Search results for "enantiomeric excess"

showing 10 items of 37 documents

Chiral separation of bupivacaine enantiomers by capillary electrophoresis partial-filling technique with human serum albumin as chiral selector

2004

Abstract Capillary electrophoresis (CE) is a powerful technique for enantiomer separations due to its intrinsic high separation efficiencies, speed of analysis, low reagent consumption and small sample requirements. However, some chiral selectors present strong background UV absorption providing high detection limits. The present paper deals with the application of the partial-filling technique to the separation of bupivacaine enantiomers by capillary electrophoresis using human serum albumin (HSA) as chiral selector. In this procedure the cationic surfactant cetyltrimethylammonium bromide (CTAB) was used as a dinamic capillary coating in order to reduce the electro-osmotic flow and detect …

Detection limitChromatographyChemistryCapillary actionOrganic ChemistryAnalytical chemistryElectrophoresis CapillaryStereoisomerismGeneral MedicineElectrolyteHuman serum albuminBupivacaineBiochemistryAnalytical ChemistryCapillary electrophoresisPharmaceutical PreparationsReagentmedicineAnesthetics LocalEnantiomerEnantiomeric excessmedicine.drugJournal of Chromatography A
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Synthesis of 8-aminomorphans with high KOR affinity

2021

2-Azabicyclo[3.3.1]nonanes (morphans) with a (3,4-dichlorophenyl)acetyl group at 2-position and a pyrrolidino moiety at 8-position were designed as conformationally restricted analogs of piperidine-based KOR agonists. The synthesis started with 4-oxopiperidine-2-carboxylic acid comprising 13 reaction steps. At first the ketone 10 was transformed into diester 7 bearing a propionate side chain. Dieckmann condensation of diester 7 to afford bicyclic enolester 14 and subsequent Krapcho deethoxycarbonylation represent the key steps of the synthesis. The enantiomeric pyrrolidines (1S,5R,8R)-5a and (1R,5S,8S)-5a were separated by chiral HPLC. The eutomer (1S,5R,8R)-5a showed high KOR affinity (K-i…

Diastereoselective reductive aminationEnantiomeric excessStructure-affinity relationshipsPharmacologyPyrrolidinesReceptors Opioid kappaNOESY spectrumOrganic ChemistryMolecular ConformationStereoisomerismGeneral MedicineKOR agonistsEndo-configurationStructure-Activity RelationshipKOR pharmacophoreConformational restrictionChiral HPLCDihedral angleDrug DiscoveryCis/trans-configurationMorphan2-azabicyclo[3.3.1]nonaneEuropean Journal of Medicinal Chemistry
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Whole-Cell Biocatalysis in Seawater: New Halotolerant Yeast Strains for the Regio- and Stereoselectivity Reduction of 1-Phenylpropane-1,2-Dione in Sa…

2020

The application of green chemistry concepts in catalysis has considerably increased in recent years, and the interest in using sustainable solvents in the chemical industry is growing. One of the recent proposals to fall in line with this is to employ seawater as a solvent in biocatalytic processes. This involves selecting halotolerant strains capable of carrying out chemical conversions in the presence of the salt concentrations found in this solution. Recent studies by our group have revealed the interest in using strains belonging to Debaryomyces and Schwanniomyces for catalytic processes run in this medium. In the present work, we select other yeasts based on their halotolerance to wide…

Green chemistryAquatic OrganismsSalinitySaccharomyces cerevisiae010402 general chemistry01 natural sciencesBiochemistryCatalysisKluyveromycesChalconesKluyveromyces marxianusOrganic chemistryHumansSeawaterEnantiomeric excessMolecular Biologybiology010405 organic chemistryChemistryOrganic ChemistryDebaryomycesGreen Chemistry TechnologyStereoisomerismSalt Tolerancebiology.organism_classification0104 chemical sciencesSolventBiocatalysisHalotoleranceBiocatalysisMolecular MedicineFatty AlcoholsChembiochem : a European journal of chemical biology
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Determination of the Enantiomeric Purity of Levamisole and Dexamisole Using a Lanthanide Shift Reagent

1983

Utilisation de Eu(hfc) 3 (tris-[(heptafluoro hydroxy-1 butylidene-3) (+)-camphorate] europium III)

LanthanideBicyclic moleculeChemistryInorganic chemistryPharmaceutical Sciencechemistry.chemical_elementNuclear magnetic resonance spectroscopyLevamisoleReagentDrug DiscoverymedicineEnantiomerEnantiomeric excessEuropiummedicine.drugArchiv der Pharmazie
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Tertiary Chiral Nanostructures from C‐H∙∙∙F Directed Assembly of Chiroptical Superatoms

2021

Chiral hierarchical structures are universal in nature, whereas quite challenging to mimic in man-made synthesis. We report herein the synthesis and structure of tertiary chiral nanostructures with 100% optical purity. A novel synthetic strategy, using chiral reducing agent, R and S -BINAPCuBH 4 (BINAP is 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl), is developed to access to atomically precise, intrinsically chiral [Au 7 Ag 6 Cu 2 ( R - or S -BINAP) 3 (SCH 2 Ph) 6 ]SbF 6 nanoclusters in one-pot synthesis. The clusters represent the first tri-metallic superatoms with inherent chirality and fair stability. Both metal distribution (primary) and ligand arrangement (secondary) of the enantiomer…

Materials sciencevetysidoksetHydrogen bondSuperatomchiralityhierarchical nanostructuresGeneral ChemistryGeneral Medicineself-assemblyInherent chiralityCatalysisNanoclustersCrystallographychemistry.chemical_compoundkemialliset sidoksetchemistrynanorakenteetkiraalisuushydrogen bondsEnantiomercluster comboundsEnantiomeric excessChirality (chemistry)BINAP
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Natural eutectogels: sustainable catalytic systems for C–C bond formation reactions

2021

Natural eutecto gels were prepared combining properties of amino acids with the ones of deep eutectic solvents. Soft materials obtained were fully characterised determining the gel-sol transition temperatures and analysing mechanical and morphological features through rheological measurements and polarised optical microscopy. All eutecto gels were tested as catalytic reaction media for the enantioselective aldol reaction and, the best performing one was also used to carry out the Michael addition. In both cases, eutecto gels proved to have a great potential as sustainable reaction media, allowing to perform processes under mild conditions, obtaining excellent yields and, in some cases, also…

Natural eutecto gelsMaterials scienceEnantioselective synthesisC-C bond formation reactionsSettore CHIM/06 - Chimica OrganicaSustainable catalytic systemssupramolecular gels ionic liquids organocatalysiPollutionCatalysisSolventQuímica OrgánicaAldol reactionRheologyMichael reactionEnvironmental ChemistryOrganic chemistryaldol reactionEnantiomeric excessEutectic system
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Concise asymmetric synthesis of Linezolid through catalyzed Henry reaction

2013

A new asymmetric synthesis of the antibiotic Linezolid was performed through a copper-catalyzed Henry reaction as the key step. The use of camphor-derived aminopyridine ligands helped to improve the yields of the chiral precursor and to obtain Linezolid in good overall yield and enantiomeric excess.

Nitroaldol reactionChemistryorganic chemicalsGeneral Chemical EngineeringEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaGeneral Chemistrybiochemical phenomena metabolism and nutritionbacterial infections and mycosesCatalysischemistry.chemical_compoundYield (chemistry)Linezolidpolycyclic compoundsOrganic chemistryheterocyclic compoundsEnantiomeric excessasymmetric synthesis linezolid henry reaction antibioticsRSC Advances
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Conservation of optical purity of amino acids: a principal problem in biochemical and proto-biochemical systems.

1981

Dor L-amino acids, regardless of their state (peptide-bound or free, in the solid state or in aqueous solution), tend to racemize. In a living cell this racemization is usually compensated by specific degradation and replacement of the unwanted polypeptides that contain the wrong enantiomers. But a few long-lived proteins that are synthesized at or near birth are never replaced. Well investigated is the racemization of L-aspartic acid at a rate of 0.1 to 1.14 per cent per year in proteins from lenses and dentine. Increased racemization of eye lens proteins has been related to a form of human eye disease known as brunescent cataracts. Also quite well investigated is the racemization of amino…

Optical RotationStereochemistryBiologychemistry.chemical_compoundIsomerismPeptide synthesisOrganic chemistryHumansAmino AcidsEye lensEnantiomeric excessRacemizationEcology Evolution Behavior and SystematicsGeneral Environmental Sciencechemistry.chemical_classificationAspartic AcidAqueous solutionFossilsGeneral MedicineAgricultural and Biological Sciences (miscellaneous)Biological EvolutionAmino acidchemistryPolymerizationSpace and Planetary ScienceDentinGeneral Earth and Planetary SciencesEnantiomerMathematicsOrigins of life
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Synthesis of 2-isoxazolines: enantioselective and racemic methods based on conjugate additions of oximes.

2010

The formation of 3-unsubstituted 2-isoxazolines by means of condensation reactions between α,β-unsaturated aldehydes and oximes proceeds readily in the presence of catalytic amounts of anilinium salts. Mechanistically, the process involves a fast conjugate addition of the oxime and a slower intramolecular oxime-transfer reaction. The rate of oxime transfer was found to correlate with the acidity of the catalyst. This finding enabled us to discover an enantioselective process in which the fragile conjugate-addition product generated in the first stage is rapidly cyclized into the stable isoxazoline under acidic conditions, with conservation of enantiomeric excess. In summary, herein we descr…

Organic ChemistryEnantioselective synthesisGeneral ChemistryNuclear magnetic resonance spectroscopyOximeCondensation reactionCatalysisCatalysisReaction ratechemistry.chemical_compoundchemistryIntramolecular forceOrganic chemistryEnantiomeric excessChemistry (Weinheim an der Bergstrasse, Germany)
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Efficient synthesis of racemic and chiral alkenyl sulfoxides by palladium-catalyzed Suzuki coupling

2010

Alkenyl sulfoxide derivatives are obtained in high yields through a palladium-catalyzed Suzuki/Miyaura cross-coupling reaction of racemic and chiral 1-halo sulfoxides with aryl and alkenyl boronic acids. Chiral substrates react with no loss of optical purity and high optical yields. The reaction takes place with different palladium catalysts, such as Pd(PPh 3 ) 4 or Pd(OAc) 2 /DABCO. Although nitrogen ligands like DABCO lead to an active palladium catalyst, they are less effective than the phosphine ones.

Organic Chemistrychemistry.chemical_elementSulfoxideDABCOBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundchemistrySuzuki reactionDrug DiscoveryPalladium(II) acetateEnantiomeric excessPhosphinePalladiumTetrahedron
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