGeneral MedicineGeneral Chemistrypalladiumhomogeneous catalysisCommunications3. Good health0104 chemical scienceschemistrychemoselectivitykatalyysiddc:540Homogeneous Catalysis | Hot Paperolefin migrationPalladiumAngewandte Chemie International Edition
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Developments in the dehydrogenative electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol

2021

Abstract The symmetric biphenol 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol is a well‐known ligand building block and is used in transition‐metal catalysis. In the literature, there are several synthetic routes for the preparation of this exceptional molecule. Herein, the focus is on the sustainable electrochemical synthesis of 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol. A brief overview of the developmental history of this inconspicuous molecule, which is of great interest for technical applications, but has many challenges for its synthesis, is provided. The electro‐organic method is a powerful, sustainable, and efficient alternative to conventional synthesis to obtain this symmetric biphenol up to the …

Green chemistry540 Chemistry and allied sciencespolycycles010405 organic chemistryChemistryoxidationOrganic ChemistryC−C couplingMinireviewsGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesC c couplingelectrochemistry540 Chemiesustainable chemistryMinireviewC−C Coupling | Reviews Showcase
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Concise and modular synthesis of regioisomeric haptens for the production of high-affinity and stereoselective antibodies to the strobilurin azoxystr…

2011

The immune response to regioisomeric haptens of azoxystrobin with varied derivatization sites was studied. Based on the Sonogashira and Suzuki-Miyaura couplings and following a straightforward modular design, we have synthesized four haptens with the same linker anchored through C-C bonds and located at different sites of the molecule. The most stereoselective antibodies were produced from immunogens with the spacer arm at a distal position from the β-methoxyacrylate moiety characteristic of strobilurins. Moreover, we observed that assay cross-reactivity was reliant on the functionalization site of the competitor derivative. Finally, the antibody binding site was explored using synthetic ch…

Hapten designStereochemistryChemistryImmunochemistryOrganic ChemistryC−C couplingSonogashira couplingLandsteinerBiochemistryChemical synthesisStrobilurinschemistry.chemical_compoundMolecular recognitionLinker attachment siteDrug DiscoveryMoietyMolecular recognitionDerivatizationLinkerHaptenTetrahedron
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Catechol-Functionalized Carbon Nanotubes as Support for Pd Nanoparticles

2022

Carbon nanotubes have been covalently functionalized with catechol moieties through the formation of the corresponding aryl radicals obtained by reacting 4-aminocatechol with isoamyl nitrite. The functionalized multiwalled carbon nanotubes have been in turn used to immobilize Pd(II) ions on its surface forming catechol-Pd complexes, which were reduced to Pd nanoparticles (NPs). The so-obtained hybrid material has been characterized by means of thermogravimetric analysis coupled with differential scanning calorimetry (TGA-DSC), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). This latter technique allowed to estimate the nanoparticle size (5.7 +/- 2.8 nm) wh…

Heterogeneous catalysisSuzuki and Heck reactionsOrganic ChemistryC-C coupling reactionsC−C coupling reactionsCarbon nanotubesPhysical and Theoretical ChemistryPalladium nanoparticlesEuropean Journal of Organic Chemistry
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Carbocatalytic Oxidative Dehydrogenative Couplings of (Hetero)Aryls by Oxidized Multi‐Walled Carbon Nanotubes in Liquid Phase

2019

HNO3-oxidized carbon nanotubes catalyze oxidative dehydrogenative (ODH) carbon-carbon bond formation between electron-rich (hetero)aryls with O-2 as a terminal oxidant. The recyclable carbocatalytic method provides a convenient and an operationally easy synthetic protocol for accessing various benzofused homodimers, biaryls, triphenylenes, and related benzofused heteroaryls that are highly useful frameworks for material chemistry applications. Carbonyls/quinones are the catalytically active site of the carbocatalyst as indicated by model compounds and titration experiments. Further investigations of the reaction mechanism with a combination of experimental and DFT methods support the compet…

Reaction mechanism116 Chemical sciencesoxidative dehydrogenative couplingLiquid phaseOxidative phosphorylationCarbon nanotube010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysislaw.inventionlawcarbon nanotubecarbon nanotubesbiology010405 organic chemistryChemistryOrganic ChemistryC−C couplingCationic polymerizationcarbon nanotubes; C−C coupling; heterogeneous catalysis; oxidative dehydrogenative couplingActive siteGeneral ChemistryCombinatorial chemistry0104 chemical sciencesheterogeneous catalysisbiology.proteinheterogeneous catalysiTitrationC-C couplingChemistry – A European Journal
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