Search results for "TRIF"

showing 10 items of 1419 documents

In Situ Ammonium Profiling Using Solid-Contact Ion-Selective Electrodes in Eutrophic Lakes

2015

A promising profiling setup for in situ measurements in lakes with potentiometric solid-contact ion-selective electrodes (SC-ISEs) and a data processing method for sensor calibration and drift correction are presented. The profiling setup consists of a logging system, which is equipped with a syringe sampler and sensors for the measurement of standard parameters including temperature, conductivity, oxygen and photosynthetically active radiation (PAR). The setup was expanded with SC-ISEs in galvanically separated amplifiers. The potential for high-resolution profiling is investigated by deploying the setup in the eutrophic Lake Rotsee (Lucerne, Switzerland), using two different designs of am…

In situAnalyteBiogeochemical cycleDenitrificationChemistryPotentiometric titrationAnalytical chemistrySulfidesConductivity6. Clean waterAnalytical ChemistryLakeschemistry.chemical_compoundEnvironmental chemistryAmmonium Compoundsddc:540AmmoniumNitrogen cycleIon-Selective ElectrodesEnvironmental MonitoringANALYTICAL CHEMISTRY
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Predicting in situ soil N2O emission using NOE algorithm and soil database

2005

This paper presents a new algorithm, Nitrous Oxide Emission (NOE) for simulating the emission of the greenhouse gas N2O from agricultural soils. N2O fluxes are calculated as the result of production through denitrification and nitrification and reduction through the last step of denitrification. Actual denitrification and nitrification rates are calculated from biological parameters and soil water-filled pore space, temperature and mineral nitrogen contents. New suggestions in NOE consisted in introducing (1) biological site-specific parameters of soil N2O reduction and (2) reduction of the N2O produced through nitrification to N2 through denitrification. This paper includes a database of 6…

In situDenitrification010504 meteorology & atmospheric sciences[SDE.MCG]Environmental Sciences/Global ChangesSoil science01 natural scienceschemistry.chemical_compoundSoil databaseEnvironmental ChemistryComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesGeneral Environmental ScienceGlobal and Planetary ChangeEcology04 agricultural and veterinary sciencesNitrous oxideMineral nitrogen[SDE.MCG] Environmental Sciences/Global Changeschemistry13. Climate actionGreenhouse gasSoil water040103 agronomy & agriculture0401 agriculture forestry and fisheriesEnvironmental scienceNitrificationAlgorithm
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In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
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Hydroxy-Directed Enantioselective Hydroxyalkylation in the Carbocyclic Ring of Indoles

2017

[EN] A Cinchona-derived squaramide catalyzes the reaction between hydroxyindoles and isatins leading to enantioenriched indoles substituted in the carbocyclic ring. The reaction proceeds efficiently with differently substituted isatins, yielding the desired products with excellent regioselectivity, good yields, and high enantiocontroi. Moreover, every position of the carbocyclic ring of the indole can be functionalized by using the appropriate starting hydroxyindole. The OH group was removed smoothly upon hydrogenolysis of the corresponding triflate.

Indole test010405 organic chemistryChemistryStereochemistryOrganic ChemistryEnantioselective synthesisSquaramideRegioselectivity010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesReaccions químiquesCatàlisiHydrogenolysisFISICA APLICADAPhysical and Theoretical ChemistryTrifluoromethanesulfonateQuímica orgànica
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Synthesis of Functionalized Indoles with a Trifluoromethy-Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselective Friedel-Crafts Alk…

2010

[EN] Chiral complexes of BINOL-based ligands with zirconium tert-butoxide catalyze the Friedel-Crafts alkylation reaction of indoles with beta-trifluoromethyl-alpha,beta-unsaturated ketones to give functionalized indoles with an asymmetric tertiary carbon center attached to a trifluoromethyl group. The reaction can be applied to a large number of substituted alpha-trifluoromethyl enones and substituted indoles. The expected products were obtained with good yields and ees of up to 99%.

IndolesHydrocarbons FluorinatedAlkylationEnonesStereoisomerismAlkylationElectrophilic aromatic substitutionLigandsMedicinal chemistryCatalysisCatalysisStereocenterchemistry.chemical_compoundAsymmetric catalysisOrganic chemistryCombinatorial Chemistry TechniquesAromatic substitutionFriedel–Crafts reactionTrifluoromethylMolecular StructureChemistryOrganic ChemistryEnantioselective synthesisStereoisomerismGeneral ChemistryKetonesCarbonFISICA APLICADAZirconiumFluorinated compounds
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A homemade cytospin apparatus

2006

Information retrievalStaining and LabelingChemistryCytospin apparatusBiophysicsCentrifugationCell BiologyCell SeparationEquipment DesignMolecular BiologyBiochemistryBody Fluids
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Iron(II) Spin Transition Complexes with Dendritic Ligands, Part I

2008

The ligands G1- and G2-oligo (benzyl ether) (PBE) dendrons and their iron(II) complexes [Fe(Gn-PBE)3]A2·xH2O (with n = 1, 2 and A = triflate, tosylate) were prepared. The magnetic properties of the complexes were investigated by a SQUID magnetometer. All complexes exhibit gradual spin transition below room temperature. At very low temperatures the magnetic behaviour reflects zero-field splitting (ZFS) effects. 57Fe-Mossbauer spectroscopy was performed to distinguish between ZFS of high spin species and spin state conversion into the low spin state. Further characterisation was carried out by thermogravimetric analysis (TGA) and FT-IR spectroscopy. Structural features have been determined by…

Inorganic ChemistryCrystallographyThermogravimetric analysisSpin statesSpin crossoverStereochemistryChemistryMössbauer spectroscopySpin transitionSpectroscopyTrifluoromethanesulfonateMagnetic susceptibilityEuropean Journal of Inorganic Chemistry
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Synthesen mit substituierten Malondialdehyden, XI. γ‐Formyl‐tetramethinmerocyanin‐, γ‐Formyl‐pentamethincyanin‐ und [2.2.2]Heptamethincyanin‐Farbstof…

1972

Durch Kondensation des Formylmalondialdehyds (Triformylmethan) 5 mit heterocyclischen Imoniumsalzen 4 werden je nach Reaktionsbedingungen neuartige γ-Formyl-tetramethinmerocyanin-(6), γ-Formyl-pentamethincyanin-(8) und trinucleare symmetrische [2.2.2]Heptamethincyanin-Farbstoffe (9) dargestellt. Die Isolierung der Mono- (6) und Dikondensationsprodukte (8) des Formylmalondialdehyds ermoglicht die Darstellung unsymmetrischer Farbstoffe 8 und 9 mit verschiedenen Endgruppen. — Die trinuclearen [2.2.2]Heptamethincyanine 9 lassen sich in Analogie zu den phenylogen Guanidiniumionen (Triphenylmethanfarbstoffe) als methinyloge Guanidiniumkationen 3 (n = 3) auffassen. — Die spektroskopischen Eigensch…

Inorganic ChemistryReaction conditionschemistry.chemical_compoundTriphenylmethaneChemistryStereochemistrySpectral propertiesMedicinal chemistryTriformylmethaneChemische Berichte
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Der 1,3‐Dithian‐2‐ylmethoxycarbonyl‐(Dmoc)‐Rest als Zweistufen‐Schutzgruppe für die Aminofunktion von Aminosäuren und Peptiden

1982

Der 1,3-Dithian-2-ylmethoxycarbonyl-(Dmoc)-Rest (4) als Schutzgruppe fur die Aminofunktion ist gegen Basen und gegen Trifluoressigsaure stabil. Peptidsynthesen mit Dmoc-Aminosauren werden nach dem Mischanhydrid- und nach dem modifizierten Carbodiimid-Verfahren durchgefuhrt. Zur Abspaltung der Dmoc-Schutzgruppe wird diese mit Peressigsaure am Schwefel oxidiert (z. B. zu 13, 14). Die dabei gebildete CH-acide Form kann unter milden basischen Bedingungen von der blockierten Aminofunktion abgelost werden. The 1,3-Dithian-2-ylmethoxycarbonyl (Dmoc) Group as Two-Step Amino Protective Function in Peptide Chemistry The 1,3-dithian-2-ylmethoxycarbonyl (Dmoc) group (4) as amino protective function is …

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundChemistryStereochemistryTrifluoroacetic acidPeptide chemistryMoietyPeptideCarbodiimideChemische Berichte
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Formation and Reactivity of the [Cp‘2Ta(H)2]+ Cation (Cp‘ = η5-tBuC5H4)

1999

The complex Cp‘2Ta(H)(OCOCF3)2 (2) is synthesized by the acidolysis of Cp‘2TaH3 (1) (Cp‘ = η5-tBuC5H4) in the presence of an excess of trifluoroacetic acid. 1 undergoes a loss of H- upon the reacti...

Inorganic Chemistrychemistry.chemical_compoundChemistryOrganic ChemistryTrifluoroacetic acidReactivity (chemistry)Physical and Theoretical ChemistryMedicinal chemistryOrganometallics
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