Search results for "SoMe"

showing 10 items of 5114 documents

Separation of homologues and isomers of linear alkylbenzenesulfonates by capillary electrophoresis with sodium dodecyl sulfate, carboxylic acids and …

2003

The ability of several anionic compounds, including carboxylic and dicarboxylic acids, sodium dodecyl sulfate (SDS), and sodium deoxycholate (SDC) and other bile salts, to separate the C(10)-C(13) homologues and the corresponding 20 positional isomers of linear alkylbenzenesulfonates (LAS) by capillary electrophoresis was studied. Up to 19 peaks and a shoulder were observed with a background electrolyte (BGE) containing 10 mM phosphate (pH 6.8), 30% acetonitrile and 40 mM SDS, and 18 peaks were obtained with a BGE containing 10 mM borate (pH 9), 40% ethanol and 40 mM palmitic acid (PA). Resolution increased with the alkyl chain length of the carboxylic acid. Dicarboxylic acids with a short …

chemistry.chemical_classificationAzelaic acidChromatographyChemistryCarboxylic acidClinical BiochemistryCarboxylic AcidsElectrophoresis CapillarySodium Dodecyl SulfateBiochemistryAnalytical ChemistryPalmitic acidBile Acids and Saltschemistry.chemical_compoundDicarboxylic acidCapillary electrophoresisIsomerismmedicineStructural isomerSodium dodecyl sulfateSulfonic AcidsAlkylmedicine.drugElectrophoresis
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Temperature and light sensitive copolymers containing azobenzene moieties prepared via a polymer analogous reaction

2009

Abstract Four different series of polyacrylamides containing different amounts of azobenzene moieties have been synthesized via a polymer analogous reaction of poly(pentafluorophenylacrylate) (PPFPA). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in aqueous solution, which was dependent on (i) the amount of incorporated chromophoric azobenzene groups and (ii) the isomerization state of the respective azobenzene group. Higher LCST values were measured for UV-irradiated solutions of the copolymers in comparison to the non-irradiated copolymer solutions. A maximum difference in the LCST of up to 7 °C was found for the copolymer poly(N,N-dimethylacrylamide…

chemistry.chemical_classificationAzo compoundPolymers and PlasticsPhotoisomerizationOrganic ChemistryPolymerLower critical solution temperatureCis trans isomerizationchemistry.chemical_compoundchemistryAzobenzenePolymer chemistryMaterials ChemistryCopolymerIsomerizationPolymer
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Peroxisomes and Hepatotoxicity

1995

Peroxisomes are ubiquitous organelles of eukaryotic cells and are present in significant amounts in hepatic liver cells. Peroxisomal enzymes contribute to several metabolic pathways including fatty acid, purine and amino acid catabolism or bile acid synthesis. The peroxisomal oxidative reactions produce hydrogen peroxide, mostly degraded by catalase which prevents oxidative stress. Moreover, peroxisomes are involved in arylderivative drug detoxification through its epoxide hydrolase activity.

chemistry.chemical_classificationCatabolismHematologyOxidative phosphorylationBiologyPeroxisomePathology and Forensic MedicineAmino acidEpoxide hydrolase activityMetabolic pathwayBiochemistrychemistryCatalaseGlyoxysomebiology.proteinAnatomyComparative Haematology International
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Alpha-(13′-hydroxy)-6-hydroxychroman, the main product of alpha-tocopherol metabolism in human hepatocytes, regulates CYP4F2 and PPAR-γ expression

2017

The enzymatic metabolism of vitamin E in liver cells generates long chain metabolites (LCMs) with proposed regulatory activity on inflammatory and atherogenic genes. In this study the LCM formation kinetics was characterized in HepG2 and HepaRG human hepatic cells, supplemented with RRR-α-tocopherol (α-TOH). α-13’OH was the main product of α-TOH metabolism, while α-13’COOH metabolite and the short chain metabolite α-CEHC, were detected only in traces, thus demonstrating the poor efficiency of vitamin E catabolism in these cells. However, this metabolism was significantly simulated when the hepatic cells were challenged with (lipo)toxic agents, such as ethanol or palmitate. Under such condit…

chemistry.chemical_classificationCatabolismMetaboliteVitamin Emedicine.medical_treatmentPeroxisome proliferator-activated receptorBiologyBiochemistrychemistry.chemical_compoundchemistryBiochemistryNuclear receptorPhysiology (medical)medicineHepatic stellate cellalpha-TocopherolDrug metabolismFree Radical Biology and Medicine
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Stereoselective Synthesis and Structural Correction of the Naturally Occurring Lactone Stagonolide G

2010

A convergent synthesis of the structure proposed for the naturally occurring lactone stagonolide G is described. All three stereocenters were created with the aid of asymmetric Brown allylations. The lactone ring was built by means of a ring-closing metathesis (RCM). The synthetic and the natural compound differed in their spectral properties. A new structure is now proposed for stagonolide G and demonstrated by means of a chemical transformation.

chemistry.chemical_classificationChemical transformationMolecular StructureChemistryStereochemistryOrganic ChemistryConvergent synthesisStereoisomerismStereoisomerismMetathesisRing (chemistry)BiochemistryCatalysisStereocenterHeterocyclic Compounds 1-RingLactonesStereoselectivityPhysical and Theoretical ChemistryLactoneOrganic Letters
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Über polystannane

1987

Abstract The three compounds Ph4Sn2(X3CCO2)2 were synthesized from Ph2SnH2 and X3CCOOH (X = H, Cl) or by cleavage of two phenyl groups in Ph6Sn2 with Stoichiometric amounts of X3CCOOH (X = Cl, F). The crystal structures (R = 0.041, 0.030, 0.058) show that the Ph4Sn2 units are bridged by two isobidentate acetates resulting in five-coordinated tin atoms. Five crystallographically independent centrosymmetric molecules form three distinct conformers. Bonding parameters (compared with Ph6Sn2): distances d(SnSn) 269, 271, 272, 277 pm; NMR couplings (CDCl3 solution) 1J(SnSn) 16870, 9443, 12915, 4480 Hz; stretching vibrations ν(SnSn) 152, 155, 157, 159 cm−. The ion pairs [Ph4Sn2]2+ [(X3CCO2)2]2−…

chemistry.chemical_classificationChemistryStereochemistryOrganic Chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyCrystal structureBiochemistryInorganic ChemistryCrystallographyX-ray crystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistryTinConformational isomerismInorganic compoundStoichiometryJournal of Organometallic Chemistry
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Regio- and stereoselective synthesis of constrained enantiomeric β-amino acid derivatives

2008

Abstract Chlorosulfonyl isocyanate addition to (−)- and (+)-apopinene furnished monoterpene-fused β-lactams in highly regio- and stereospecific reactions. β-Lactams 5 and 13 exhibited reactivities similar to those of the cycloalkane-fused analogs and were easily converted to the β-amino acid and its protected derivatives. The base-catalyzed isomerization of the cis -amino ester afforded the corresponding trans -amino acid enantiomers in excellent yields. The complete isomerization is explained by the stability difference, which was estimated by ab initio calculations between the cis- and trans -diastereomers.

chemistry.chemical_classificationChlorosulfonyl isocyanateStereochemistryOrganic ChemistryCatalysisAmino acidInorganic Chemistrychemistry.chemical_compoundStereospecificitychemistryAb initio quantum chemistry methodsStereoselectivityPhysical and Theoretical ChemistryEnantiomerIsomerizationTetrahedron: Asymmetry
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Influence of the pH on the behavior of an imprinted polymeric stationary phase--supporting evidence for a binding site model.

2001

The equilibrium isotherms of the two enantiomers of phenylalanine anilide (PA) were measured by conventional frontal analysis at three different pH on a thermally-treated imprinted stationary phase selective for the L enantiomer. The first of these pH (buffer pH=3.0, pH(app)=4.0) is well below the apparent pKa (6.4) of the two solutes, the second (buffer pH=5.8, pH(app)=7.0) slightly below this pKa, and the third (buffer pH=7.0, pH(app)=8.3) well above it. The experimental data were fitted to several isotherm models. The best estimates of the parameters of these models are reported and discussed. The corresponding isotherms are compared with the experimental ones. The contributions of the e…

chemistry.chemical_classificationChromatographyChemistryHydrogen bondPolymersCarboxylic acidPhenylalanineOrganic ChemistryBinding energyAnalytical chemistryPhenylalanineStereoisomerismStereoisomerismGeneral MedicineHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryEnantiomerMolecular imprintingJournal of chromatography. A
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Imprinted chiral stationary phases in high-performance liquid chromatography

2001

Polymers imprinted with chiral templates offer a new generation of tailor-made chiral stationary phases (CSPs) with predictable selectivities. This review summarizes the present state of the art of molecular imprinting to generate tailor-made CSPs and provides an overview of the main factors involved in the manufacturing process that are crucial to the chromatographic performance of the phases.

chemistry.chemical_classificationChromatographyManufacturing processChemistryOrganic ChemistryStereoisomerismGeneral MedicinePolymerBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryTemplatePhase compositionEnantiomerMolecular imprintingChirality (chemistry)Chromatography High Pressure LiquidJournal of Chromatography A
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Solid-state dinuclear-to-trinuclear conversion in an oxalato-bridged chromium(III)-cobalt(II) complex as a new route toward single-molecule magnets.

2011

A novel bis(oxalato)chromium(III) salt of a ferromagnetically coupled, oxalato-bridged dinuclear chromium(III)-cobalt(II) complex of formula [CrL(ox)(2)CoL'(H(2)O)(2)][CrL(ox)(2)]·4H(2)O (1) has been self-assembled in solution using different aromatic α,α'-diimines as blocking ligands, such as 2,2'-bipyridine (L = bpy) and 2,9-dimethyl-1,10-phenanthroline (L' = Me(2)phen). Thermal dehydration of 1 leads to an intriguing solid-state reaction between the S = 3/2 Cr(III) anions and the S = 3 Cr(III)Co(II) cations to give a ferromagnetically coupled, oxalato-bridged trinuclear chromium(III)-cobalt(II) complex of formula {[CrL(ox)(2)](2)CoL'} (2). Complex 2 possesses a moderately anisotropic S =…

chemistry.chemical_classificationChromiumModels MolecularOxalatesSolid-stateMolecular Conformationchemistry.chemical_elementSalt (chemistry)StereoisomerismStereoisomerismCobaltInorganic ChemistryCrystallographyBipyridinechemistry.chemical_compoundChromiumMagneticschemistryOrganometallic CompoundsMoleculePhysical and Theoretical ChemistryGround stateCobaltInorganic chemistry
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