Search results for "Esterification reaction"

showing 7 items of 7 documents

Direct HPLC Monitoring of Lipase Activity in Reverse Micellar Media

1995

Given the profusion of biotechnological applications of the nonaqueous use of lipases, we have evaluated the possibilities of exploiting the inherent advantages of high performance liquid chromatography (HPLC) for a simple, rapid assay of lipase activity in reverse micellar media, as a convenient alternative to previously reported spectroscopic methods, using both a model system and esterification reaction, and different commercial lipases. The results obtained after a screening for optimized chromatographic conditions in the reverse-phase mode indicate that a satisfactory resolution of the reaction components can be obtained following a straightforward protocol, which permits an accurate, …

Carboxylic Ester HydrolasesChromatographybiologyResolution (mass spectrometry)ChemistryRapid assaybiology.proteinTriacylglycerol lipaseMolecular MedicineModel systemEsterification reactionLipaseHigh-performance liquid chromatographyJournal of Liquid Chromatography
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Cutinases: Characteristics and Insights in Industrial Production

2021

Cutinases (EC 3.1.1.74) are serin esterases that belong to the α/β hydrolases superfamily and present in the Ser-His-Asp catalytic triad. They show characteristics between esterases and lipases. These enzymes hydrolyze esters and triacylglycerols and catalyze esterification and transesterification reactions. Cutinases are synthesize by plant pathogenic fungi, but some bacteria and plants have been found to produce cutinases as well. In nature they facilitate a pathogen’s invasion by hydrolyzing the cuticle that protects plants, but can be also used for saprophytic fungi as a way to nourish themselves. Cutinases can hydrolyze a wide range of substrates like esters, polyesters, triacylglycero…

CutinasepurificationeducationCutinTP1-1185behavioral disciplines and activitiesCatalysisReaccions químiquesHydrolysisdetergentCatalytic triadPhysical and Theoretical ChemistryaromasQD1-999cutinasechemistry.chemical_classificationbiologytextileChemistryChemical technologyfungicutinfood and beveragesSUPERFAMILYbiology.organism_classificationChemistryEnzymeBiochemistryEnzimsTransesterification reactionBacteriaCatalysts
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PET/PEN Blends of Industrial Interest as Barrier Materials. Part I. Many-Scale Molecular Modeling of PET/PEN Blends

2006

Mesoscale molecular simulations, based on parameters obtained through atomistic molecular dynamics and Monte Carlo calculations, have been used for modeling and predicting the behavior of PET/PEN blends. Different simulations have been performed in order to study and compare pure homopolymer blends with blends characterized by the presence of PET/PEN block copolymers acting as compatibilizer. A many-scale molecular modeling strategy was devised to evaluate PET/PEN blend characteristics, simulate phase segregation in pure PET/PEN blends, and demonstrate the improvement of miscibility due to the presence of the transesterification reaction products. The behavior of distribution densities and …

Materials sciencePolymers and Plasticsmolecular modelingOrganic ChemistryMonte Carlo methodPET/PEN blends Many-scale molecular modeling Transesterification reactionThermal diffusivityblendMiscibilityMolecular dynamicsPETPENPhase (matter)Materials ChemistryCopolymerOrganic chemistryGaseous diffusionPolymer blendComposite material
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ChemInform Abstract: Selective Formal Transesterification of Fluorinated 2-(Trimethylsilyl)ethyl α-Imino Esters Mediated by TBAF.

2008

The scope of the transesterification reaction between β-fluorinated α-imino esters and various electrophiles in the presence of TBAF as fluorine source is described. The reaction is highly selective for alkyl iodides, bromides, and mesylates, while alkyl chlorides react at a significantly slower rate and tosylates do not react under the reaction conditions. This methodology represents a simple and useful alternative for the preparation of a wide variety of fluorinated α-imino esters.

Reaction conditionschemistry.chemical_classificationTrimethylsilylchemistry.chemical_elementGeneral MedicineTransesterificationHighly selectivechemistry.chemical_compoundchemistryElectrophileFluorineOrganic chemistryheterocyclic compoundsTransesterification reactionAlkylChemInform
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Asymmetric synthesis of functionalized tetrahydrofluorenones via an NHC-catalyzed homoenolate Michael addition

2018

The first example of an N-heterocyclic carbene-catalyzed asymmetric desymmetrization of enal-tethered cyclohexadienones via an intramolecular homoenolate Michael addition/esterification reaction is described. This new protocol offers a direct entry to various functionalized tetrahydrofluorenones with three contiguous stereocenters in high yields, good diastereoselectivities and excellent enantioselectivities.

aromaattiset yhdisteet010402 general chemistry01 natural sciencesDesymmetrizationCatalysisStereocenterCatalysisDirect entryMaterials Chemistryta116kemiallinen synteesi010405 organic chemistryChemistryaromatic compoundsMetals and AlloysEnantioselective synthesisGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIntramolecular forceCeramics and CompositesMichael reactionEsterification reactionchemical synthesisChemical Communications
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Ultrasound accelerated esterification of bile acids

2004

In this study power ultrasound accelerated esterification reactions of some model substances and bile acids were done. In the model reactions the best result was 19-fold increase in the reaction rate when using ultrasound and the temperature was allowed to rise during the irradiation. In the case of bile acid methyl esters a clear increase in the reaction rates was also observed by ultrasonic irradiations.

bile acidsChromatographyAcoustics and UltrasonicsBile acidultrasoundChemistrybusiness.industrymedicine.drug_classesterificationOrganic ChemistryUltrasoundultrasound treatmentInorganic ChemistryReaction rateesterification reactionspower ultrasoundmedicineChemical Engineering (miscellaneous)Environmental ChemistryOrganic chemistryRadiology Nuclear Medicine and imagingUltrasonic sensorIrradiationbusinessUltrasonics Sonochemistry
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Catalytic Activity of Char Obtained from Fast Pyrolysis in Esterification Reactions

2021

In this study different pathways for obtaining activated carbon with catalytical activity were analysed. Industrially fast pyrolysis is an efficient way of lignocellulosic biomass processing, since in this process various important high value chemicals are obtained. Biochar is obtained as the by-product in fast pyrolysis process from which activated carbon can be acquired with further chemical activation. Different methods for chemical activation of biochar were tested with the obtained activated charcoals being used as a catalyst in esterification reactions to evaluate their potential use as a heterogenic catalyst. Highest catalytical activity was observed when biochar was pre-treated with…

inorganic chemicalsMaterials science020209 energyLignocellulosic biomass02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsCatalysis0202 electrical engineering electronic engineering information engineeringOrganic chemistryGeneral Materials ScienceEsterification reactionChar0210 nano-technologyPyrolysisSolid State Phenomena
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