Search results for "Reagent"

showing 10 items of 699 documents

Screening of oxazepine indole enantiomers by means of high performance liquid chromatography with imprinted polymer stationary phase.

2004

Chromatographic enantiomer separations of different oxazepine indole derivatives were performed using a molecularly imprinted polymer. A 5aR,12R,13S-trans-6,6-dimethyl-12,13-dihydro-6H-5a, 1 3-methanoindolo[2,1-b][1,3]naphthoxazepine-12-carboxamide enantiomerderivative was used as a template and the resultant polymer has shown enantiomer recognition for series of template related compounds. The mechanistic description of the chiral discrimination process is scrutinised, comparing the discrimination between the different conformations and substituents of the oxazepine indoles.

Indole testchemistry.chemical_classificationModels MolecularMolecularly imprinted polymerFiltration and SeparationStereoisomerismPolymerHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundOxazepineschemistryStationary phaseOrganic chemistryOxazepineIndicators and ReagentsEnantiomerMolecular imprintingChromatography High Pressure LiquidJournal of separation science
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Chemical profiling of the synthetic cannabinoid MDMB-CHMICA: Identification, assessment, and stability study of synthesis-related impurities in seize…

2019

In this work, the most discriminating synthesis-related impurities found in samples from seizures and controlled synthesis of the synthetic cannabinoid MDMB-CHMICA (methyl (S)-2-(1-(cyclohexylmethyl)-1H-indole-3-carboxamido)-3,3-dimethylbutanoate) were characterized. Based on 61 available powder samples of MDMB-CHMICA, 15 key-impurities were assessed, isolated in larger quantities via flash chromatography and structurally elucidated and characterized via high resolution mass spectrometry and nuclear magnetic resonance spectroscopy. Apart from verifying the relation of the impurities to the major component, the interpretation of their chemical structures with distinct structural elements pro…

IndolesControlled Synthesis ; Impurity Profiling ; Lc-ms ; Mdmb-chmica ; New Psychoactive Substances (nps)Pharmaceutical Science01 natural sciencesAnalytical Chemistry03 medical and health scienceschemistry.chemical_compound0302 clinical medicineColumn chromatographyThionyl chlorideOxalyl chlorideDrug StabilityLiquid chromatography–mass spectrometryImpurityTandem Mass SpectrometryEnvironmental ChemistryHATU030216 legal & forensic medicineDrug TraffickingSpectroscopyChromatography High Pressure LiquidChromatographyChemistryCannabinoidsIllicit Drugs010401 analytical chemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesReagentDrug Contamination
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Sequential injection analysis (SIA)-chemiluminescence determination of indomethacin using tris[(2,2'-bipyridyl)]ruthenium(III) as reagent and its app…

2006

Abstract Automated sequential injection (SIA) method for chemiluminescence (CL) determination of nonsteroidal anti-inflammatory drug indomethacin ( I ) was devised. The CL radiation was emitted in the reaction of I (dissolved in aqueous 50% v/v ethanol) with intermediate reagent tris(2,2′-bipyridyl)ruthenium(III) (Ru(bipy) 3 3+ ) in the presence of acetate. The Ru(bipy) 3 3+ was generated on-line in the SIA system by the oxidation of 0.5 mM tris(2,2′-bipyridyl)ruthenium(II) (Ru(bipy) 3 2+ ) with Ce(IV) ammonium sulphate in diluted sulphuric acid. The optimum sequence, concentrations, and aspirated volumes of reactant zones were: 15 mM Ce(IV) in 50 mM sulphuric acid 41 μL, 0.5 mM Ru(bipy) 3 …

IndomethacinAnalytical chemistrychemistry.chemical_elementBiochemistryDosage formAnalytical Chemistrylaw.inventionlawSpectrophotometrymedicineOrganometallic CompoundsEnvironmental ChemistrySpectroscopyChemiluminescenceDetection limitDosage FormsAqueous solutionmedicine.diagnostic_testMolecular StructureReproducibility of ResultsRutheniumStandard curvechemistryReagentCalibrationFlow Injection AnalysisLuminescent MeasurementsSolventsNuclear chemistryAnalytica chimica acta
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Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA.

2004

Primary defence against invading microorganisms depends on a functional innate immune system and the complement system plays a major role in such immunity. Deficiencies in one of the components of the complement system can cause severe and recurrent infections, systemic diseases, such as systemic lupus erythematosus (SLE) and renal disease. Screening for complement deficiencies in the classical or alternative complement pathways has mainly been performed by haemolytic assays. Here, we describe a simple ELISA-based format for the evaluation of three pathways of complement activation. The assays are based on specific coatings for each pathway in combination with specific buffer systems. We ha…

Innate immune systemSystemic lupus erythematosusImmunologyComplement Pathway AlternativeComplement Pathway Mannose-Binding LectinEnzyme-Linked Immunosorbent AssayComplement System ProteinsBiologyComplement fixation testmedicine.diseaseMannose-Binding LectinComplement systemComplement (complexity)Immune systemImmunologymedicineImmunology and AllergyHumansLupus Erythematosus SystemicComplement Pathway ClassicalReagent Kits DiagnosticFicolinComplement ActivationMannan-binding lectinJournal of immunological methods
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Cyclization of the pyruvyl(methoxycarbonyl)tetracarbonyliron complex cis-(CO)4Fe[C(O)C(O)CH3](CO2CH3) induced by pronucleophile reagents

2002

International audience; Two iron complexes, cis-(CO)4Fe[C(O)C(O)CH3](CO2CH3) (1a) and cis-(CO)4Fe[C(O)CO2-CH2] [C(O)CH2] (3), are reported. Each complex can be considered as a λ-keto ester with a metal atom inserted into the chain linking its two organic groups. 1a is the only one found to evolve thermally, similarly to organic λ-keto esters, into the methoxy metallalactone (CO)4FeC(O)C(CH3)(OCH3)OC(O) (2a). This reaction is not reversible and does not require any acid or alkaline catalysis. The process does not result from a spontaneous dissociation of the methoxycarbonyl ligand of la but from an associative intra or intermolecular mechanism. A similar process can also be induced by pronuc…

Inorganic Chemistry010405 organic chemistryStereochemistryChemistryReagentOrganic ChemistryAtom (order theory)[CHIM]Chemical SciencesPhysical and Theoretical Chemistry010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciences
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Zirconocene complexes bearing novel 3-dimethylamino-1,2-dihydropentalene derived ligand systems.

2010

Coupling of the N,N-dimethylacrylamides 6a-c with cyclopentadienide resulted in the formation of the substituted 3-dimethylamino-1,2-dihydropentalnenes 2a-c. Deprotonation followed by metallation with CpZrCl(3)·DME gave the substituted zirconocenes 12a-c. The reaction of 3-dimethylamino-1-methyl-dihydropentalene 2a with ZrCl(2)(NMe(2))(2)·2THF resulted in a unique coupling between a pair of the aminodihydropentalene derivatives to yield an unsymmetrically bridged novel ansa-zirconocene framework (9a). Treatment of the 1,1-dimethyl-substituted substrate 2b with this Zr-amido reagent in contrast resulted in a clean deprotonation and formation of the unbridged bis(dimethylaminohydropentalenyl)…

Inorganic ChemistryDeprotonationChemistryLigandStereochemistryReagentYield (chemistry)Substrate (chemistry)Medicinal chemistryDalton transactions (Cambridge, England : 2003)
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A convenient synthetic route to useful monobranched polyethoxylated halogen terminated [3,3 -Co(1,2-C2B9H11)2]- synthons

2009

An atom efficient and environmentally friendly route has been developed to obtain a new range of reagents in metallacarborane chemistry having monobranched polyethoxylated cobaltabisdicarbollide synthons. peer-reviewed

Inorganic ChemistryMonobranched polyethoxylated halogenChemistryChemistryReagentHalogenHalogenSynthonOrganic chemistryEnvironmentally friendlyCombinatorial chemistry
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Reactions of (η5-C5H5)(CO)2Fe-Substituted N-Sulfonyl Azadienes with C-Nucleophiles. A Route to 5-Substituted Dihydropyrrolones

2000

A variety of cyclic β-[(η5-C5H5)(CO)2Fe]-substituted N-sulfonyl azadienes 4 were prepared:  e.g., from the corresponding iron-substituted (Z)-enals and benzenesulfonamide. Reactions of these iron compounds with Grignard reagents or organolithiums gave 5-substituted α,β-unsaturated N-sulfonyl γ-lactams 5. In some cases the corresponding non-N-protected 5-substituted γ-lactams 6 were isolated as well. Key steps of these reaction cascades are the initial 1,2-addition to the imine moiety and the subsequent carbonylation step. The reaction of the chromene−iron complex 4e with (allyl)MgCl gave the (η3-allyl)iron−γ-lactam complex 8a with a ring-opened chromene framework. This complex was structura…

Inorganic ChemistrySulfonylchemistry.chemical_classificationchemistry.chemical_compoundNucleophilechemistryReagentOrganic ChemistryImineMoietyPhysical and Theoretical ChemistryMedicinal chemistryCarbonylationOrganometallics
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A Nonconventional Approach toward Multihydroxy Functional Polystyrenes Relying on a Simple Grignard Reagent

2020

Capitalizing on the inertness of styrene toward Grignard reagents, 4-vinylphenylmagnesium bromide was utilized for the rapid and convenient preparation of the protected monomer 2,2-dimethyl-4-(4-vi...

Inorganic Chemistrychemistry.chemical_compoundMonomerPolymers and PlasticschemistryBromideSimple (abstract algebra)ReagentOrganic ChemistryMaterials ChemistryGrignard reagentCombinatorial chemistryStyreneMacromolecules
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Highly diastereoselective additions of organometallic reagents to 1-O-silylated 3,4-Di-O-benzyl-L-erythrulose derivatives

1993

Abstract The diastereoselectivity of the addition of several organometallic reagents to the carbonyl group of the title compounds has been investigated. Some organomagnesium reagents display high diastereoselectivities (90–99%) and the major products are those predicted by the α-chelation model.

Inorganic Chemistrychemistry.chemical_compoundNucleophilic additionchemistryReagentOrganic ChemistryOrganic chemistryChelationPhysical and Theoretical ChemistryL-ERYTHRULOSECarbonyl groupCatalysisTetrahedron: Asymmetry
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