Search results for "Oxadiazole"

showing 10 items of 183 documents

Synthesis of fluorinated first generation starburst molecules containing a triethanolamine core and 1,2,4-oxadiazoles

2006

Abstract 5-Pentafluorophenyl-1,2,4-oxadiazoles, differently substituted at C(3), have been synthesized and used to functionalize the aliphatic primary hydroxyl functionalities of triethanolamine, under mild conditions. UV–visible absorption and emission spectra are reported, for both tri- and difunctionalised molecules, showing their potential applications as light-emitters in optoelectronic devices.

Primary (chemistry)PL spectraChemistryPl spectraOrganic Chemistry124-oxadiazolestarburst moleculeBiochemistryFirst generationfluoroarylationInorganic ChemistryTriethanolaminePolymer chemistrymedicineEnvironmental ChemistryMoleculeEmission spectrumPhysical and Theoretical ChemistryAbsorption (chemistry)medicine.drug
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Photochemistry of Fluorinated Heterocyclic Compounds. An Expedient Route for the Synthesis of Fluorinated 1,3,4-Oxadiazoles and 1,2,4-Triazoles

2004

The photochemistry of some 3-N-alkylamino-5-perfluoroalkyl-1,2,4-oxadiazoles in the presence of nitrogen nucleophiles such as ammonia and primary and secondary aliphatic amines has been investigated. The primary photolytic intermediate from the cleavage of the ring O-N bond follows two distinct and competing pathways leading to (i). 5-perfluoroalkyl-1,3,4-oxadiazoles, through the ring contraction-ring expansion photoisomerization route favored by the presence of the base or (ii). 5-perfluoroalkyl-1,2,4-triazoles, through the intervention, as an internal nucleophile, of the exocyclic N-alkylamino moiety of the oxadiazole followed by the attack of the external nitrogen nucleophile and subsequ…

RING-PHOTOISOMERIZATIONPrimary (chemistry)PhotoisomerizationFLUORO HETEROCYCLESChemistryOrganic ChemistryOxadiazoleContext (language use)Settore CHIM/06 - Chimica OrganicaRing (chemistry)Photochemistrychemistry.chemical_compoundNucleophile124-OXADIAZOLE DERIVATIVESMoiety5-MEMBERED HETEROCYCLESAliphatic compoundPHOTOINDUCED MOLECULAR-REARRANGEMENTSThe Journal of Organic Chemistry
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Ru(bpy)2Cl2: A catalyst able to shift the course of the photorearrangement in the Boulton-Katritzky reaction

2015

The Boulton-Katritzky reaction represents one of the most popular and efficient strategies used to realize azole-into-azole conversions. For example, under different experimental conditions, it allows the rearrangement of Z-arylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazoles (1) into 2-aryl-4-benzoylamino-5-phenyl-2H-1,2,3-triazoles (2) in very high yields. Moreover, we have recently realized this conversion also by UV-photostimulation. Now we have enlarged the scope of the reaction irradiating with visible or UV light an acetonitrile solution of some Z-arylhydrazones (1a-e) in the presence of catalytic amounts of Ru(bpY)(2)Cl-2. We have observed the unexpected formation of the 1-aryl-5-…

RegiochemistryRuthenium catalystDrug Discovery3003 Pharmaceutical ScienceOrganic ChemistryRegioselectivityRuthenium catalystPhotochemistryDFTBiochemistryCatalysischemistry.chemical_compoundchemistryPhotochemical rearrangementDrug Discovery124-OxadiazoleAcetonitrile
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Translational read-through as an alternative approach for ocular gene therapy of retinal dystrophies caused by in-frame nonsense mutations

2014

AbstractThe eye has become an excellent target for gene therapy, and gene augmentation therapy of inherited retinal disorders has made major progress in recent years. Nevertheless, a recent study indicated that gene augmentation intervention might not stop the progression of retinal degeneration in patients. In addition, for many genes, viral-mediated gene augmentation is currently not feasible due to gene size and limited packaging capacity of viral vectors as well as expression of various heterogeneous isoforms of the target gene. Thus, alternative gene-based strategies to stop or delay the retinal degeneration are necessary. This review focuses on an alternative pharmacologic treatment s…

Retinal degenerationGeneticsGene isoformOxadiazolesRetinal DisorderPhysiologyNonsense mutationContext (language use)Genetic TherapyBiologyBioinformaticsmedicine.diseaseSensory SystemsAminoglycosidesCodon NonsenseProtein BiosynthesisRetinal DystrophiesmedicineAnimalsHumansCoding regionGeneRetinal DystrophiesSignal TransductionVisual Neuroscience
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Readthrough Inducing Drugs (TRIDs) in human fibroblasts harboring the c.5047 C>T (R1683*) nonsense mutation

2022

Settore BIO/18 - GeneticaNonse mutationTRIDsreadthroughSettore BIO/11 - Biologia MolecolareLRBAoxadiazole
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Synthesis and chemical characterization of CuII, NiII and ZnII complexes of 3,5-bis(20-pyridyl)-1,2,4-oxadiazole and 3-(20-pyridyl)5-(phenyl)-1,2,4-o…

2011

The synthesis and structural characterization of NiII, CuII and ZnII complexes of two chelating 1,2, 4-oxadiazole ligands, namely 3,5-bis(20-pyridyl)-1,2,4-oxadiazole (bipyOXA) and 3-(20-pyridyl)5- (phenyl)-1,2,4-oxadiazole (pyOXA), is here reported. The formed hexacoordinated metal complexes are [M(bipyOXA)2(H2O)2](ClO4)2 and [M(pyOXA)2(ClO4)2], respectively (M = Ni, Cu, Zn). X-ray crystallography, 1H and 13C NMR spectroscopy and C, N, H elemental analysis data concord in attributing them an octahedral coordination geometry. The two coordinated pyOXA ligands assume a trans coplanar disposition, while the two bipyOXA ligands are not. The latter result is a possible consequence of the format…

Settore CHIM/03 - Chimica Generale E InorganicaSettore CHIM/06 - Chimica OrganicaCopper(II) complexes Crystal structure Nickel(II) complexes 124-Oxadiazoles Zinc(II) complexes
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Novel ANRORC rearrangements of 1,2,4-oxadiazoles

2010

Settore CHIM/06 - Chimica OrganicaAnrorc rearrangement oxadiazole triazole fused heterocycles
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Applications of ring rearrangements involving a participating side chain for the synthesis of five-membered heterocycles

2014

Settore CHIM/06 - Chimica OrganicaHeterocyclic rearrangements oxadiazole thiadiazole
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Sintesi e valutazione biologica di 1,2,4-ossadiazoli analoghi del Linezolid

2011

Settore CHIM/06 - Chimica Organicaoxadiazoles Linezolid anti-microbials oxazolidinonesSettore CHIM/08 - Chimica Farmaceutica
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Synthesis and biological evaluation of new 1,2,4-oxadiazole derivatives of Topsentin

Settore CHIM/08 - Chimica Farmaceutica124-oxadiazoles Topsentin Topsentin derivatives 124-oxadiazole topsentin derivatives
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