Search results for "Oxadiazole"

showing 10 items of 183 documents

CCDC 685583: Experimental Crystal Structure Determination

2009

Related Article: P.Gomez-Saiz, R.Gil-Garcia, M.A.Maestro, F.J.Arnaiz, L.Lezama, T.Rojo, J.L.Pizarro, M.I.Arriortua, M.Gonzalez-Alvarez, J.Borras, V.Diez-Gomez, J.Garcia-Tojal|2009|Eur.J.Inorg.Chem.||373|doi:10.1002/ejic.200800812

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-(bis(mu~2~-thiocyanato)-(2-amino-5-(pyridin-2-yl)-134-oxadiazole)-copper(ii))Experimental 3D Coordinates
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CCDC 685584: Experimental Crystal Structure Determination

2009

Related Article: P.Gomez-Saiz, R.Gil-Garcia, M.A.Maestro, F.J.Arnaiz, L.Lezama, T.Rojo, J.L.Pizarro, M.I.Arriortua, M.Gonzalez-Alvarez, J.Borras, V.Diez-Gomez, J.Garcia-Tojal|2009|Eur.J.Inorg.Chem.||373|doi:10.1002/ejic.200800812

Space GroupCrystallographyCrystal SystemCrystal Structurecatena-((mu~2~-dicyanamido)-(mu~2~-2-methylamino-5-(pyridin-2-yl)-134-oxadiazole)-copper(ii) perchlorate monohydrate)Cell ParametersExperimental 3D Coordinates
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CCDC 749593: Experimental Crystal Structure Determination

2011

Related Article: A.Terenzi, G.Barone, A.P.Piccionello, G.Giorgi, A.Guarcello, P.Portanova, G.Calvaruso, S.Buscemi, N.Vivona, A.Pace|2010|Dalton Trans.|39|9140|doi:10.1039/c0dt00266f

Space GroupCrystallographybis(35-bis(2-pyridyl)-124-oxadiazole)-diaqua-copper(ii) diperchlorateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 685581: Experimental Crystal Structure Determination

2009

Related Article: P.Gomez-Saiz, R.Gil-Garcia, M.A.Maestro, F.J.Arnaiz, L.Lezama, T.Rojo, J.L.Pizarro, M.I.Arriortua, M.Gonzalez-Alvarez, J.Borras, V.Diez-Gomez, J.Garcia-Tojal|2009|Eur.J.Inorg.Chem.||373|doi:10.1002/ejic.200800812

Space GroupCrystallographybis(mu~2~-malonato)-bis(2-methylamino-5-(pyridin-2-yl)-134-oxadiazole)-di-copper(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Host−Guest Interactions between β-Cyclodextrin and the (Z)-Phenylhydrazone of 3-Benzoyl-5-phenyl-1,2,4-oxadiazole:  The First Kinetic Study of a Ring…

2002

The effect of beta-cyclodextrin (beta-CD) on the mononuclear heterocyclic rearrangement of the (Z)-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1) in aqueous borate buffer at pH = 9.6 has been analyzed at temperatures ranging from 293.15 to 313.15 K. The trend of the absorption spectra of 1 as a function of time has been accounted for with the formation of two different 1:1 complexes between beta-CD and 1, the first, "unreactive" complex being formed faster than the "reactive" one. The occurrence of negative activation enthalpy values for the studied interconversion evidences the kinetic relevance of inclusion processes. Computational models elaborated using the MM2 molecular mec…

Spectrophotometry InfraredStereochemistryOxadiazoleHydrazoneBeta-CyclodextrinsStereoisomerismOxadiazoleRing (chemistry)Medicinal chemistryInclusion compoundchemistry.chemical_compoundCyclodextrin host-guest interactionsCyclodextrinMoleculeSolutionKineticchemistry.chemical_classificationCyclodextrinsOxadiazolesMolecular StructureCyclodextrinbeta-CyclodextrinsOrganic ChemistryHydrazonesWaterStereoisomerismSettore CHIM/06 - Chimica OrganicaHydrazoneSolutionsKineticsModels ChemicalchemistryCyclization
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Synthesis of platinum complexes with 2-(5-perfluoroalkyl-1,2,4-oxadiazol-3yl)-pyridine and 2-(3-perfluoroalkyl-1-methyl-1,2,4-triazole-5yl)-pyridine …

2016

Five new mononuclear Pt(II) complexes with 5-perfluoroalkyl-1,2,4-oxadiazolyl-pyridine and 3-perfluoroalkyl-1,2,4-triazolyl-pyridine ligands are reported. The ligands 2-(5-perfluoroheptyl-1,2,4-oxadiazole-3yl)-pyridine (pfhop), 2-(5-perfluoropropyl)-1,2,4-oxadiazole-3yl)-pyridine (pfpop), 2-(3-perfluoroheptyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfhtp), 2-(3-perfluoropropyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfptp) and their complexes [PtCl2(pfhop)(2)]center dot 1.5 DMSO (2a), [PtCl2(pfpop)(2)]center dot 1.5 DMSO (3a), [PtCl2(pfhtp)(2)]center dot 1.5 DMSO (4a), PtCl2(pfhtp) (4b), [PtCl2(PfPtP)(2)]center dot 1.5 DMSO (5a) have been synthesized and structurally characterized. The comple…

Spectrophotometry InfraredStereochemistryPyridinesProton Magnetic Resonance SpectroscopyTriazoleOxadiazoleAntineoplastic AgentsApoptosisPlatinum Compounds010402 general chemistryLigands01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundSettore BIO/10 - BiochimicaCell Line TumorEthidiumPyridineMoleculeHumansFluorescent DyesPlatinum complexes oxadiazole antitumor activity010405 organic chemistryLigandAcridine orange124-TriazoleSettore CHIM/06 - Chimica OrganicaAcridine Orange0104 chemical scienceschemistrySettore CHIM/03 - Chimica Generale E InorganicaEthidium bromideJournal of inorganic biochemistry
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A new palladium(II)-catalyzed [3,3] aza-Claisen rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles

2011

Abstract A new efficient palladium(II)-catalyzed [3,3] aza-Claisen, formal sigmatropic rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles was developed. The mechanism was studied by analyzing the regiochemical and stereochemical course of the reaction. The results obtained indicated the intervention of a cationic pallada-cycle similar to the one postulated for the Cope rearrangement of 1,5-dienes.

StereochemistryArylOrganic ChemistryCationic polymerizationchemistry.chemical_elementSettore CHIM/06 - Chimica OrganicaSigmatropic reactionBiochemistryCarroll rearrangementAza-Claisen 124-Oxadiazoles 124-Oxadiazolones PalladiumCatalysisClaisen rearrangementchemistry.chemical_compoundchemistryDrug DiscoveryPalladiumCope rearrangement
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Isomerization and rearrangement of (E)- and (Z)-phenylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole: evidence for a “new” type of acid-catalysis …

2008

A kinetic investigation in methanol of the title reaction has evidenced the occurrence of two processes: the 1-E1-Z isomerization and the rearrangement of the (Z)-isomer into the relevant 4-benzoylamino-2,5-diphenyl-1,2,3-triazole (1-Z  T). The latter reaction is in line with the ability of the (Z)-phenylhydrazones of 3-benzoyl-1,2,4-oxadiazoles to undergo the so called mononuclear rearrangement of heterocycles (MRH). The occurrence of both the examined reactions is dependent on a Lewis-acid-catalysis. The obtained results have shown the possibility of a ‘new’ type of acid-catalysis (bifunctional catalysis by Lewis salts) in the MRH. This catalysis operates through a completely different me…

StereochemistryOrganic ChemistryIsomerization reaction MHR reaction copper(II) catalysisOxadiazoleProtonationSettore CHIM/06 - Chimica OrganicaMedicinal chemistryAdductCatalysischemistry.chemical_compoundAcid catalysischemistryMoietyPhysical and Theoretical ChemistryBifunctionalIsomerization
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A deep insight into the mechanism of the acid-catalyzed rearrangement of the Z-phenylhydrazone of 5-amino-3-benzoyl-1,2,4-oxadiazole in a non-polar s…

2010

The conversion of the Z-phenylhydrazone of 5-amino-3-benzoyl-1,2,4-oxadiazole (1a) into the relevant 1,2,3-triazole (2a) has been quantitatively studied in toluene in the presence of several halogenoacetic acids (HAAs, 3a–h). Again, the occurrence of two reaction pathways has been pointed out: they require one or two moles of acid, respectively, thus repeating the situation previously observed in the presence of trichloroacetic acid. The observed rate constant ratios (kIII/kII) are only slightly affected by the nature of the acid used. To gain a deeper insight into the action of the acids used we have measured the association constants of the HAAs (3a–h) with 4-nitroaniline (4) in toluene. …

StereochemistryOrganic ChemistryOxadiazoleSettore CHIM/06 - Chimica OrganicaTolueneMedicinal chemistrySolventchemistry.chemical_compoundAcid catalysisReaction rate constantchemistryAcid catalyzedMoleAcid catalysis azoles mononuclear rearrangement of heterocycles ring to ring interconversionPhysical and Theoretical ChemistryTrichloroacetic acidJournal of Physical Organic Chemistry
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Synthesis and preliminary antibacterial evaluation of Linezolid-like 1,2,4-oxadiazole derivatives

2012

In the present study the synthesis of new Linezolid-like molecules has been achieved by substitution of the oxazolidinone central heterocyclic moiety with a 1,2,4-oxadiazole ring. Two series of 1,2,4-oxadiazoles, bearing different side-chains and containing a varying number of fluorine atoms, were synthesized and preliminarily tested for biological activity against some Gram-positive and Gram-negative bacteria using Linezolid and Ceftriaxone as reference drugs

StereochemistryOxadiazoleMicrobial Sensitivity TestsAntimicrobial activityRing (chemistry)Oxazolidinone 124-Oxadiazole Linezolid Antimicrobial activity Fluorinated heterocyclesStructure-Activity Relationshipchemistry.chemical_compoundFluorinated heterocyclesAcetamidesDrug DiscoveryMoleculeMoiety124-OxadiazoleOxazolidinonesPharmacologyBacteriaMolecular StructureCeftriaxoneOrganic ChemistryLinezolidBiological activitySettore CHIM/06 - Chimica OrganicaGeneral MedicineSettore CHIM/08 - Chimica FarmaceuticaOxazolidinoneAnti-Bacterial AgentschemistryMED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICALinezolid
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