Search results for "Isomerism"

showing 10 items of 747 documents

Gas chromatography-fourier transform infrared spectrometry of fatty acids: New Applications with a direct deposition interface

1998

Infrared spectroscopy is a suitable spectroscopic method to differentiate geometric Z and E isomers of unsaturated compounds. A direct-deposition Fourier transform infrared spectrometer (FTIR), coupled to a gas chromatograph, was used successfully to analyze with a high sensitivity traces of C18:1 fatty acid methyl ester (FAME) isomers. It could also conclusively distinguish between isomers of conjugated diunsaturated FAME. The achievable sensitivity of this direct-deposition device makes possible accurate FAME mixture analyses that are not currently attainable with the more conventional light-pipe interface.

Chromatography010405 organic chemistryChemistryGeneral Chemical Engineering[SDV]Life Sciences [q-bio]010401 analytical chemistryOrganic ChemistryAnalytical chemistryInfrared spectroscopyTRANSFORMEE DE FOURRIERConjugated system01 natural sciences0104 chemical sciences[SDV] Life Sciences [q-bio]chemistry.chemical_compoundsymbols.namesakeFourier transformsymbolsGas chromatographyFourier transform infrared spectroscopyCis–trans isomerismUnsaturated fatty acidFatty acid methyl esterComputingMilieux_MISCELLANEOUS
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Chiral determination of amphetamine and related compounds using chloroformates for derivatization and high-performance liquid chromatography

1999

The enantiomeric determination of amphetamine and various amphetamine-type compounds by liquid chromatography after chiral derivatization with 9-fluorenylmethyl chloroformate-L-proline (FMOC-L-Pro) is reported. The results obtained were compared with those achieved after achiral derivatization with 9-fluorenylmethyl chloroformate and subsequent separation of the derivatives on a beta-cyclodextrin chiral stationary phase. Conditions for the derivatization of amphetamines with FMOC-L-Pro were investigated, including the effect of the derivatization reagent concentration, pH and reaction time, using amphetamine, ephedrine and pseudoephedrine as model compounds. On the basis of these studies, p…

ChromatographyAmphetaminesStereoisomerismChloroformatePseudoephedrineSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryReagentElectrochemistrymedicineEnvironmental ChemistryOrganic chemistryCentral Nervous System StimulantsEnantiomerEphedrineDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidSpectroscopymedicine.drugThe Analyst
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Homochiral Metal-Organic Frameworks for Enantioselective Separations in Liquid Chromatography

2020

Selective separation of enantiomers is a substantial challenge for the pharmaceutical industry. Chromatography on chiral stationary phases is the standard method, but at a very high cost for industrial-scale purification due to the high cost of the chiral stationary phases. Typically, these materials are poorly robust, expensive to manufacture, and often too specific for a single desired substrate, lacking desirable versatility across different chiral analytes. Here, we disclose a porous, robust homochiral metal–organic framework (MOF), TAMOF-1, built from copper(II) and an affordable linker prepared from natural l-histidine. TAMOF-1 has shown to be able to separate a variety of model…

ChromatographyMolecular StructureChemistryIndustrial scaleEnantioselective synthesisQuímica organometàl·licaWaterStereoisomerismStereoisomerismGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryHigh-performance liquid chromatography54Catalysis0104 chemical sciencesColloid and Surface ChemistryMoleculeWater chemistryMetal-organic frameworkEnantiomerChromatography High Pressure LiquidCopperMetal-Organic Frameworks
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In-line capillary electrophoretic evaluation of the enantioselective metabolism of verapamil by cytochrome P3A4

2013

Abstract In this paper a methodology for the in-line evaluation of enantioselective metabolism by capillary electrophoresis has been developed and applied to the study of verapamil metabolism by cytochrome P3A4. The developed methodology comprises an in-capillary reaction step carried out by electrophoretically mediated microanalysis and a separation step in which highly sulfated β-cyclodextrin with partial filling technique has been employed as chiral selector for verapamil and norverapamil enantiomers resolution, joining the advantages of both methodologies in a unique assay. Kinetic parameters of the enzymatic reaction (Km and Vmax) have been evaluated for both verapamil enantiomers by n…

ChromatographyMolecular StructureCytochromebiologyReaction stepChemistryOrganic ChemistryEnantioselective synthesisElectrophoresis CapillaryStereoisomerismNorverapamilGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundElectrophoresisCapillary electrophoresisVerapamilmedicinebiology.proteinVerapamilEnantiomerSoftwaremedicine.drugJournal of Chromatography A
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Ferromagnetic coupling and magnetic anisotropy in oxalato-bridged trinuclear chromium(iii)-cobalt(ii) complexes with aromatic diimine ligands

2010

Two novel heterotrinuclear chromium(III)-cobalt(II) complexes of formula {[Cr(III)(bpy)(ox)(2)](2)Co(II)(Me(2)bpy)}.2H(2)O (1) and {[Cr(III)(phen)(ox)(2)](2)Co(II)(Me(2)bpy)}.1.5H(2)O (2) [ox = oxalato, bpy = 2,2'-bipyridine, Me(2)bpy = 6,6'-dimethyl-2,2'-bipyridine, and phen = 1,10-phenanthroline] have been synthesized using the "complex-as-ligand/complex-as-metal" strategy. The X-ray crystal structure of 2 consists of neutral oxalato-bridged Cr(III)(2)Co(II) bent entities formed by the coordination of two anionic [Cr(III)(phen)(ox)(2)](-) complexes through one of their oxalato groups toward a cationic cis-[Co(II)(Me(2)bpy)](2+) complex. The three tris(chelated), six-coordinated metal atom…

ChromiumModels MolecularOxalatesMolecular StructureChemistryStereochemistrySupramolecular chemistryStereoisomerismCobaltCrystal structureCrystallography X-RayLigandsMagnetic susceptibilityInorganic ChemistryMagneticsCrystallographyMagnetic anisotropyIntramolecular forceOrganometallic CompoundsAnisotropyAntiferromagnetismMolecular orbitalIminesDiimineDalton Trans.
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Synthesis and mutagenicity of the diastereomeric fjord-region 11,12-dihydrodiol 13,14-epoxides of dibenzo[a,l]pyrene.

1994

Extensive tumorigenicity studies in rodents revealed that dibenzo[a,l]pyrene (DB[a,l]P) is the most potent carcinogen among all polycyclic aromatic hydrocarbons (PAHs) tested so far. The structure of the genotoxic metabolite(s) responsible for this exceptional carcinogenicity is unknown. The fjord-region syn- and anti-DB[a,l]P-11,12-dihydrodiol 13,14-epoxides (syn- and anti-DB[a,l]PDE) were synthesized to clarify their role as possible ultimate mutagenic and carcinogenic metabolites of DB[a,l]P.9-Formyl-11,12-dimethoxybenzo[g] chrysene was prepared from 9-phenanthrylacetic acid by a photochemical route. After reaction of the aldehyde with trimethylsulfonium iodide to generate an oxiranyl si…

ChryseneSalmonella typhimuriumCancer ResearchStereochemistryMetaboliteMutagenStereoisomerismmedicine.disease_causeChemical synthesisAmes testDihydroxydihydrobenzopyreneschemistry.chemical_compoundCricetulusCricetinaemedicineAnimalsheterocyclic compoundsBenzopyrenesCarcinogenCells CulturedStereoisomerismGeneral MedicineBiochemistrychemistryCarcinogensPyreneEpoxy CompoundsMutagensCarcinogenesis
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Relationship between mutagenicity and DNA adduct formation in mammalian cells for fjord- and bay-region diol-epoxides of polycyclic aromatic hydrocar…

1991

Abstract Chinese hamster V79 cells were treated with the anti- and syn-diastereomers of the bay- or fjord-region diol-epoxides of four polycyclic aromatic hydrocarbons, namely benzo[a]pyrene (BP), benzo[c]chrysene (BcC), benzo[g]chrysene (BgC) and benzo[c]phenanthrene (BcPh). The frequency of induction of 6-thioguanine-resistant mutations was determined, and the extent of formation of DNA adducts was measured by 32P-postlabelling. When expressed as mutation frequency per nanomoles compound per millilitre incubation medium, this group of chemicals expressed a 160-fold range in potency. In agreement with previous experimental studies, the anti-diol-epoxide of BcC was highly mutagenic, inducin…

ChryseneStereochemistryCell SurvivalBenzo(c)phenanthreneToxicologyAdductchemistry.chemical_compoundCricetulusIsomerismCricetinaepolycyclic compoundsBenzo(a)pyreneAnimalsheterocyclic compoundsPolycyclic CompoundsMutation frequencyCells Culturedintegumentary systemorganic chemicalsfungiGeneral MedicineDNAPhenanthrenechemistryBenzo(a)pyreneMutationPyreneDNAMutagensChemico-biological interactions
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DNA adduct levels associated with p53 induction and delay of MCF-7 cells in S phase after exposure to benzo[g]chrysene dihydrodiol epoxide enantiomer…

1998

Optically active isomers of a mammary carcinogen, anti-benzo[g]chrysene 11, 12-dihydrodiol 13, 14-epoxide, react to different extents with DNA and generate DNA adducts that differ in their stereochemistry. In the study reported here, the effect of these two enantiomers on the progress of human breast carcinoma MCF-7 cells through the cell cycle was investigated. Each enantiomer caused the cells to accumulate in the S phase, but a higher dose of the benzo[g]chrysene 11S, 12R-dihydrodiol 13R, 14S-epoxide than of its enantiomer was required to induce this effect. Similarly, induction of p53 also required a higher dose of benzo[g]chrysene 11S, 12R-dihydrodiol 13R, 14S-epoxide. Postlabeling stud…

Chrysenechemistry.chemical_classificationCancer ResearchStereochemistryStereoisomerismBiologyCell cycleChrysenesAdductS Phasechemistry.chemical_compoundDNA AdductschemistryDNA adductpolycyclic compoundsTumor Cells CulturedHumansNucleotideEnantiomerTumor Suppressor Protein p53Molecular BiologyCarcinogenDNAMolecular carcinogenesis
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Pauson-Khand reaction of internal dissymmetric trifluoromethyl alkynes. Influence of the alkene on the regioselectivity.

2014

Abstract: The scope of the Pauson-Khand reaction (PKR) of internal trifluoromethyl alkynes, previously described with norbornadiene, is expanded to norbornene and ethylene. A thorough structural analysis of the resulting PK adducts has been carried out to unveil that α-trifluoromethylcyclopentenones are preferred in all cases, independently of the electronic properties of the alkyne. The regioselectivity observed with norbornadiene and ethylene is higher than in the case of norbornene.

Ciclització (Química)EthyleneHydrocarbons FluorinatedStereochemistryNorbornadieneQuímica organometàl·licaPharmaceutical ScienceAlkynetrifluoromethylalkynesCrystallography X-RayArticlecyclopentenonesAnalytical ChemistryRing formation (Chemistry)cycloadditionslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryPhysical and Theoretical ChemistryNorbornenechemistry.chemical_classificationPauson-Khand reactionTrifluoromethylMolecular StructureAlkenePauson–Khand reactionOrganic ChemistryRegioselectivityStereoisomerismCobaltEthylenesNorbornaneschemistryOrganometallic chemistryChemistry (miscellaneous)AlkynesregioselectivityMolecular MedicineMolecules (Basel, Switzerland)
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Enantiomeric separation of chiral phenoxy acid herbicides by electrokinetic chromatography. Application to the determination of analyte-selector appa…

2001

The enantiomeric resolution of chiral phenoxy acid herbicides was performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC). A systematic evaluation of several neutral and charged cyclodextrins was made. Among the cyclodextrins tested, (2-hydroxy)propyl beta-cyclodextrin (HP-beta-CD) was found to be the most appropriate for the enantioseparation of phenoxy acids. The influence of some experimental conditions, such as nature and pH of the background electrolyte, chiral selector concentration, and temperature, on the enantiomeric separation of phenoxy acids was also studied. The use of a 50 mM electrolyte solution in ammonium formate at pH 5 and a temperat…

CienciaAnalyteElectrokinetic chromatographyResolution (mass spectrometry)ScienceChemistry analytic and technicalClinical BiochemistryElectrolytePhenoxy acid herbicidesBiochemistryAnalytical ChemistryElectrolyteschemistry.chemical_compoundElectrokinetic phenomenaTwo temperatureCIENCIAAmmonium formateOrganic chemistrychemistry.chemical_classificationChromatographyCyclodextrinsChromatographyCyclodextrinHerbicidesChemistryPhenyl Ethersbeta-CyclodextrinsTemperatureStereoisomerismQuímica analítica e industrialSCIENCEHydrogen-Ion Concentration2-Hydroxypropyl-beta-cyclodextrinSolutionsPropionatesEnantiomerELECTROPHORESIS
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