Search results for "ACYLATION"

showing 7 items of 87 documents

Susceptibility of Methyl 3-Amino-1H-pyrazole-5-carboxylate to Acylation

2009

Abstract In the search for a new method of synthesis of hybrid peptides with aminopyrazole carboxylic acid, we tried to force selective acylation at the aromatic amino group instead of at the ring nitrogen atom with fairly gentle acylating agents. The acylating agents used were acid anhydrides: acetic anhydride, tert-butyl pyrocarbonate, and 2-(2-methoxyethoxy)ethoxyacetic acid/dicyclohexylcarbodiimide. We succceded in acylation at this amino group with almost none at the ring nitrogen atom. Sometimes, however, acylation in small quantities at the ring nitrogen atom was observed as a by-product. To remove this by-product, imidazole was used. Thus, we were able to obtain the hybrid peptides …

chemistry.chemical_classificationmethyl 3-amino-1H-pyrazole-5-carboxylatearomatic amineCarboxylic acidOrganic ChemistryAromatic aminePyrazoletert-butyloxycarbonylationRing (chemistry)Combinatorial chemistryAcylationchemistry.chemical_compoundAcetic anhydridechemistryacylationOrganic chemistryImidazoleCarboxylate2-(2-methoxyethoxy)ethoxyacetylationacetylationSynthetic Communications
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On the synthesis of functionalized porphyrins and porphyrin conjugates via β-aminoporphyrins

2016

International audience; The synthesis of functionalized porphyrins and their conjugates from meso-tetraarylporphyrins through the acylation and the oxidation of beta-aminoporphyrins was investigated. 2,3-Dioxochlorins were prepared by the oxidation of a variety of beta-aminoporphyrins and subsequently used in a condensation reaction with functionalized aromatic aldehydes and ammonium acetate to form beta-functionalized porphyrins bearing a fused imidazole ring. Under optimized experimental conditions both reactions tolerate various functional groups and afford the products in an appropriate overall yield. The mildness and usefulness of this methodology are illustrated by several examples in…

coordination010402 general chemistryRing (chemistry)01 natural sciences[ CHIM ] Chemical SciencesCatalysisphotoinduced electron-transferAcylationchemistry.chemical_compoundMaterials Chemistrypolycyclic compoundsImidazoleOrganic chemistry[CHIM]Chemical Sciencesalpha-dionesbuilding-blockspyrrolic position010405 organic chemistrysensitized solar-cellsbodipy dyesGeneral Chemistryefficient peripheral functionalizationCondensation reactionCombinatorial chemistryPorphyrin0104 chemical scienceswater-solubilizationchemistryYield (chemistry)systemsAmmonium acetateConjugate
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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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Acylative Dynamic Kinetic Resolution of Secondary Alcohols: Tandem Catalysis by HyperBTM and Bäckvall's Ruthenium Complex.

2021

Non-enzymatic dynamic kinetic resolution (DKR) of secondary alcohols by enantioselective acylation using an isothiourea-derived HyperBTM catalyst and racemization of slowly reacting alcohol by Backvall's ruthenium complex is reported. The DKR approach features high enantioselectivities (up to 99:1), employs easy-to-handle crystalline 4-nitrophenyl isobutyrate as the acylating reagent, and proceeds at room temperature and under an ambient atmosphere. The stereoinduction model featuring cation-π system interactions between the acylated HyperBTM catalyst and π electrons of an alcohol aryl subunit has been elaborated by DFT calculations.

inorganic chemicals010405 organic chemistryArylOrganic ChemistryEnantioselective synthesischemistry.chemical_elementStereoisomerism010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisRuthenium0104 chemical sciencesRutheniumCatalysisKinetic resolutionAcylationchemistry.chemical_compoundKineticschemistryReagentAlcoholsRacemizationThe Journal of organic chemistry
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UraniumIV and uranyle salts, efficient and reusable catalysts for acylation of aromatic compounds

2000

Abstract Uranium tetrachloride, uranyle chloride, fluoride and also nitrate or acetate are very efficient homogeneous catalysts for the Friedel–Crafts acylation of aromatic compounds. With uranyle salts, the reaction, carried under dry air, is highly specific and the mono- or bisacylation products are obtained in high yield. Uranyle catalyst can be quantitatively recovered and reused and the organic products are obtained free of uranium.

inorganic chemicalsProcess Chemistry and TechnologyHomogeneous catalysisEtherChlorideCatalysisCatalysisAcylationchemistry.chemical_compoundchemistrymedicineOrganic chemistryPhysical and Theoretical ChemistryUranium tetrachlorideFriedel–Crafts reactionFluorideNuclear chemistrymedicine.drugJournal of Molecular Catalysis A: Chemical
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Direct P-functionalization of azobenzene by a cationic phosphidozirconocene complex.

2016

International audience; We report that the cationic phosphidozirconocene complex [(eta(5)-C5H5)(2)Zr(PCy2)][CH3B(C6F5)(3)] (II) reacts with azobenzene, resulting in the expedient formation of Zr complex (2) bound to a tridentate PNN ligand. This reaction proceeds by a mechanism of cooperative nucleophilic substitution of hydrogen. The intermediate sigma(H) adduct (1) has been characterized by NMR spectroscopy.

ortho-acylationHydrogenaromatic azo-compoundschemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryBioinformatics01 natural sciences[ CHIM ] Chemical SciencesAdductalcoholsInorganic Chemistrychemistry.chemical_compoundc-h functionalizationPolymer chemistryNucleophilic substitution[CHIM]Chemical Sciences010405 organic chemistryChemistryLigandCationic polymerizationcinnolinium salts[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryNuclear magnetic resonance spectroscopy0104 chemical sciences3. Good healthAzobenzeneazoxybenzenesalpha-oxocarboxylic acidsazoareneshydrogennucleophilic-substitutionSurface modificationDalton transactions (Cambridge, England : 2003)
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A route to simple nonionic surfactants

2016

AbstractA method for the synthesis of nonionic surfactants – N-alkyl-O-(2-hydroxyethyl) carbamates is proposed by acylation of fatty amines with ethylene carbonate without any solvent or catalyst. The surface tension of the prepared surfactants was measured, toxicity and biodegradability were determined for the surfactant with n-dodecyl as a hydrophobic group and N-monosubstituted amide and hydroxyl groups for their hydrophilic part.

synthesis02 engineering and technology010402 general chemistry01 natural sciencessurfactantsCatalysisSurface tensionAcylationlcsh:Chemistrychemistry.chemical_compoundPulmonary surfactantbiodegradabilityAmidesurface tensionOrganic chemistrylcsh:ScienceEthylene carbonateGeneral EngineeringtoxicityBiodegradation021001 nanoscience & nanotechnology0104 chemical sciencesSolventchemistrylcsh:QD1-999lcsh:Q0210 nano-technologynonionic surfactantsCogent Chemistry
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