Search results for "Selectivity"

showing 10 items of 1148 documents

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
researchProduct

Modelling retention and peak shape of small polar solutes analysed by nano-HPLC using methacrylate-based monolithic columns.

2019

Abstract The development of methacrylate-based monolithic columns was studied for the separation of pharmaceutical hydrophilic compounds in nano-liquid chromatography. The selected polymerisation mixture consisted of 7.5% hexyl methacrylate, 4.5% methacrylic acid and 18.0% ethylene dimethacrylate (w/w), in a binary porogenic solvent (35:35 w/w 1-propanol/1,4-butanediol). The polymer synthesised with this mixture has a good permeability, not excessive back-pressure, and reasonable retention times for polar and non-polar solutes. Monolithic columns (12 cm total capillary length, 100 μm i.d.), prepared with this mixture, were able to produce hydrogen bonding and electrostatic interactions, giv…

chemistry.chemical_classificationChromatography010401 analytical chemistry02 engineering and technologyPolymer021001 nanoscience & nanotechnologyMethacrylate01 natural sciencesBiochemistryHigh-performance liquid chromatography0104 chemical sciencesAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMethacrylic acidEnvironmental ChemistryAlkylbenzenesParticle size0210 nano-technologySelectivitySpectroscopyAnalytica chimica acta
researchProduct

Separation of unmodified α-amino acid enantiomers by reverse phase HPLC

1980

A novel chiral phase system is presented for the resolution of unmodified α-amino acid racemates which is composed of a reverse phase packing coated with N-alkyl-L-hydroxyproline (where alkyl is n-C7H15-, n-C10H21- and n-C16H33-) and a hydro-organic eluent containing copper(II)acetate. The factors controlling retention and enantioselectivity such as concentration of Cu(II)ion and pH of the eluent, addition of NH4Ac to the eluent, type and content of organic solvent of hydro-organic eluent and column temperature were examined. The extremely high enantioselectivity observed (α up to 16) is assumed to be caused by a three site sorbate-sorbent interaction involving bidentate coordination of two…

chemistry.chemical_classificationChromatographyChemistryOrganic ChemistryClinical BiochemistryReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryAmino acidColumn chromatographySide chainEnantiomerSelectivityAlkylChromatographia
researchProduct

Polymer-coated reversed-phase packings with controlled hydrophobic properties

1992

Abstract We have designed and synthesized novel reversed-phase packings of non-porous and porous polymethacrylate-coated silicas. By varying the hydrophobicity of the polymer coating, selective unfolding of polypeptides may be achieved, thus enabling manipulation of the chromatographic profile. This study characterizes these packings through their employment for separations of model synthetic peptides of defined secondary, tertiary and quaternary structure. Thus, the packings were applied to the reversed-phase separation α-helical amphipathic and non-amphipathic peptides of the same amino acid composition but different sequences. In addition, selective unfolding of model to-stranded α-helic…

chemistry.chemical_classificationChromatographyChemistryOrganic ChemistryGeneral MedicinePolymerBiochemistryAnalytical ChemistryAmino acid compositionPhase (matter)AmphiphilePolymer coatingProtein quaternary structureSelectivityPorosityJournal of Chromatography A
researchProduct

Application of Imprinted Synthetic Polymers in Binding Assay Development

2000

The first part of the review describes a method for the synthesis of molecularly imprinted polymers for use in binding assays. The method considers the many factors involved that affect the recognition properties of the materials and describes an approach to screening and optimization of these factors. The second part describes the development of binding assays using such polymers. This includes the use of different labels, the effect of solvent and buffer, the scale of the assay (amount of solid polymer), and how these influence the quality of the assay in terms of sensitivity, selectivity, and speed of analysis.

chemistry.chemical_classificationChromatographyChromatographyPolymersLigand binding assayDrug Evaluation PreclinicalMolecular ConformationMolecularly imprinted polymerPolymerBuffersLigandsSensitivity and SpecificityGeneral Biochemistry Genetics and Molecular BiologyPharmaceutical PreparationschemistrySolventsAdsorptionSelectivityMolecular BiologyMethods
researchProduct

Discontinuous electrokinetic chromatography of parabens using different substituted resonances as pseudostationary phases

1999

Resorcarene derivatives, negatively charged even at moderate pH, were synthesized and employed as pseudostationary phases to achieve mobilities exceeding that of the electroosmotic flow. Under these conditions, a discontinuous electrolyte system was developed which allows the separation of four uncharged homologous 4-hydroxybenzoic esters (parabens) within a zone of resorcarene electrolyte, and the detection of these UV active compounds in a resorcarene-free zone, free from the high UV background absorbance of the resorcarenes. Resorcarenes, with differently charged functionalities (carboxylate and phosphate groups) to provide the electrophoretic mobility and with alkyl residues of differen…

chemistry.chemical_classificationChromatographyClinical BiochemistryParabensElectrolyteResorcinareneBiochemistryAnalytical ChemistryAbsorbanceElectrophoresischemistry.chemical_compoundElectrokinetic phenomenachemistryCarboxylateSelectivityAlkylChromatography Micellar Electrokinetic CapillaryElectrophoresis
researchProduct

Retention behaviour of paracelsin peptides on reversed-phase silicas with varying n-alkyl chain length and ligand density.

1989

As part of further investigations on the characterization of the ligand-induced conformational stabilization of peptides, two series of n-alkyldimethylsilyl bonded silicas have been prepared. In series A the n-alkyl chain length, n, of the bonded phase was varied between 1 and 20 carbon atoms at a constant ligand density. In series B the ligand density, alpha exp, was gradually changed from 0 to 4.1 mumol/m2 on a C1, C4, C6, C8 and C18 bonded phase. The retention behaviour of four peptides of the paracelsin family were examined under isocratic conditions, using a ternary mobile phase of water-methanol-acetonitrile (22:39:39, v/v/v). Plots of k' versus n showed pronounced maxima between n = …

chemistry.chemical_classificationChromatographyLigandChemistryOrganic ChemistryMolecular Sequence DataTemperaturePeptideGeneral MedicineLigandsBiochemistryAnalytical ChemistryHydrophobic effectPartition coefficientPhase (matter)Spectrophotometry UltravioletAmino Acid SequenceTernary operationSelectivityPeptidesAlkylChromatography High Pressure LiquidAntimicrobial Cationic PeptidesJournal of chromatography
researchProduct

Development of a semiautomated procedure for the synthesis and evaluation of molecularly imprinted polymers applied to the search for functional mono…

2001

Abstract A previously described scaled-down version of the established monolith procedure, where molecularly imprinted polymers (MIPs) are prepared on the bottom surface of chromatographic vials [Anal. Chem. 71 (1999) 2092] has been here further optimised with respect to its full automation. The protocol results in savings of time and reagents compared to the monolith procedure, allowing ca. 60 polymers (∼50 mg each) to be synthesised in parallel. Both blank and imprinted polymers are then evaluated in situ by equilibrium batch rebinding tests. Each step in the synthesis and evaluation was considered with the aim of achieving an automated method with wide applicability with regards to templ…

chemistry.chemical_classificationChromatographyMolecularly imprinted polymerPolymerBiochemistryDissociation (chemistry)Analytical Chemistrychemistry.chemical_compoundMonomerTemplatechemistryPolymerizationEnvironmental ChemistryMoleculeSelectivitySpectroscopyAnalytica Chimica Acta
researchProduct

Structural selectivity provided by starburst dendrimers as pseudostationary phase in electrokinetic chromatography

1995

Abstract Starburst dendrimers (SBDs) were used as a pseudostationary phase in electrokinetic chromatography (EKC) of hydrophobic compounds. The selectivity of SBD-mediated EKC (SBD-EKC) was different from those in micellar EKC (MEKC) systems, in spite of the apparent structural resemblance between micelles and SBDs. The SBDs provided similar selectivity as polymer gel packing materials in reversed-phase liquid chromatography (RPLC), showing little selectivity for alkyl groups and clear preference for aromatic compounds, especially for rigid, planar polynuclear aromatic hydrocarbons. The alkylation of SBDs resulted in the increased retention and hydrophobic selectivity while maintaining the …

chemistry.chemical_classificationChromatographyOrganic ChemistryGeneral MedicineSBDSAlkylationBiochemistryMicelleAnalytical ChemistryElectrokinetic phenomenaHydrocarbonchemistryDendrimerOrganic chemistrySelectivityAlkylJournal of Chromatography A
researchProduct

Method for Synthesis and Screening of Large Groups of Molecularly Imprinted Polymers

2011

A technique for the synthesis of molecularly imprinted polymers (MIPs) in small scale (∼55 mg) coupled with direct in situ processing and batch rebinding evaluation is reported. The primary assessment is based on quantification by HPLC or UV absorbance measurement of the amount of template released from the polymer in a given solvent. This method allows a rapid screening of the parameters of importance to reach a desired level of binding affinity capacity and selectivity for a given target molecule. This was demonstrated for the triazine herbicide terbutylazine, where an initial screening was performed for the type of functional monomer used in the MIP preparation. Thus among the six functi…

chemistry.chemical_classificationChromatographyTrifluoromethylMolecularly imprinted polymerPolymerAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMethacrylic acidOrganic chemistryMethyl methacrylateSelectivityAcrylic acidAnalytical Chemistry
researchProduct