0000000000522977

AUTHOR

Taoufik Boubaker

showing 3 related works from this author

Ambident electrophilicity of 4‐nitrobenzochalcogenadiazoles: Kinetic studies and structure‐reactivity relationships

2020

Inorganic ChemistryComputational chemistryChemistryOrganic ChemistryKineticsElectrophilePhysical and Theoretical ChemistryStructure reactivityKinetic energyBiochemistryInternational Journal of Chemical Kinetics
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Coordination Chemistry of a Bis(Tetrazine) Tweezer: A Case of Host-Guest Behavior with Silver Salts

2021

The carbon-carbon cross-coupling of phenyl s-tetrazine (Tz) units at their ortho-phenyl positions allows the formation of constrained bis(tetrazines) with original tweezer structures. In these compounds, the face-to-face positioning of the central tetrazine cores is reinforced by π-stacking of the electron-poor nitrogen-containing heteroaromatic moieties. The resulting tetra-aromatic structure can be used as a weak coordinating ligand with cationic silver. This coordination generates a set of bis(tetrazine)-silver(I) coordination complexes tolerating a large variety of counter anions of various geometries, namely, PF6−, BF4−, SbF6−, ClO4−, NTf2−, and OTf−. These compounds were characterized…

analytical_chemistrycoordinationAbsorption spectroscopyPharmaceutical ScienceCrystal structure010402 general chemistryElectrochemistryligand01 natural sciencesArticleXRD structureAnalytical ChemistryCoordination complexTetrazinechemistry.chemical_compoundQD241-441bis(tetrazine)Drug Discovery[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistrysilverPhysical and Theoretical Chemistryhost-guestchemistry.chemical_classification010405 organic chemistryLigandOrganic ChemistryCationic polymerization0104 chemical sciencesCrystallographychemistryChemistry (miscellaneous)Molecular MedicineStoichiometryMolecules
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Solvent-free ruthenium-catalysed triflate coupling as a convenient method for selective azole-o-C-H monoarylation.

2019

Metal-catalysed ortho-directed C–H functionalization usually faces selectivity issues in the competition between mono- and disubstitution processes. We report herein the ruthenium-catalysed N-directed C–H monoarylation of arylpyrazoles with a selectivity of up to 96% or that generally reaches values above 80%. This selectivity is an effect of solvent-free conditions associated with sulfonate reagents, in the absence of frequently used acidic additives.

chemistry.chemical_classificationSolvent free010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesRutheniumchemistry.chemical_compoundSulfonateReagentSurface modificationAzolePhysical and Theoretical ChemistrySelectivityTrifluoromethanesulfonateOrganicbiomolecular chemistry
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