Search results for "lcsh:QD241-441"

showing 10 items of 438 documents

Highly selective generation of vanillin by anodic degradation of lignin: a combined approach of electrochemistry and product isolation by adsorption

2015

The oxidative degradation of lignin into a variety of valuable products has been under investigation since the first half of the last century. Especially, the chance to claim this cheap, abundant and renewable source for the production of the important aroma chemical vanillin (1) was one of the major driving forces of lignin research. So far most of the developed methods fail in technical application since no viable concept for work-up is included. This work represents a combined approach of electrochemical conversion of Kraft lignin and product recovery by adsorption on a strongly basic anion exchange resin. Electrolysis conditions are optimized regarding reaction temperatures below 100 °C…

ElectrolysisVanillinOrganic ChemistryligninElectrochemistryrenewable resourcesFull Research Paperlaw.inventionlcsh:QD241-441chemistry.chemical_compoundChemistrynickelAdsorptionchemistrylcsh:Organic chemistryelectrochemistrylawadsorptionDegradation (geology)LigninOrganic chemistrylcsh:QPhenolsIon-exchange resinlcsh:ScienceBeilstein Journal of Organic Chemistry
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Experimental and theoretical insights in the alkene-arene intramolecular π-stacking interaction

2016

Chiral acrylic esters derived from biomass were developed as models to have a better insight in the aryl-vinyl π-stacking interactions. Quantum chemical calculations, NMR studies and experimental evidences demonstrated the presence of equilibriums of at least four different conformations: π-stacked and face-to-edge, each of them in an s-cis/s-trans conformation. The results show that the stabilization produced by the π-π interaction makes the π-stacked conformation predominant in solution and this stabilization is slightly affected by the electron density of the aromatic counterpart. Fil: Corne, Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológi…

Electron densityStereochemistryasymmetric synthesisStackingBiomass010402 general chemistry01 natural sciencesFull Research PaperBIOMASS//purl.org/becyt/ford/1 [https]lcsh:QD241-441lcsh:Organic chemistryASYMMETRIC SYNTHESISComputational chemistryCONFORMATIONAL EQUILIBRIUMΠ-STACKING INTERACTION//purl.org/becyt/ford/1.4 [https]conformational equilibriumACRYLIC ESTERSlcsh:Sciencechemistry.chemical_classificationQuantum chemicalbiomass010405 organic chemistryAlkeneacrylic estersOtras Ciencias QuímicasOrganic ChemistryEnantioselective synthesisCiencias Químicasπ-stacking interaction0104 chemical sciencesChemistrychemistryIntramolecular forcelcsh:QCIENCIAS NATURALES Y EXACTAS
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Molecular Electron Density Theory: A Modern View of Reactivity in Organic Chemistry

2016

A new theory for the study of the reactivity in Organic Chemistry, named Molecular Electron Density Theory (MEDT), is proposed herein. MEDT is based on the idea that while the electron density distribution at the ground state is responsible for physical and chemical molecular properties, as proposed by the Density Functional Theory (DFT), the capability for changes in electron density is responsible for molecular reactivity. Within MEDT, the reactivity in Organic Chemistry is studied through a rigorous quantum chemical analysis of the changes of the electron density as well as the energies associated with these changes along the reaction path in order to understand experimental outcomes. St…

Electron densitymolecular mechanismsChemistry OrganicPharmaceutical ScienceElectronsElectron010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Electron density distributionlcsh:Organic chemistryComputational chemistryDrug DiscoveryDFT reactivity indicesNon-covalent interactionsOrganic chemistryReactivity (chemistry)Physical and Theoretical Chemistryelectron densityQuantum chemicalchemistry.chemical_classification010405 organic chemistryOrganic Chemistrymolecular electron density theory0104 chemical scienceschemistrynon-covalent interactionsModels ChemicalChemistry (miscellaneous)molecular electron density theory; DFT reactivity indices; electron localisation function; non-covalent interactions; electron density; molecular mechanisms; chemical reactivityMolecular MedicineDensity functional theoryGround stateelectron localisation functionchemical reactivityMolecules; Volume 21; Issue 10; Pages: 1319
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Understanding the Solution Behavior of Epinephrine in the Presence of Toxic Cations: A Thermodynamic Investigation in Different Experimental Conditio…

2020

The interactions of epinephrine ((R)-(&minus

EnthalpyInorganic chemistryPharmaceutical ScienceIonic bondingProtonation02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug Discoverytoxic cationSettore CHIM/01 - Chimica Analiticatoxic cationsepinephrinePhysical and Theoretical ChemistryChemistryOrganic Chemistryenthalpy and entropy changesOxidesMethylmercury Compoundsdependence on ionic strength021001 nanoscience & nanotechnologysequestering ability0104 chemical sciencesSpecific ion interaction theoryChemistry (miscellaneous)Ionic strengthBenzyl alcoholThermodynamicsUraniumMolecular MedicineTitration0210 nano-technologyenthalpy and entropy changeMolecules
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Synthesis and Structure-Activity Relationships of Amino Acid Conjugates of Cholanic Acid as Antagonists of the EphA2 Receptor

2013

The Eph–ephrin system plays a critical role in tumor growth and vascular functions during carcinogenesis. We had previously identified cholanic acid as a competitive and reversible EphA2 antagonist able to disrupt EphA2-ephrinA1 interaction and to inhibit EphA2 activation in prostate cancer cells. Herein, we report the synthesis and biological evaluation of a set of cholanic acid derivatives obtained by conjugation of its carboxyl group with a panel of naturally occurring amino acids with the aim to improve EphA2 receptor inhibition. Structure-activity relationships indicate that conjugation of cholanic acid with linear amino acids of small size leads to effective EphA2 antagonists whereas …

EphA2 antagonistsStereochemistryStructure-activity relationship studiesPharmaceutical Sciencemedicine.disease_causeArticleProtein Structure SecondaryAnalytical Chemistrylcsh:QD241-441Inhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundamino acid conjugateslcsh:Organic chemistryEphA2 anatgonistscholanic acid; amino acid conjugates; EphA2 antagonists; structure-activity relationshipsCell Line TumorDrug DiscoveryAromatic amino acidsmedicineHumansPhosphorylationPhysical and Theoretical ChemistryReceptorbile acids; EphA2 anatgonists; Structure-activity relationship studies; amino acid conjugatesbile acidschemistry.chemical_classificationBinding SitesReceptor EphA1Receptor EphA2structure-activity relationshipsOrganic ChemistryAntagonistCholic AcidsHydrogen BondingEPH receptor A2Amino acidMolecular Docking SimulationCholanic acidcholanic acidchemistryBiochemistryChemistry (miscellaneous)Molecular MedicineCarcinogenesisProtein Processing Post-TranslationalProtein BindingConjugateMolecules
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Triazolopyridines. Part 30. Hydrogen transfer reactions; pyridylcarbene formation

2013

The transfer hydrogenation reaction of (1,2,3)triaz olo(1,5-a)pyridines with Pd/C/Zn or Pd(OH) 2/C/Zn in water, ethanol or water/ethanol mixture ha s been explored. 4,5,6,7-Tetrahydro- triazolopyridines were obtained in good to medium yields. In addition, under the same conditions 2-substituted pyridines were also formed as a resul t of intermediate pyridylcarbene formation, by triazole ring opening and loss of nitrogen.

EthanolOrganic ChemistryTriazolechemistry.chemical_elementHydrogen transferRing (chemistry)Transfer hydrogenationNitrogenlcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryPolymer chemistryOrganic chemistryARKIVOC
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Grafting of Hindered Phenol Groups onto Ethylene/α-Olefin Copolymer by Nitroxide Radical Coupling

2017

The covalent immobilization of hindered phenol groups, with potential antioxidant activity, onto an ethylene/α-olefin (EOC) copolymer was carried out by the nitroxide radical coupling (NRC) reaction performed in the melt with a peroxide and the 3,5-di-tert-butyl-4-hydroxybenzoyl-2,2,6,6-tetramethylpiperidine-1-oxyl radical (BHB-T). Functionalized EOC (EOC-g-(BHB-T)) was exposed to photo- and thermo-oxidation. By comparison with some model compounds bearing the (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) moiety or the hindered phenol unit, it was observed that the grafted BHB-T could effectively help the stabilization of the polymer matrix both under photo- and thermo-oxidation. In addit…

EthylenePolymers and Plastics02 engineering and technology010402 general chemistry01 natural sciencesPeroxideArticlelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrynitroxide radical couplingPolymer chemistryCopolymerMoietyantioxidant covalent immobilizationchemistry.chemical_classificationOlefin fiberhindered phenol moietyChemistry (all)General ChemistryPolymer021001 nanoscience & nanotechnologyGrafting0104 chemical scienceschemistryCovalent bondantioxidant covalent immobilization; nitroxide radical coupling; hindered phenol moiety; HAS-NOR antioxidant0210 nano-technologyHAS-NOR antioxidantPolymers
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Methods for Determining the Thermal Transfer in Phase-Changing Materials (PCMs).

2020

A very important issue that needs to be solved as simply and correctly as possible is how to establish the thermal performance of phase-changing materials (PCM). The undertaken researches have analyzed the values of the thermal performances of the PCM taking into account the method of finite elements and the experimental research, respectively, based on a modern measurement system that was designed and implemented. Butyl stearate which has been encapsulated through complex coacervation in polymethyl methacrylate has been used as a PCM. Samples were made containing 10%, 20%, 30% and 40% PCM, respectively, within their structure. The research has established that at both the hot plate and the…

FEMMaterials sciencePolymers and Plastics020209 energyInterface (computing)System of measurementFlow (psychology)thermal transfer measurementMechanical engineeringbutyl stearate02 engineering and technologyGeneral ChemistryThermal transfer021001 nanoscience & nanotechnologyTemperature measurementFinite element methodArticlepolymethyl methacrilatlcsh:QD241-441lcsh:Organic chemistryPhase (matter)PCMThermal0202 electrical engineering electronic engineering information engineering0210 nano-technologyPolymers
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Recovery of oil with unsaturated fatty acids and polyphenols from chaenomelessinensis (Thouin) Koehne: Process optimization of pilot-scale subcritica…

2017

The potential effects of three modern extraction technologies (cold-pressing, microwaves and subcritical fluids) on the recovery of oil from Chaenomelessinensis (Thouin) Koehne seeds have been evaluated and compared to those of conventional chemical extraction methods (Soxhlet extraction). This oil contains unsaturated fatty acids and polyphenols. Subcritical fluid extraction (SbFE) provided the highest yield—25.79 g oil/100 g dry seeds—of the three methods. Moreover, the fatty acid composition in the oil samples was analysed using gas chromatography–mass spectrometry. This analysis showed that the percentages of monounsaturated (46.61%), and polyunsaturated fatty acids (42.14%), after appl…

FlavonoidPharmaceutical ScienceMass spectrometry01 natural sciencesGas Chromatography-Mass SpectrometryArticleAnalytical Chemistrylcsh:QD241-4410404 agricultural biotechnologylcsh:Organic chemistryResponse surface methodologyDrug DiscoveryPlant OilsProcess optimizationPhysical and Theoretical Chemistry<i>Chaenomelessinensis</i> (Thouin) Koehne seed oil; subcritical fluid extraction; response surface methodology; fatty acid composition; polyphenol contentMicrowavesRosaceaeChaenomelessinensis (Thouin) Koehne seed oil; Fatty acid composition; Polyphenol content; Response surface methodology; Subcritical fluid extraction; Organic Chemistrychemistry.chemical_classificationChromatography010405 organic chemistryPolyphenol contentExtraction (chemistry)Organic ChemistryPilot scalePolyphenols04 agricultural and veterinary sciences040401 food scienceChaenomelessinensis (Thouin) Koehne seed oil0104 chemical scienceschemistryChemistry (miscellaneous)PolyphenolFatty Acids UnsaturatedMolecular MedicineFatty acid compositionFatty acid compositionSubcritical fluid extractionPolyunsaturated fatty acid
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Synthesis of No-Carrier-Added 4-[18F]Fluorophenol from 4-Benzyloxyphenyl-(2-thienyl)iodonium Bromide

2011

4-[(18)F]Fluorophenol is a versatile synthon for the synthesis of more complex radiopharmaceuticals bearing a 4-[(18)F]fluorophenoxy moiety. In order to prepare 4-[(18)F]fluorophenol in no-carrier-added (n.c.a.) form only a nucleophilic labelling method starting from [(18)F]fluoride is suitable. In this paper a new, two step radiosynthesis starting from 4-benzyloxyphenyl-(2-thienyl)iodonium bromide and [(18)F]fluoride with subsequent deprotection is described, yielding n.c.a. [(18)F]fluorophenol in 34 to 36% radiochemical yield.

Fluorine Radioisotopespositron emission tomographyTwo stepNo carrier addedPharmaceutical ScienceThiophenesMedicinal chemistryAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundOnium CompoundsPhenolsNucleophilelcsh:Organic chemistryBromideDrug DiscoveryMoietyOrganic chemistryPhysical and Theoretical Chemistrydiaryl iodonium saltsCommunicationOrganic ChemistrySynthonRadiosynthesischemistryChemistry (miscellaneous)fluorine-18Molecular MedicineradiosynthesisRadiopharmaceuticalsFluoride4-[18F]fluorophenolMolecules
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