Search results for "Benzaldehyde"

showing 10 items of 112 documents

Selective photooxidation of ortho-substituted benzyl alcohols and the catalytic role of ortho-methoxybenzaldehyde

2016

It has been recently reported by Palmisano et al. (2015) [1] that the oxidation of 2-methoxybenzyl alcohol (2-MBA) to 2-methoxybenzaldehyde (2-MBAD) proceeds in water under near-UV light with an unexpected catalytic effect of 2-MBAD. In order to investigate the catalytic role of aldehyde in photolytic oxidation of ortho-substituted benzyl alcohols (OSBAs), reactivity runs were carried out with 2-methylbenzyl alcohol (2-MeBA), 2-nitrobenzyl alcohol (2-NBA), 2-hydroxybenzyl alcohol (2-HBA) and 2-chlorobenzyl alcohol (2-CIBA) in the absence and in the presence of their corresponding aldehyde. None of those alcohols showed a measurable oxidation rate even in the presence of their aldehydes but …

General Chemical EngineeringGeneral Physics and AstronomyAlcohol2-MethoxybenzaldehydeHomogeneous photocatalysi010402 general chemistry01 natural sciencesAldehydeCatalysisFerulic acidPhysics and Astronomy (all)chemistry.chemical_compoundBenzyl alcoholOrganic chemistryChemical Engineering (all)Reactivity (chemistry)chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria Chimica010405 organic chemistryChemistryChemistry (all)General Chemistry0104 chemical sciencesAutocatalytic photooxidationAlcohol oxidationPhotocatalysis2-Methoxybenzaldehyde; Autocatalytic photooxidation; Benzyl alcohols; Homogeneous photocatalysis; Chemistry (all); Chemical Engineering (all); Physics and Astronomy (all)Selectivity
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Chemical composition and biological activity of Salvia verbenaca essential oil

2011

Salvia verbenaca L. (syn. S. minore) is a perennial herb known in the traditional medicine of Sicily as “spaccapetri” and is used to resolve cases of kidney stones, chewing the fresh leaves or in decoction. The chemical composition of the essential oil obtained from aerial parts of S. verbenaca collected in Piano Battaglia (Sicily) on July 2009, was analyzed by GC and GC-MS. The oil was strongly characterized by fatty acids (39.5%) and carbonylic compounds (21.2%), with hexadecanoic acid (23.1%), ( Z)-9-octadecenoic acid (11.1%) and benzaldehyde (7.3%) as the main constituents. The in vitro activity of the essential oil against some microorganisms in comparison with chloramphenicol by the …

Gram-positive bacteriaCarboxylic AcidsDecoctionMicrobial Sensitivity TestsPlant ScienceSalviaGram-Positive BacteriaGas Chromatography-Mass Spectrometrylaw.inventionfoodlaw(Z)-9-octadecenoic acidGram-Negative BacteriaDrug DiscoveryPlant OilsVolatile componeSettore BIO/15 - Biologia FarmaceuticaSalviaFood scienceSicilyChemical compositionEssential oilPharmacologyβ-phellandrene (Z)-9-octadecenoic acid Antibacterial activity Benzaldehyde Hexadecanoic acid Lamiaceae Salvia verbenaca Volatile componeLamiaceaeSalvia verbenacabiologyChemistryFatty AcidsVolatile componentsSettore CHIM/06 - Chimica OrganicaGeneral MedicineBenzaldehydePlant Components Aerialbiology.organism_classificationfood.foodAnti-Bacterial AgentsComplementary and alternative medicineβ-phellandreneSalvia verbenacaAntibacterial activityGas chromatography–mass spectrometryHexadecanoic acidBacteria
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Comparative cytotoxic study of silica materials functionalised with essential oil components in HepG2 cells

2020

[EN] This work evaluated the cytotoxic effect of different EOCs-functionalised silica particle types. The in vitro toxicity of eugenol and vanillin-immobilised SAS, MCM-41 microparticles and MCM-41 nanoparticles was evaluated on HepG2 cells, and compared to free EOCs and pristine materials. The results revealed that free essential oil components and bare silica had a mild cytotoxic effect on HepG2 cells. However, the comparative study showed that free eugenol and vanillin had a milder cytotoxic effect than the equivalent concentrations of immobilised components on the different silica particles, while differences in cell viability between the bare and functionalised particles relied on the …

HepG2TECNOLOGIA DE ALIMENTOSCell SurvivalCytotoxicityNanoparticleToxicologyMCM-41law.invention03 medical and health scienceschemistry.chemical_compoundInhibitory Concentration 500404 agricultural biotechnologyMCM-41Microscopy Electron TransmissionlawEugenolOils VolatileCytotoxic T cellHumansCytotoxicityEssential oil030304 developmental biology0303 health sciencesDose-Response Relationship DrugVanillinCationic polymerizationSilica04 agricultural and veterinary sciencesGeneral MedicineHep G2 CellsSilicon Dioxide040401 food scienceEugenolchemistryBenzaldehydesVanillinNanoparticlesFood ScienceNuclear chemistry
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Ionic liquids as solvents for the Knoevenagel condensation: understanding the role of solvent–solute interactions

2015

The Knoevenagel condensation in ionic liquids has been demonstrated as a strongly solvent-dependent process. The objective of this study was to establish a simple and descriptive trend of solvent–solute interactions that favour the Knoevenagel condensation in ionic liquid media. The reaction between 4-(dimethylamino)benzaldehyde and ethyl cyanoacetate in several imidazolium- and pyrrolidinium-based ionic liquids and one ionic liquid mixture was studied. The rate constants were rationalised by studying the change in the 1H NMR chemical shift of representative starting materials in the ionic liquids and the measurement and consideration of the Kamlet–Taft descriptors for each solvent. The hyd…

Hydrogen bondChemistryGeneral ChemistryCatalysisSolventBenzaldehydechemistry.chemical_compoundReaction rate constantEthyl cyanoacetateIonic liquidMaterials ChemistryProton NMROrganic chemistryKnoevenagel condensationNew Journal of Chemistry
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Diorganotin Compounds Containing α‐Aminoacidato Schiff Base Ligands Derived from Functionalized 2‐Hydroxy‐5‐(aryldiazenyl)benzaldehyde. Syntheses, St…

2020

Inorganic ChemistryBenzaldehydechemistry.chemical_compoundSchiff basechemistryHydrogen sulfidePolymer chemistrychemistry.chemical_elementTinEuropean Journal of Inorganic Chemistry
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Liquid phase selective oxidation of benzyl alcohol over Pd–Ag catalysts supported on pumice

2001

Abstract Selective oxidation of benzyl alcohol to benzaldehyde was carried out over pumice supported bimetallic and monometallic Pd and Ag catalysts. Preliminary kinetic studies were performed at 333 K in autoclave, at pressure of 2 atm in pure oxygen. Under these conditions, small amounts of benzoic acid were detected with the monometallic Pd pumice being the most active catalyst. The reaction was also carried out under flowing oxygen at atmospheric pressure and at 348 K. Under these conditions, the selectivity to benzaldehyde was 100%. The catalytic activity of the catalysts was measured after different oxidation and reduction treatments at high temperature. In addition, two mechanical mi…

Inorganic chemistrychemistry.chemical_elementGeneral ChemistryHeterogeneous catalysisCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryTransition metalBenzyl alcoholBimetallic stripBenzoic acidPalladiumCatalysis Today
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Vanillin Suppresses Metastatic Potential of Human Cancer Cells through PI3K Inhibition and Decreases Angiogenesis in Vivo

2009

Vanillin, a food flavoring agent, has been shown to suppress cancer cell migration and metastasis in a mouse model, but its mechanism of action is unknown. In this report, we have examined the antimetastatic potential of vanillin and its structurally related compounds, vanillic acid, vanillyl alcohol, and apocynin on hepatocyte growth factor (HGF)-induced migration of human lung cancer cells by the Transwell assay. Vanillin and apocynin could inhibit cell migration, and both compounds selectively inhibited Akt phosphorylation of HGF signaling, without affecting phosphorylation of Met and Erk. Vanillin and apocynin could inhibit the enzymatic activity of phosphoinositide 3-kinase (PI3K), as …

Lung NeoplasmsAngiogenesisAdenocarcinomaPharmacologyVanillyl alcoholchemistry.chemical_compoundCell MovementCell Line TumormedicineVanillic acidHumansEnzyme InhibitorsNeoplasm MetastasisPhosphoinositide-3 Kinase InhibitorsNeovascularization PathologicHepatocyte Growth FactorKinaseVanillinAcetophenonesGeneral ChemistrychemistryMechanism of actionBiochemistryBenzaldehydesApocyninHepatocyte growth factormedicine.symptomGeneral Agricultural and Biological SciencesSignal Transductionmedicine.drugJournal of Agricultural and Food Chemistry
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Tuning the photocatalytic activity of bismuth wolframate: Towards selective oxidations for the biorefinery driven by solar-light

2017

The sol–gel entrapment of nanostructured Bi2WO6 enhances the activity and the selectivity of the short-gap semiconductor in the sunlight-driven photo-oxidation of trans-ferulic and trans-cinnamic acid dissolved in water with air as the primary oxidant. Valuable products such as vanillin, benzaldehyde, benzoic acid and vanillic acid are obtained. This provides the proof of concept that photocatalysis could be a promising technology in tomorrow's solar biorefineries.

Materials Chemistry2506 Metals and AlloysNanostructureSurfaces Coatings and Film02 engineering and technologyCoumaric Acid01 natural sciencessolar-lightBismuthCatalysichemistry.chemical_compoundMaterials ChemistryBenzoic acidMolecular StructureElectronic Optical and Magnetic MaterialChemistry (all)Metals and AlloysTungsten CompoundsBenzoic Acid021001 nanoscience & nanotechnologyPhotochemical ProcessesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBenzaldehydesPhotocatalysisSunlight0210 nano-technologySelectivityOxidation-ReductionCoumaric AcidsInorganic chemistrychemistry.chemical_elementCeramics and Compositebismuth wolframate010402 general chemistryCatalysisTungstenBenzaldehydePhotochemical ProcesseCinnamateVanillic acidsol-gelsolar biorefineriesselective reactionsVanillic Acidgreen chemistryVanillinWaterGeneral ChemistryBenzaldehydeBiorefinery0104 chemical sciencesNanostructureschemistryChemical engineeringTungsten CompoundCinnamatesCeramics and CompositesSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie2506photocatalysisBismuth
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Diaqua[5,10,15,20-tetrakis(4-chlorophenyl)porphyrinato-κ4N]iron(III) trifluoromethanesulfonate–4-hydroxy-3-methoxybenzaldehyde–water (1/1/2)

2014

In the title compound, [Fe(C44H24Cl4N4)(H2O)2](SO3CF3)·C8H8O3·2H2O, the FeIIIcation is chelated by the four N atoms of the deprotonated tetrakis(4-chlorotetraphenyl)porphyrin (TClPP) and further coordinated by two water molecules in a distorted octahedral geometry. In the crystal, the cations, anions, 4-hydroxy-3-methoxybenzaldehyde and water molecules of crystallization are linked by classical O—H...O hydrogen bonds and weak C—H...O and C—H...Cl hydrogen bonds into a three-dimensional supramolecular architecture. The crystal packing is further stabilized by weak C—H...π interactions involving pyrrole and benzene rings. π–π stacking between parallel benzene rings of adjacent 4-hydroxy-3-met…

Metal-Organic Paperscrystal structureHydrogen bondMethane sulfonateGeneral ChemistryCrystal structureCondensed Matter PhysicsBioinformaticsMedicinal chemistryPorphyrinlaw.inventionBenzaldehydelcsh:Chemistrychemistry.chemical_compoundDeprotonationchemistrylcsh:QD1-999lawGeneral Materials ScienceCrystallizationPyrroleActa Crystallographica Section E
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A Modular Access to (±)-Tubocurine and (±)-Curine - Formal Total Synthesis of Tubocurarine.

2017

Two consecutive Cu-catalyzed Ullmann-type C–O couplings permitted the first successful entry toward the curare alkaloids (±)-tubocurine and (±)-curine. Starting from vanillin, the synthetic sequence comprises 15 linear steps and includes a total of 24 transformations. In addition, the total synthesis of tubocurine represents a formal total synthesis of the famous arrow poison alkaloid tubocurarine.

Molecular Structure010405 organic chemistryStereochemistryChemistryAlkaloidOrganic ChemistryCurare alkaloidsChemistry OrganicTotal synthesisTubocurarine010402 general chemistryIsoquinolines01 natural sciencesCatalysis0104 chemical sciencesTubocurineBenzaldehydesCopperThe Journal of organic chemistry
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