Search results for "Azides"

showing 10 items of 67 documents

Cellulose‑copper as bio-supported recyclable catalyst for the clickable azide-alkyne [3 + 2] cycloaddition reaction in water.

2018

Abstract Naturally-occurring cellulose has been employed as a bio-support macromolecule for the immobilization of either copper(I) or copper(II) ions in order to click azide and alkyne derivatives in water. Under such a click regime, 1,4-disubstitued-1,2,3-triazoles were obtained regioselectively in excellent yields at room temperature. The reaction work-up is simple and the bio-heterogeneous catalyst that has been fully characterized by AAS, SEM, EDX and FT-IR can be easily separated and reused at least five times without any significant decrease in its activity and selectivity, particularly in the case of the very stable CuI-Cellulose.

Azides123-TriazoleAlkynechemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysischemistry.chemical_compoundStructural BiologyPolymer chemistrySpectroscopy Fourier Transform InfraredCelluloseCelluloseMolecular Biologychemistry.chemical_classificationCycloaddition Reaction010405 organic chemistryChemistryWaterGeneral MedicineCopperCycloaddition0104 chemical sciencesAlkynesClick chemistrySolventsClick ChemistryAzideCopperInternational journal of biological macromolecules
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Synthesis of aryl azides: A probe reaction to study the synergetic action of ultrasounds and ionic liquids

2011

Abstract The combined effect of ultrasounds and ionic liquids was used to perform the synthesis of aryl azides by nucleophilic aromatic substitution in ionic liquid/[1-butyl-3-methylimidazolium][N 3 ] binary mixtures. The ultrasounds efficiency was analyzed as a function of the substrate and of the ionic liquid structure. In the first case, both 6π and 10π electrons aryl halides were considered. As far as the ionic liquid structure is concerned, both aromatic and aliphatic ionic liquids were taken into account. Among aromatic cations, the effects due to different ability in giving hydrogen bond or π–π interactions were considered. The use of a geminal ionic liquid having an aromatic spacer …

AzidesAcoustics and UltrasonicsInorganic chemistryIonic LiquidsHalideChemistry Techniques SyntheticPhotochemistryIonInorganic Chemistrychemistry.chemical_compoundNucleophilic aromatic substitutionChemical Engineering (miscellaneous)Environmental ChemistryUltrasonicsRadiology Nuclear Medicine and imagingMolecular StructureGeminalHydrogen bondArylOrganic ChemistrySubstrate (chemistry)StereoisomerismSettore CHIM/06 - Chimica OrganicachemistryIonic liquidIonic liquids Ultrasounds Aryl azides Nucleophilic aromatic substitutionUltrasonics Sonochemistry
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The characterization of molecular alkaly metal azides

2006

Matrix isolation infrared (IR) studies have been carried out on the vaporisation of the alkali-metal azides MN(3) (M = Na, K, Rb and Cs). The results show that under high vacuum conditions, molecular KN(3), RbN(3) and CsN(3) are present as stable high-temperature vapour species, together with variable amounts of nitrogen gas and the corresponding metal atoms. The characterisation of these molecular azides is supported by ab initio molecular orbital calculations and density functional theory (DFT) calculations, and for CsN(3) in particular, by the detection of the isotopomers CS((14)N(15)N(14)N) and Cs((15)N(14)N(14)N). The IR spectra are assigned to a "side-on" (C(2v)) structure by comparis…

AzidesAlkali metalsInfraredChemistryOrganic ChemistryMatrix isolationAb initioAnalytical chemistryInfrared spectroscopyTheoretical calculationsGeneral ChemistryMatrix isolationCatalysisIsotopomersIR spectroscopyddc:540AtomCASSCF azides single moleculeDensity functional theoryMolecular orbital
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Spacer-separated sialyl LewisX cyclopeptide conjugates as potential E-selectin ligands.

2006

Completely protected sialyl LewisX azide was synthesized from a neolactosamine azide precursor carrying a 3-O-allyloxycarbonyl group as the temporary protecting group. After its Pd(0)-catalyzed deprotection and stereoselective alpha-fucosylation, the obtained LewisX azide was subjected to O-deacetylation in the galactose unit and subsequent regio- and stereoselective sialylation. Reduction of the anomeric azido group afforded the sialyl LewisX amine building block. Two molecules of this tetrasaccharide ligand were conjugated to a preformed cyclooctapeptide containing two equidistant l-asparagine units equipped with carboxy-terminated tetraethyleneglycol side chains to give, after deprotecti…

AzidesAnomerStereochemistryNeutrophilsOligosaccharidesConjugated systemLigandsBiochemistryPeptides CyclicAnalytical Chemistrychemistry.chemical_compoundMiceLewis Blood Group AntigensTetrasaccharideAnimalsProtecting groupSialyl Lewis X AntigenLigandOrganic ChemistryGlycopeptidesGeneral MedicinechemistryAmine gas treatingAzideE-SelectinConjugateCarbohydrate research
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A combined experimental and theoretical study of the thermal cycloaddition of aryl azides with activated alkenes.

2011

International audience; Reactions were performed from aryl azides on the one hand, and activated alkenes coming from β-dicarbonyl compounds or malonodinitrile on the other hand, either with recourse to conventional heating or to microwave activation, to afford 1-aryl-1H-1,2,3-triazoles. The mechanism and the regioselectivity of the reactions involving β-dicarbonyl compounds have been theoretically studied using DFT methods at the B3LYP/6-31G* level: they are domino processes comprising a tautomeric equilibrium of the β-dicarbonyl compounds with their enol forms, a 1,3-dipolar cycloaddition of the enol forms with the aryl azides (high activation energy), and a dehydration process (lower acti…

AzidesAntifungal AgentsAntineoplastic AgentsMicrobial Sensitivity TestsActivation energyAlkenes010402 general chemistryPhotochemistry01 natural sciencesBiochemistryStructure-Activity Relationshipchemistry.chemical_compoundCell Line TumorThermalHumansPhysical and Theoretical ChemistryMicrowavesMolecular Structure010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryArylOrganic ChemistryTemperatureRegioselectivityStereoisomerismTriazolesEnolCombinatorial chemistryTautomerCycloadditionAnti-Bacterial Agents0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryCyclizationQuantum TheoryDegradation (geology)Drug Screening Assays Antitumor
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Application of propidium monoazide-qPCR to evaluate the ultrasonic inactivation of Escherichia coli O157:H7 in fresh-cut vegetable wash water.

2012

The efficacy of sanitizing technologies in produce or in vegetable wash water is generally evaluated by plate count in selective media. This procedure is time consuming and can lead to misinterpretations because environmental conditions and sanitizing processes may affect bacterial growth or culturable capability. Thus, the aim of this study was to determine the applicability of a propidium monoazide real-time PCR (PMA-qPCR) method to monitor the inactivation by ultrasound treatment of foodborne bacteria in fresh-cut vegetable wash water. To this aim, lettuce wash water was artificially inoculated with Escherichia coli O157:H7 (10⁶ CFU/mL) and treated by means of a continuous ultrasonic irr…

AzidesCell SurvivalFood HandlingColony Count MicrobialFood ContaminationBiologyBacterial growthmedicine.disease_causeEscherichia coli O157Real-Time Polymerase Chain ReactionMicrobiologyMicrobiologyPropidium monoazideVegetablesmedicineFood scienceEscherichia coliDetection limitFoodborne bacteriabiology.organism_classificationDisinfectionWash waterConsumer Product SafetyFood MicrobiologyUltrasonic sensorBacteriaFood SciencePropidiumFood microbiology
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Recent advances in copper-based solid heterogeneous catalysts for azide-alkyne cycloaddition reactions

2022

The copper(I)-catalyzed azide−alkyne cycloaddition (CuAAC) reaction is considered to be the most representative ligation process within the context of the “click chemistry” concept. This CuAAC reaction, which yields compounds containing a 1,2,3-triazole core, has become relevant in the construction of biologically complex systems, bioconjugation strategies, and supramolecular and material sciences. Although many CuAAC reactions are performed under homogenous conditions, heterogenous copper-based catalytic systems are gaining exponential interest, relying on the easy removal, recovery, and reusability of catalytically copper species. The present review covers the most recently developed copp…

AzidesCycloaddition ReactionOrganic ChemistryGeneral MedicineQuímicaTriazolesCatalysisComputer Science ApplicationsInorganic ChemistryAlkynesClick ChemistryPhysical and Theoretical ChemistryMolecular BiologyCopperSpectroscopy
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The inhibition of Ca2+-ATPases of human erythrocyte membranes by covalent binding of ATP derivatives.

1982

AzidesErythrocytesChemistryUltraviolet RaysGeneral NeuroscienceErythrocyte MembraneCovalent bindingBiological Transport ActiveCa2 atpasesCalcium-Transporting ATPasesGeneral Biochemistry Genetics and Molecular BiologyKineticsMembraneAdenosine TriphosphateHistory and Philosophy of ScienceBiophysicsHumansEthenoadenosine TriphosphateProtein BindingAnnals of the New York Academy of Sciences
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Application of viability PCR to discriminate the infectivity of hepatitis A virus in food samples.

2015

Abstract Transmitted through the fecal–oral route, the hepatitis A virus (HAV) is acquired primarily through close personal contact and foodborne transmission. HAV detection in food is mainly carried out by quantitative RT-PCR (RT-qPCR). The discrimination of infectious and inactivated viruses remains a key obstacle when using RT-qPCR to quantify enteric viruses in food samples. Initially, viability dyes, propidium monoazide (PMA) and ethidium monoazide (EMA), were evaluated for the detection and quantification of infectious HAV in lettuce wash water. Results showed that PMA combined with 0.5% Triton X-100 (Triton) was the best pretreatment to assess HAV infectivity and completely eliminate…

AzidesHot TemperatureOctoxynolvirusesReal-Time Polymerase Chain ReactionMicrobiologyVirusMicrobiologyCell LinePropidium monoazideVegetablesAnimalsShellfishInfectivityMicrobial ViabilitybiologyInoculationvirus diseasesGeneral MedicineHepatitis Abiology.organism_classificationHepatitis a virusBivalviaReal-time polymerase chain reactionFood MicrobiologySpinachRNA ViralVirus InactivationIndicators and ReagentsHepatitis A virusFood SciencePropidiumInternational journal of food microbiology
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Direct subphthalocyanine conjugation to bombesin vs. indirect conjugation to its lipidic nanocarrier

2016

International audience; Bombesin (BBN) was covalently bound to graftable subphthalocyanine (SubPc) or to a cholesterol derivative, a component of a liposome that encapsulates non-graftable SubPc. The latter bioconjugation approach was suitable to address the stability of SubPc and was achieved by copper-free click-chemistry on the outer-face of the liposome. Liposomes were purified (FPLC) and then analyzed in size (outer diameter about 60 nm measured by DLS). In vitro binding studies allowed to determine the IC50 13.9 nM for one component of the liposome, cholesterol, conjugated to BBN. Hence, azido- (or alkynyl-) liposomes give fluorophores with no reactive functional group available on th…

AzidesIndolesStereochemistryefficacyConjugated systemIsoindoles010402 general chemistry01 natural sciencesBiochemistry[ CHIM ] Chemical Scienceschemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesPhysical and Theoretical Chemistrysilicon phthalocyaninesmelanoma-cellsLiposomeBioconjugationfluorescent[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryBombesinFast protein liquid chromatographyCombinatorial chemistryFluorescence0104 chemical sciencesNanostructuresmelanocyteschemistryphotodynamic therapyCovalent bondAlkynesLiposomesBombesinactivationNanocarriers
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