Search results for "Zole"

showing 10 items of 2482 documents

CCDC 705804: Experimental Crystal Structure Determination

2010

Related Article: G.Dupouy, S.Triki, M.Marchivie, N.Cosquer, C.J.Gomez-Garcia, S.Pillet, E.-E.Bendeif, C.Lecomte, S.Asthana, J.-F.Letard|2010|Inorg.Chem.|49|9358|doi:10.1021/ic101038z

catena-[(mu~2~-2-Dicyanomethylene-1133-tetracyanopropanediide-NN')-bis(4-amino-35-bis(pyridin-2-yl)-124-triazole-NN')-iron(ii)]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2011617: Experimental Crystal Structure Determination

2020

Related Article: Anna Świtlicka, Barbara Machura, Rafał Kruszynski, Nicolás Moliner, José Miguel Carbonell, Joan Cano, Francesc Lloret, Miguel Julve|2020|Inorg.Chem.Front.|7|4535|doi:10.1039/D0QI00752H

catena-[bis(mu-azido)-bis(1-benzyl-1H-imidazole)-cobalt]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1432273: Experimental Crystal Structure Determination

2016

Related Article: Anna Świtlicka-Olszewska, Joanna Palion-Gazda, Tomasz Klemens, Barbara Machura, Julia Vallejo, Joan Cano, Francesc Lloret, Miguel Julve|2016|Dalton Trans.|45|10181|doi:10.1039/C6DT01160H

catena-[bis(mu2-Dicyanamide)-bis(1-benzyl-1H-imidazole)-cobalt(ii)]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1440482: Experimental Crystal Structure Determination

2016

Related Article: Néstor Calvo Galve, Mónica Giménez-Marqués, Miguel Palomino, Susana Valencia, Fernando Rey, Guillermo Mínguez Espallargas, Eugenio Coronado|2016|Inorg.Chem.Front.|3|808|doi:10.1039/C5QI00277J

catena-[tris(mu-11'-((11'-biphenyl)-44'-diylbis(methylene))bis(1H-tetrazole))-iron bis(tetrafluoroborate)]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Design, Synthesis and Biological Evaluation of Novel Pyrazolo[1,2,4]triazolopyrimidine Derivatives as Potential Anticancer Agents

2021

Three novel pyrazolo-[4,3-e][1,2,4]triazolopyrimidine derivatives (1, 2, and 3) were designed, synthesized, and evaluated for their in vitro biological activity. All three compounds exhibited different levels of cytotoxicity against cervical and breast cancer cell lines. However, compound 1 showed the best antiproliferative activity against all tested tumor cell lines, including HCC1937 and HeLa cells, which express high levels of wild-type epidermal growth factor receptor (EGFR). Western blot analyses demonstrated that compound 1 inhibited the activation of EGFR, protein kinase B (Akt), and extracellular signal-regulated kinase (Erk)1/2 in breast and cervical cancer cells at concentrations…

cervical cancercrystal X-ray analysisPharmaceutical ScienceAntineoplastic AgentsArticleAnalytical ChemistryHeLa03 medical and health sciencesbreast cancerQD241-4410302 clinical medicineDrug DiscoveryHumansEpidermal growth factor receptorPhysical and Theoretical Chemistrypyrazolo[124]triazolopyrimidineCytotoxicityProtein Kinase InhibitorsProtein kinase BCell Proliferation030304 developmental biologyMitogen-Activated Protein Kinase 1pyrazolo[124]triazolopyrimidine; EGF-receptor inhibitor; breast cancer; cervical cancer; molecular docking; crystal X-ray analysis0303 health sciencesBinding SitesMitogen-Activated Protein Kinase 3biologyChemistryKinaseOrganic ChemistryBiological activitymolecular dockingTriazolesbiology.organism_classificationMolecular biologyIn vitroErbB ReceptorsMolecular Docking SimulationPyrimidinesChemistry (miscellaneous)Docking (molecular)030220 oncology & carcinogenesisbiology.proteinMolecular MedicineProto-Oncogene Proteins c-aktEGF-receptor inhibitorHeLa CellsProtein BindingMolecules
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Development of a Chiral DMAP Catalyst for the Dynamic Kinetic Resolution of Azole Hemiaminals

2017

A new catalyst for the dynamic kinetic resolution of azole hemiaminals has been developed using late-stage structural modifications of the tert-leucinol-derived chiral subunit of DMAP species.

chemistry.chemical_classification010405 organic chemistryChemistryOrganic ChemistryOrganic chemistryAzole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysisKinetic resolutionThe Journal of Organic Chemistry
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The First 1,3,4‐Oxadiazole Based Dinuclear Iron(II) Complexes Showing Spin Crossover Behavior with Hysteresis

2015

Three new dinuclear complexes [FeII2(μ-L)2]X4 (L is the bis-tridentate ligand 2,5-bis{[(2-pyridylmethyl)amino]methyl}-1,3,4-oxadiazole and X = ClO4–, BF4– and CF3SO3–) have been synthesized and fully characterized by single-crystal X-ray diffraction, Mossbauer spectroscopy and magnetic susceptibility measurements. Upon cooling, a trapped [high-spin–low-spin] state of the iron(II) centres is detected. Depending on the counterion, a pronounced thermal hysteresis is found. In one case, it was possible to observe a space group change that accompanies the spin transition. This is the first system showing spin crossover based on an oxadiazole ligand.

chemistry.chemical_classification010405 organic chemistryLigandInorganic chemistrySpin transitionOxadiazole010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryHysteresischemistry.chemical_compoundCrystallographychemistrySpin crossoverMössbauer spectroscopyCounterionEuropean Journal of Inorganic Chemistry
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P-Chirogenic Triazole-Based Phosphine: Synthesis, Coordination Chemistry, and Asymmetric Catalysis

2020

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryEnantioselective synthesisTriazole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCoordination complexchemistry.chemical_compoundchemistryTransition metalPhysical and Theoretical ChemistryPhosphineEuropean Journal of Organic Chemistry
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Synthesis of conformationally restricted 1,2,3-triazole-substituted ethyl β- and γ-aminocyclopentanecarboxylate stereoisomers. Multifunctionalized al…

2010

Abstract Stereoisomers of 1,2,3-triazole-functionalized, conformationally restricted β- or γ-amino esters with a cyclopentane skeleton were efficiently synthetized from the bicyclic β-lactam 6-azabicyclo[3.2.0]hept-3-en-7-one (1) and Vince γ-lactam (15) in five or six steps involving the azide–alkyne 1,3-dipolar cycloaddition of azido-substituted amino ester stereoisomers with nonsymmetric acetylenes. The azide–alkyne click reactions were investigated under thermal and Cu(I)-catalyzed conditions. Surprisingly, the thermally induced cycloaddition furnished the corresponding 1,4-triazoles regioselectively, which also took place selectively in response to Cu(I) catalysis.

chemistry.chemical_classification123-TriazoleAmino estersBicyclic moleculeStereochemistryOrganic ChemistryBiochemistryChemical synthesisCycloadditionchemistry.chemical_compoundAlicyclic compoundchemistryDrug Discovery13-Dipolar cycloadditionClick chemistryTetrahedron
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Synthesis, crystal structure and magnetic properties of bis[μ-bis(3-(pyridin-2-yl)-1,2,4-triazole-N′,N1,N2)] bis[triaqua nickel(II)] tetranitrate

1998

Abstract A new dinuclear nickel(II) coordination compound of formula Ni2(Hpt)2(H2O)6(NO3)4 (Hpt=3-(pyridin-2-yl)-1,2,4-triazole) was synthesized. The structure was solved at 298 K by single-crystal X-ray analysis. Bisμ-bis(3-(pyridin-2-yl)-1,2,4-triazole-N′,N1,N2) bistriaqua nickel(II) tetranitrate (C14H24N12O18Ni2) crystallizes in the triclinic space group P-1, a=7.2266(1), b=9.9144(1), c=11.2647(1) A, α=66.854(1)°, β=74.000(1)°, γ=86.400(2)°, V=712.42(1) A3, Z=1 (dinuclear units), 2823 reflections (1 > 2σ(I)), R1=0.0442, wR2=0.1197. The Ni(II) ions are bridged by two neutral Hpt ligands coordinating via N1 and N2 in the equatorial plane, Ni(1)-Ni(1)′=4.098(1) A. The Hpt bridging mode is a…

chemistry.chemical_classification124-Triazolechemistry.chemical_elementCrystal structureTriclinic crystal systemCoordination complexInorganic Chemistrychemistry.chemical_compoundNickelCrystallographychemistryOctahedronSuperexchangeMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
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