Search results for " alcoholysis"

showing 3 items of 3 documents

Ionic Liquid Gels: Supramolecular Reaction Media for the Alcoholysis of Anhydrides.

2019

The search of new enantioselective catalysts, able to promote synthetically useful organic reactions with high levels of asymmetric induction, should be associated with the attention to the suitable reaction medium able to achieve the best efficiency in chemical processes. We have investigated the enantioselective desymmetrization of cyclic meso-anhydrides in nonconventional reaction media such as ionic liquids and supramolecular gels. With this aim, we examined several variables in the reacting system: the nature of ionic liquid used as the reaction medium, the gelation solvent, the structure of the anhydrides, the structure of alcohols, the chiral catalysts, and the reaction conditions, i…

010405 organic chemistryOrganic ChemistrySupramolecular chemistryEnantioselective synthesisOrganic Chemistry supramolecular gels catalysis010402 general chemistry01 natural sciencesAsymmetric induction0104 chemical sciencesCatalysischemistry.chemical_compoundionogelsupramolecular gelchemistryOrganic reactionionic liquid ionogel supramolecular gel quinidine organocatalyst asymmetric alcoholysis of cyclic anhydrideIonic liquidOrganic chemistryquinidine organocatalystionic liquidasymmetric alcoholysis of cyclic anhydrideThe Journal of organic chemistry
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Renewable polyol obtained by microwave-assisted alcoholysis of epoxidized soybean oil: Preparation, thermal properties and relaxation process

2019

[EN] The soybean oil polyol (SOP) use as feedstock in the polyurethane industry has been recently emphasized due to its excellent resistance to hydrolysis, which is also applicable in coatings and thermal insulation. In this article, the SOP was obtained by a very fast microwave-assisted alcoholysis of epoxidized soybean oil (ESO). The preparation method, thermal properties, and relaxation process were evaluated. High yields as opening and consumption epoxy group and selectivity of 99.8 mol%, 985 mol%, and 71.2 mol% were obtained. Through titrations, nuclear magnetic resonance and gel permeation chromatography were identified parameters as 0.32 mg KOH.g(-1) acid number, 190 mg KOH.g(-1) hyd…

Acid valuefood.ingredientMaterials scienceThermal properties02 engineering and technologyDielectric relaxation spectroscopy010402 general chemistry01 natural sciencesSoybean oilGel permeation chromatographychemistry.chemical_compoundfoodMaterials Chemistry13.- Tomar medidas urgentes para combatir el cambio climático y sus efectosPhysical and Theoretical ChemistrySoybean oil polyolSpectroscopyPolyurethane021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materials02.- Poner fin al hambre conseguir la seguridad alimentaria y una mejor nutrición y promover la agricultura sostenibleEpoxidized soybean oil08.- Fomentar el crecimiento económico sostenido inclusivo y sostenible el empleo pleno y productivo y el trabajo decente para todos12.- Garantizar las pautas de consumo y de producción sostenibles07.- Asegurar el acceso a energías asequibles fiables sostenibles y modernas para todosChemical engineeringchemistryHydroxyl valueMAQUINAS Y MOTORES TERMICOS0210 nano-technologyGlass transitionMicrowave-assisted alcoholysisSaponification
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Lipase-catalysed preparation of acyl derivatives of the germacranolide sesquiterpenoid cnicin

2009

Several acyl derivatives of cnicin were obtained through lipase-catalysed acylation and alcoholysis reactions. In most reactions lipases showed a regioselective behaviour affording only one product. Longer chain acyl derivatives were prepared at lower temperature than the used in lipase-catalysed reactions, to preclude side products formation. The enzymatic approach let to prepare a family of novel acetyl and fatty acid derivatives of cnicin which are not obtainable following traditional organic synthetic procedures.

enzyme catalysis acylation alcoholysis sesquiterpenoids cnicinSettore CHIM/06 - Chimica Organica
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