Search results for "Tetra"

showing 10 items of 6481 documents

Mono- and Bidentate Phosphine Ligands in the Palladium-Catalyzed Methyl Acrylate Dimerization

2003

The influence of several phosphine ligands on the activity, selectivity and stability of the catalytic system Pd(acac)2, ligand, [HOEt2][BF4] was studied in the dimerization of methyl acrylate (MA). It was found that the catalyst's activity increased with increasing the basicity of the monodentate ligands used, whereas bulky phosphines lowered the linearity of the dimers and the reaction rates. With chelating P N-, P P-, and P As-ligands the Pd-catalyst could be efficiently stabilized during the reaction. The use of 1-dibutylphosphino-2-dimethylaminoethane as ammonium tetrafluoroborate salt allowed the highest overall activity.

DenticityTetrafluoroborateLigandchemistry.chemical_elementGeneral ChemistryMedicinal chemistryCatalysischemistry.chemical_compoundchemistryOrganic chemistryChelationMethyl acrylatePhosphinePalladiumAdvanced Synthesis & Catalysis
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X-ray crystal structure and antimony-121 Mössbauer spectrum of catecholato bis(1,10-phenanthroline)antimony(III) tetraphenylborate

1985

The crystal structure of the title compound was solved by means of X-ray diffraction at room temperature. The salt consists of a tetrahedral tetraphenylborate anion and a complex cation containing a catecholatoantimony(III) unit chelated by two 1,10-phenanthrolines. The three bidentate ligands are essentially arranged in one half of the Sb coordination sphere, leaving ample space to accomodate the lone pair of electrons. The Mossbauer parameters of the title compound and of the complex (C6H4O2)SbF·Phen were measured and their rationalization accomplished in the light of their respective molecular structures.

DenticityTetraphenylborateCoordination spherePhenanthrolineInorganic chemistrychemistry.chemical_elementCrystal structureInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAntimonyX-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistryLone pairInorganica Chimica Acta
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Organometallic complexes with biological molecules. IX. Diorgano- and triorgano-tin(IV)[meso-tetra (4-sulfonatophenyl)porphinate] derivatives: solid-…

1997

Diorgano- and triorgano-tin(IV) derivatives of meso-tetra(4-sulfonatophenyl)porphine (H4TPPS) with general formula (R2Sn)2TPPS and (R3Sn)4TPPS (TPPS4−=[meso-tetra(4-sulfonatophenyl)porphinate]4−, R=Me, Bu, Ph) have been obtained and their solid-state configuration inferred on the basis of IR and Mossbauer spectroscopy, while solution-phase studies have been carried out by 1H and 13C NMR in DMSO-d6, together with determination of the in vivo cytotoxicity of the new derivatives towards embryonic development of Ciona intestinalis. In particular, octahedral and trigonal-bipyramidal eq-R3Sn polymeric configurations are proposed, in the solid state, respectively for (R2Sn)2TPPS and (R3Sn)4TPPS co…

DenticitybiologyChemistryMeso compoundStereochemistryInfrared spectroscopyGeneral ChemistryCarbon-13 NMRbiology.organism_classificationChemical synthesisInorganic ChemistryCrystallographyOctahedronMössbauer spectroscopyTetraApplied Organometallic Chemistry
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Inhibition of pro-inflammatory enzymes by inuviscolide, a sesquiterpene lactone from Inula viscosa

2006

Abstract This work concerns the pharmacological activity of inuviscolide, a sesquiterpenoid from Inula viscosa. It exerts inhibitory effects on elastase, cyclooxygenase 1 and secretory phospholipase A2. Furthermore, it reduces the skin leukocyte infiltration in a murine model of dermatitis induced by repeated application of 12-O-tetradecanoylphorbol 13-acetate.

DermatitisBiologyPharmacognosyPharmacologySesquiterpene lactoneSesquiterpeneLactonesMicechemistry.chemical_compoundDrug DiscoveryLeukocytesAnimalsHumansEnzyme InhibitorsPharmacologychemistry.chemical_classificationPancreatic Elastaseintegumentary systemPlant ExtractsAnti-Inflammatory Agents Non-SteroidalElastaseBiological activityGeneral MedicineEnzymechemistryBiochemistrybiology.proteinTetradecanoylphorbol AcetateInulaCyclooxygenaseSesquiterpenesLactonePhytotherapyFitoterapia
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Simultaneous quantification of 18 different phytocannabinoids in serum using a highly sensitive liquid chromatography-tandem mass spectrometry (LC-MS…

2021

Abstract The potential therapeutic effects of various phytocannabinoids and the availability of multiple cannabis-based medicines make it desirable to have an analytical method that simultaneously quantifies a wide range of cannabinoids in blood, beyond delta-9-tetrahydrocannabinol and its metabolites. A liquid chromatography tandem mass spectrometry (LC-MS/MS) method for quantification of 18 phytocannabinoids and cannabinoid metabolites in serum was developed and validated. The method enables simultaneous detection of delta-9-tetrahydrocannabinol, cannabidiol, cannabinol, cannabigerol, cannabichromene, cannabicyclol, tetrahydrocannabivarin and cannabidivarin and their acidic precursors tet…

Detection limitChromatographyCannabigerol010401 analytical chemistryClinical BiochemistryCell BiologyGeneral MedicineTetrahydrocannabivarin030226 pharmacology & pharmacy01 natural sciencesBiochemistryCannabicyclol0104 chemical sciencesAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundCannabichromene0302 clinical medicinechemistryLiquid chromatography–mass spectrometrymedicineCannabinolSolid phase extractionmedicine.drugJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Effect of the shampoo Ultra Clean on drug concentrations in human hair

2000

The influence of the special shampoo Ultra Clean (Zydot Unlimited, Tulsa, Oklahoma) on the results of hair analyses was investigated. Hair samples from persons (n = 14) with a known history of drug abuse were collected at autopsy. The hair samples were divided into separate strands which were analyzed both after washing with Ultra Clean and without treatment. Hair analyses were performed by methanol extraction under sonication, purification by solid phase extraction and GC/MS in SIM mode according to routine procedures for tetrahydrocannabinol (THC), cocaine, amphetamine, methylenedioxyamphetamine (MDA), methylenedioxymethamphetamine (MDMA), methylenedioxyethylamphetamine (MDE), heroin, 6-m…

Detection limitChromatographyChemistryCodeineHair PreparationsMDMAForensic MedicineDihydrocodeineShampooPathology and Forensic MedicineSubstance Abuse DetectionmedicineMorphineHumansSolid phase extractionTetrahydrocannabinolHairmedicine.drugInternational Journal of Legal Medicine
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RAPID LIQUID CHROMATOGRAPHIC DETERMINATION OF TETRACYCLINES IN ANIMAL FEEDS USING A SURFACTANT SOLUTION AS MOBILE PHASE

2002

ABSTRACT A chromatographic procedure was developed for the determination of oxytetracycline (OTC), tetracycline (TC), chlortetracycline (CTC), doxycycline (DC) and minocycline (MINO) in animal feeds. Clear analyte-rich extracts were obtained using a 1 : 1 acetonitrile/water mixture buffered at pH 3. The extracts were injected into a conventional unprotected C18 chromatographic column and eluted with a mobile phase of 0.05 M sodium dodecyl sulfate/5% 1-butanol/0.01 M oxalic acid at pH 3. Good resolution was achieved for the five compounds, whereas OTC and TC coeluted with an optimized aqueous-organic mobile phase of methanol/acetonitrile/0.01 M oxalic acid at pH 3. Mean recoveries from spike…

Detection limitChromatographyChemistryElutionBiochemistry (medical)Clinical BiochemistryOxalic acidOxytetracyclineBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographyElectrochemistrymedicineSodium dodecyl sulfateSpectroscopymedicine.drugAntibacterial agentAnalytical Letters
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MICELLAR LIQUID CHROMATOGRAPHIC DETERMINATION OF ANTI-CONVULSANT DRUGS IN PILLS AND CAPSULES

2000

A simple chromatographic procedure is reported for the determination of several anti-convulsant drugs in pharmaceuticals: carbamazepine, and the benzodiazepines bentazepam, halazepam, oxazepam, pinazepam, and tetrazepam. The procedure utilizes a C18 column, a hybrid micellar mobile phase of 0.1 M SDS-3% butanol-0.1% triethylamine-0.01 M phosphate buffer (pH 3), and UV detection (230 nm). The drugs eluted in less than 13 min, in accordance to their relative polarities, as indicated by their octanol-water partition coefficients. The limits of detection (μg/mL), and intra and inter-day repeatabilities (%), for 4 μg/mL were: carbamazepine (0.03, 1.0, 4.1), bentazepam (0.05, 1.3, 1.6), halazepam…

Detection limitChromatographyPinazepamChemistryClinical BiochemistryPharmaceutical ScienceBiochemistryBentazepamHalazepamDosage formMicellar electrokinetic chromatographyAnalytical ChemistryOxazepamTetrazepammedicinemedicine.drugJournal of Liquid Chromatography & Related Technologies
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Matrix solid-phase dispersion extraction procedure for multiresidue pesticide analysis in oranges.

1996

A multiresidue extraction method based on matrix solid-phase dispersion (MSPD) is optimized for the extraction and gas chromatographic screening of eighteen insecticides (aldrin, carbophenothion, captafol, chlorpyriphos, chlorfenvinphos, diazinon, dicofol, alpha-endosulfan, beta-endosulfan, ethion, fenitrothion, folpet, methidathion, malathion, methyl-azinphos, methyl-parathion, phosmet, and tetradifon) from oranges. After optimization of different parameters, such as type of solid phase used and the amount of solid phase or eluent, recoveries ranged from 67 to 102% with relative standard deviations ranging from 2 to 10%. The limits of detection, calculated as 3 times the baseline noise ran…

Detection limitCitrusChromatographyChromatography GasPesticide residueMicrochemistryOrganic ChemistryAnalytical chemistryPesticide ResiduesGeneral MedicinePhosmetMethidathionAcetatesEthionBiochemistrySensitivity and SpecificityAnalytical ChemistryTetradifonchemistry.chemical_compoundchemistryCarbophenothionSolventsAldrinJournal of chromatography. A
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ChemInform Abstract: Diels-Alder Reactions of in situ Generated N-Benzoylindolo-2,3- quinodimethane with Carbodienophiles.

2010

The indolo-2,3-quinodimethane (5), generated from 2,3-bis(bromomethyl)indole (4), was trapped with unsymmetrical carbodienophiles or N, N′-p-phenylenedimaleimide to furnish the 1,2,3,4-tetrahydrocarbazoles (6–9). [4 + 2]-Cycloaddition of 5 with tetracyanoethylene gave rise to the tetracyanocarbazole (10) and a subsequent product 11a or 11b. The Diels-Alder reaction of 5 with divinyl sulfone was regiospecific within the detection limits of HPLC analysis. Similarly, the reaction of 5 with N, N′-p-phenylenedimaleimide yielded solely the stereoisomer 9.

Detection limitIndole testIn situHplc analysischemistry.chemical_compoundchemistryDiels alderGeneral MedicineTetracyanoethyleneMedicinal chemistryDivinyl sulfoneChemInform
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